TUMOUR-TARGETING PEPTIDE VARIANTS

Abstract

The present invention provides a peptide that selectively binds v6 integrin, the peptide having an amino acid sequence comprising the motif X.sub.1B.sub.nRGDLX.sub.2X.sub.3X.sub.4Z.sub.mX.sub.5, wherein X.sub.1 is any D-amino acid, B.sub.n is a sequence of any n amino acids, which may be natural or unnatural, D- or L-, and may be the same or different, wherein n is a number between 1 and 10, X.sub.2 and X.sub.3 are independently selected from any amino acid, X.sub.4 is Leu or Ile, Z.sub.m is a sequence of any m amino acids, which may be natural or unnatural, D- or L-, and may be the same or different, wherein m is a number between 1 and 10, X.sub.5 is any L- or D-amino acid. Also provided are conjugates comprising said peptide, pharmaceutical compositions comprising said peptide or said conjugates, and uses of said peptide, conjugate or composition, for example, in the treatment, imaging and/or diagnosis of an v6-expressing tumour in a mammalian subject.

Claims

1. A peptide that selectively binds v6 integrin, the peptide having an amino acid sequence comprising the motif X.sub.1B.sub.nRGDLX.sub.2X.sub.3X.sub.4Z.sub.mX.sub.5 (SEQ ID NO: 3), wherein X.sub.1 is any D-amino acid, B.sub.n is a sequence of any n amino acids, which may be natural or unnatural, D- or L-, and may be the same or different, wherein n is a number between 1 and 10, X.sub.2 and X.sub.3 are independently selected from any amino acid, X.sub.4 is Leu or Ile, Z.sub.m is a sequence of any m amino acids, which may be natural or unnatural, D- or L-, and may be the same or different, wherein m is a number between 1 and 10, X.sub.5 is any L- or D-amino acid.

2. The peptide according to claim 1, wherein the length of the peptide is between 17 and 25 amino acids, optionally wherein the length of the peptide is 20 amino acid.

3. The peptide according to claim 1 or claim 2, wherein X.sub.1 is D-Asn.

4. The peptide according to any one of the preceding claims, wherein X.sub.5 is L-Thr or D-Thr.

5. The peptide according to any one of the preceding claims, wherein X.sub.4 is Leu.

6. The peptide according to any one of the preceding claims, wherein n is 5 and/or m is 6.

7. The peptide according to any one of the preceding claims, wherein B.sub.n is AVPNL (SEQ ID NO: 4), KVPNL (SEQ ID NO: 5) or K (biotin) VPNL.

8. The peptide according to any one of the preceding claims, wherein Z.sub.m is AQKVAR (SEQ ID NO: 6).

9. The peptide according to any one of the preceding claims, wherein the amino acid sequence of the peptide is selected from the group consisting of: TABLE-US-00032 (SEQIDNO:7) H.sub.2N-[D-Asn]-AVPNLRGDLQVLAQKVART-COOH; (SEQIDNO:8) H.sub.2N-[D-Asn]-KVPNLRGDLQVLAQKVART-COOH; (SEQIDNO:8) H.sub.2N-[D-Asn]-K(biotin)VPNLRGDLQVLAQKVART-COOH; (SEQIDNO:9) H.sub.2N-[D-Asn]-KVPNLRGDLQVLAQKVAR[D-Thr]-COOH; (SEQIDNO:9) H.sub.2N-[D-Asn]-K(biotin)VPNLRGDLQVLAQKVAR[D-Thr]-COOH; and (SEQIDNO:10) H.sub.2N-[D-Asn]-AVPNLRGDLQVLAQKVAR[D-Thr]-COOH.

10. The peptide according to claim 9, wherein the peptide is H.sub.2N-[D-Asn]-AVPNLRGDLQVLAQKVART-COOH (SEQ ID NO: 7).

11. The peptide according to any one of the preceding claims, wherein the peptide is N-acetylated and/or C-amidated.

12. A conjugate comprising a peptide as defined in any one of claims 1 to 11 conjugated directly or via a linker to a therapeutic moiety, a polymer, a polypeptide and/or a detectable moiety.

13. The conjugate according to claim 12, wherein the therapeutic moiety comprises an anti-cancer agent.

14. The conjugate according to claim 13, wherein the anti-cancer agent is selected from the group consisting of: an auristatin, a maytansinoids, a tubulysin, duocarmycin, calicheamicin, alpha-amanitin, a pyrrolobenzodiazepine, irinotecan, and an indolecarboxamide, or an analogue, derivatives, prodrug or active metabolite thereof.

15. The conjugate according to claim 14, wherein the anti-cancer agent comprises: Monomethyl Auristatin E (MMAE), mertansine (DM1), ravtansine (DM4) or Centanamycin.

16. The conjugate according to any one of claims 12 to 15, wherein the therapeutic moiety comprises a radioactive isotope selected from the group consisting of: .sup.177Lu, .sup.90Y, .sup.211At, .sup.213Bi, .sup.212Pb, .sup.225Ac, .sup.223Ra, .sup.44Sc, .sup.67Ga, .sup.131I, .sup.188Re, .sup.186Re and .sup.67Cu.

17. The conjugate according to any one of claims 12 to 16, wherein the detectable moiety is detectable by Magnetic Resonance Imaging (MRI), Magnetic Resonance Spectroscopy (MRS), Single Photon Emission Computed Tomography (SPECT), Positron Emission Tomograph (PET) or optical imaging.

18. The conjugate according to claim 17, wherein the detectable moiety comprises a fluorophore, a radionuclide or a spin label.

19. The conjugate according to claim 18, wherein the detectable moiety comprises: .sup.68Ga, IRDye 700, IRDye 800, Fluorescein isothiocyanate (FITC), .sup.89Zr, .sup.124I, .sup.64Cu, .sup.62Cu, .sup.18F, .sup.86Y, .sup.111In, .sup.131I, .sup.123I, .sup.67Ga or .sup.99mTc.

20. The conjugate according to any one of claims 12 to 19, wherein the detectable moiety comprises .sup.111In coupled to the peptide via a linker that comprises a chelator, optionally wherein the chelator comprises diethylenetriamine pentaacetic acid (DTPA), tetrazacyclododecane-1,4,7,10-tetraacetic acid (DOTA) or ethylenediaminetetraacetic acid (EDTA).

21. The conjugate according to any one of claims 12 to 20, wherein the polymer comprises one or more (e.g. one or two) ethylene glycol groups or one or more (e.g. one or two) polyethylene glycol (PEG) chains.

22. The conjugate according to claim 21, wherein the one or more (e.g. one or two) PEG chains are between 1 and 50 ethylene glycol units in length.

23. A pharmaceutical composition comprising: a peptide as defined in any one of claims 1 to 11 or a conjugate as defined in any one of claims 12 to 22; and a pharmaceutically acceptable carrier.

24. A peptide as defined in any one of claims 1 to 11, a conjugate as defined in any one of claims 12 to 22 or a pharmaceutical composition as defined in claim 23 for use in medicine.

25. A peptide as defined in any one of claims 1 to 11, a conjugate as defined in any one of claims 12 to 22 or a pharmaceutical composition as defined in claim 23 for use in a method of treatment of an v6-expressing tumour in a mammalian subject.

26. The peptide, conjugate or composition for use according to claim 25, wherein the tumour is a cervical tumour, a head or neck tumour, a breast tumour, a lung tumour, a skin tumour, a colon tumour, an ovarian tumour or a pancreatic tumour.

27. A method of treating a mammalian subject having an v6-expressing tumour, the method comprising administering a therapeutically effective amount of a peptide as defined in any one of claims 1 to 11, a conjugate as defined in any one of claims 12 to 22 or a pharmaceutical composition as defined in claim 23 to the subject in need thereof.

28. The method according to claim 27, wherein the tumour is a cervical tumour, a head or neck tumour, a breast tumour, a lung tumour, a skin tumour, a colon tumour, an ovarian tumour or a pancreatic tumour.

29. Use of a peptide as defined in any one of claims 1 to 11, a conjugate as defined in any one of claims 12 to 22 or a pharmaceutical composition as defined in claim 23 in the preparation of a medicament for the treatment of an v6-expressing tumour in a mammalian subject.

30. Use according to claim 29, wherein the tumour is a cervical tumour, a head or neck tumour, a breast tumour, a lung tumour, a skin tumour, a colon tumour, an ovarian tumour or a pancreatic tumour.

31. A method of imaging an v6-expressing tumour in a mammalian subject comprising administering a conjugate as defined in any one of claims 17 to 22 to the tumour-bearing subject and detecting said detectable moiety thereby forming an image of said tumour.

32. The method according to claim 31, wherein the tumour is a cervical tumour, a head or neck tumour, a breast tumour, a lung tumour, a skin tumour, a colon tumour, an ovarian tumour or a pancreatic tumour.

33. A conjugate as defined in any one of claims 17 to 22 for use in an in vivo method of diagnosis of cancer in a mammalian subject, wherein the method comprises administering the conjugate to the subject and detecting said detectable moiety thereby diagnosing the presence of an v6-expressing tumour in the subject.

34. A method of cancer diagnosis comprising administering a conjugate as defined in any one of claims 17 to 22 to a mammalian subject suspected of having an v6-expressing tumour and detecting said detectable moiety thereby diagnosing the presence of an v6-expressing tumour in the subject.

Description

BRIEF DESCRIPTION OF THE FIGURES

[0043] FIG. 1 shows the structures of the non-proteinogenic amino acids used for the synthesis of peptides 2-15.

[0044] FIG. 2 shows a comparison of peptide 22 to peptide 25 testing in vitro. All A20FMDV2 variants were screened for specificity, activity and internalisation. A) Specificity is the absence of binding to A375Puro at 1000 nM (upper histograms) and binding only to A375P6 (lower histograms) and the shift of the histogram shows the Geometric Mean (GM) of the Mean Fluorescent Intensity (MFI) via flow cytometry at the same concentration of 100 nM shown by Ai) Peptide 22 (left-hand histograms) and Aii) peptide 25 (right-hand histograms). B) Affinity was determined by measuring the level of binding to A375P6 at 0.1, 1, 10, 100 and 1000 nM via flow cytometry. The results show the binding of the peptides relative to the commercially sourced control biotinylated-A20FMDV2. Data from a single representative experiment shows that Bii) peptide 25 (right-hand graph) binds better to A375P6 at similar concentrations compared to Bi) peptide 22 (left-hand graph). C) Internalisation shows v6-dependent internalisation by A375P6 cells using Imagestream. Data shows the peptide at the surface of the cell (green, right-hand side images in each panel) at 0 minutes and after 45 minutes Ci) peptide 22 and Cii) peptide 25 have been internalised and they have a similar rate of internalisation (see graphs below the images; peptide 22 left-hand graph, peptide 25 right-hand graph).

[0045] FIG. 3 shows the stability of peptides in human plasma (n=2) and PBS (control) after 24 h. Peptide 22, 25 and 26 are over 75% stable in plasma, in comparison to the peptide 23 and 24 that are less than 50% stable. Peptide levels were quantified using liquid chromatography-mass spectrometry (LC-MS). the stability of peptides in human plasma (labelled blood, right-hand bars for each peptide) and PBS (left-hand bars for each peptide) determined after 24 hours. In this experiment, PBS was used as a control.

[0046] FIG. 4 shows the uptake of .sup.111In-DTPA coupled peptides in positive v6-expressing tumour and negative control tumour (A375Puro). The peptides are specifically taken into v6-expressing tumour (blue; right-hand bars for each peptide) compared to the negative tumour (red; left-hand bars for each peptide). The relative uptake is shown by the ratio A375Puro:A3756. The data show that 25 is almost 10 times more specific to v6-expressing tumour compared to the negative tumour. The data are plotted as mean Injected Dose (ID) per gram of tissueStandard Error of the Mean (SEM) for each of peptides 22-26.

DETAILED DESCRIPTION OF THE INVENTION

[0047] In describing the present invention, the following terms will be employed, and are intended to be defined as indicated below.

[0048] Peptide Variants and Unnatural Amino Acids

[0049] As defined herein, the peptides of the present invention are variants of the parent A20FMDV2 peptide and may comprise one or more unnatural amino acids, provided that the peptide is as defined in the claims. Suitable unnatural amino acids include, for example, D-amino acids, ornithine, diaminobutyric acid ornithine, norleucine ornithine, pyriylalanine, thienylalanine, naphthylalanine, phenylglycine, alpha and alpha-disubstituted amino acids, N-alkyl amino acids, lactic acid, halide derivatives of natural amino acids, such as trifluorotyrosine, p-Cl-phenylalanine, p-Br-phenylalanine, p-I-phenylalanine, L-allyl-glycine, b-alanine, L-a-amino butyric acid, L-g-amino butyric acid, L-a-amino isobutyric acid, L-e-amino caproic acid, 7-amino heptanoic acid, L methionine sulfone, L-norleucine, L-norvaline, p-nitro-L-phenylalanine, L-hydroxyproline, L-thioproline, methyl derivatives of phenylalaninesuch as 1-methyl-Phe, pentamethyl-Phe, L-Phe(4-amino), L-Tyr(methyl), L-Phe(4-isopropyl), L-Tic(1,2,3,4-tetrahydroisoquinoline-3-carboxyl acid), L-diaminopropionic acid and L-Phe(4-benzyl). The peptides may be further modified. For example, one or more amide bonds may be replaced by ester or alkyl backbone bonds. There may be N or C alkyl substituents, side chain modifications or constraints such as disulphide bridges, side chain amide or ester linkages.

[0050] The peptides of the present invention may include both modified peptides and synthetic peptide analogues. Peptides may be, for example, be modified to improve formulation and storage properties, or to protect labile peptide bonds by incorporating non-peptidic structures.

[0051] The peptides of the present invention may include an N-terminal and/or C-terminal modification. For example, N-terminal acetylation and/or C-terminal amidation.

[0052] Peptides of the present invention may be prepared using methods known in the art. For example, peptides may be produced by chemical synthesis, e.g. solid phase techniques and automated peptide synthesisers, or by recombinant means (using nucleic acids such as those described herein). For example, peptides may be synthesised using solid phase strategies on an automated multiple peptide synthesizer (Abimed AMS 422) using 9-fluorenylmethyloxycarbonyl (Fmoc) chemistry. The peptides can then be purified by reversed phase-HPLC and lyophilized. Particular synthesis methods for making peptides of the invention are described in the Examples below.

[0053] In some cases X.sub.2 and X.sub.3 are helix promoting residues. In some cases the Z.sub.m amino acids are helix promoting residues. As used herein, the helix promoting residues may be independently selected from the group consisting of Glu, Ala, Leu, Met, Gln, Lys, Arg, Val, Ile, Trp, Phe and Asp. The helix promoting residues may include one or more artificial or modified amino acids.

[0054] Detectable Moiety

[0055] As used herein, the peptide of the present invention may be conjugated to a detectable moiety. The term detectable moiety relates to a moiety which, when located at the target site following administration of the conjugates of the invention into a patient, may be detected, typically non-invasively from outside the body and the site of the target located. Thus, the conjugates of this embodiment of the invention are useful in imaging and diagnosis. Readily detectable moieties are entities that are detectable by imaging techniques such as Magnetic Resonance Imaging (MRI), Magnetic Resonance Spectroscopy (MRS), Single Photon Emission Computed Tomography (SPECT) and Positron Emission Tomography (PET) and optical imaging. Preferably, imaging moieties are stable, non-toxic entities that retain their properties under in vitro and in vivo conditions. Examples of such moieties include but are not limited to radioactive moieties, for example radioactive isotopes. Suitable radioactive atoms include indium-111, technetium-99m or iodine-123 for scintigraphic studies. Other readily detectable moieties include, for example, spin labels for MRI such as iodine-123, iodine-131, indium-111, fluorine-18, carbon-13, nitrogen-15, oxygen-17, gadolinium, manganese or iron and optical moieties which include Cy5.5 and quantum dots. Further examples of detectable moieties include .sup.68Ga, IRDye 700, IRDye 800, Fluorescein isothiocyanate (FITC), .sup.89Zr, .sup.124I, .sup.64Cu, .sup.62Cu, .sup.18F, .sup.86Y, .sup.111In, .sup.131I, .sup.123I, .sup.67Ga and .sup.99mTc.

[0056] The term therapeutic moiety encompasses a moiety having beneficial, prophylactic and/or therapeutic properties.

[0057] Cytotoxic chemotherapeutic agents are well known in the art and include anti-cancer agents such as:

[0058] Alkylating agents including nitrogen mustards such as mechlorethamine (HN2), cyclophosphamide, ifosfamide, melphalan (L-sarcolysin) and chlorambucil; 10 ethylenimines and methylmelamines such as hexamethylmelamine, thiotepa; alkyl sulphonates such as busulfan; nitrosoureas such as carmustine (BCNU), lomustine (CCNLJ), semustine (methyl-CCN-U) and streptozoein (streptozotocin); and triazenes such as decarbazine (DTIC; dimethyltriazenoimidazolecarboxamide); Antimetabolites including folic acid analogues such as methotrexate (amethopterin); pyrimidine analogues such as fluorouracil (5-fluorouracil; 5-FU), floxuridine (fluorodeoxyuridine; FUdR) and cytarabine (cytosine arabinoside); and purine analogues and related inhibitors such as mercaptopurine (6-mercaptopurine; 6-MP), thioguanine (6-thioguanine; TG) and pentostatin (2-deoxycofonnycin). Natural Products including vinca alkaloids such as vinblastine (VLB) and vincristine; epipodophyllotoxins such as etoposide and teniposide; antibiotics such as dactinomycin (actinomycin D), daunorabicin (daunomycin; rubidomycin), doxorubicin, bleomycin, plicamycin (mithramycin) and mitomycin (mitomycin Q; enzymes such as L-asparaginase; and biological response modifiers such as interferon alphenomes. Miscellaneous agents including platinum coordination complexes such as cisplatin (cis-DDP) and carboplatin; anthracenedione such as mitoxantrone and antbracycline; substituted urea such as hydroxyurea; methyl hydrazine derivative such as procarbazine (N-methylhydrazine, MIH); and adrenocortical suppressant such as mitotane (o, p-DDD) and aminoglutethimide; taxol and analogues/derivatives; and hormone agonists/antagonists such as flutamide and tamoxifen.

[0059] In particular, the peptide of the invention may be conjugated to an anti-cancer agent selected from an auristatin, a maytansinoids, a tubulysin, duocarmycin, calicheamicin, alpha-amanitin, a pyrrolobenzodiazepine (PBD), irinotecan, and an indolecarboxamide, or an analogue, derivatives, prodrug or active metabolite thereof. Specific examples include: Monomethyl Auristatin E (MMAE), mertansine (DM1), ravtansine (DM4) and Centanamycin.

[0060] In certain cases, the anti-cancer agent may be a cytotoxic peptide or polypeptide moiety by which we include any moiety which leads to cell death.

[0061] Cytotoxic peptide and polypeptide moieties are well known in the art and include, for example, ricin, abrin, Pseudomonas exotoxin, tissue factor and the like.

[0062] The use of ricin as a cytotoxic agent is described in Burrows & Thorpe, P.N.A.S. USA 90: 8996-9000, 1993, incorporated herein by reference, and the use of tissue factor, which leads to localised blood clotting and infarction of a tumour, has been described by Ran et al, Cancer Res. 58: 4646-4653, 1998 and Huang et al, Science 275: 25 547-550, 1997. Tsai et al, Dis. Colon Rectum 38: 1067-1074, 1995 describes the abrin A chain conjugated to a monoclonal antibody and is incorporated herein by reference. Other ribosome inactivating proteins are described as cytotoxic agents in WO 96/06641. Pseudomonas exotoxin may also be used as the cytotoxic polypeptide moiety (see, for example, Aiello et al, P.N.A.S. USA 92: 10457-10461, 1995.

[0063] Certain radioactive atoms may also be cytotoxic if delivered in sufficient doses. Thus, the anti-cancer agent may comprise a radioactive atom which, in use, delivers a sufficient quantity of radioactivity to the target site so as to be cytotoxic. Suitable radioactive atoms include phosphorus-32, iodine-125, iodine-131, indium-111, rhenium-186, rhenium-188, astatine-211 or yttrium-90, or any other isotope which emits enough energy to destroy neighbouring cells, organelles or nucleic acid. In particular, the therapeutic radioactive isotope may be selected from the group consisting of: .sup.177Lu, .sup.90Y, .sup.211At, .sup.213Bi, .sup.212Pb, .sup.225Ac, .sup.223Ra, .sup.44Sc, .sup.67Ga, .sup.131I, .sup.188Re, .sup.186Re and .sup.67Cu. Preferably, the isotopes and density of radioactive atoms in the compound of the invention are such that a dose of more than 4000 cGy, and more preferably at least 6000, 8000 or 10000 cGy, is delivered to the target site and, preferably, to the cells at the target site and their organelles, particularly the nucleus. The radioactive atom may be attached to the binding moiety in known ways. For example, EDTA, DTPA, DOTA or another chelating agent may be attached to the peptide of the invention and used to attach metal radionuclides including .sup.111In, .sup.68Ga, .sup.90Y or radioactive atoms as described above. Tyrosine residues may introduced into the peptide of the invention and may be labelled with .sup.125I or .sup.131I.

[0064] Methods of conjugating peptides to therapeutic agents are well known in the art. These may include use of linkers, for example cleavable linkers.

[0065] The term pharmaceutically acceptable carrier generally includes components that are compatible with the peptide or conjugate thereof and are not deleterious to the recipients thereof. Typically, the carriers will be water or saline which will be sterile and pyrogen free; however, other acceptable carriers may be used. Typically the pharmaceutical compositions or formulations of the invention are for parenteral administration, more particularly for intravenous administration.

[0066] The medicament or pharmaceutical composition of the present invention as defined above may usefully be administered to a patient who is also administered other medicaments, as it will be known to those skilled in the art. For example, in the case of cancer, the medicament or pharmaceutical composition of the present invention may be administered to a patient before, after or during administration of the other anti-tumour agent(s), for example before, after or during chemotherapy. Treatment with the peptide after chemotherapy may be particularly useful in reducing or preventing recurrence of the tumour or metastasis. For example, the anti-tumour agent can be covalently linked directly or indirectly to a peptide of the invention.

[0067] Determining v6 Expression

[0068] The skilled person will be aware of numerous techniques for determining whether a sample (such as a tumour sample) expresses the integrin v6. In particular embodiments, the subject to be treated may have a tumour having one or more cells that express the integrin v6. In certain cases, the finding that the tumour expresses the integrin v6 (i.e. that it is an v6-positive cancer) may have been carried out previously or may be inferred from the type of cancer. For example, a number of tumour types are known to express the integrin v6, including a cervical tumour, a head or neck tumour, a breast tumour, a lung tumour, a skin tumour, a colon tumour, an ovarian tumour or a pancreatic tumour. Without wishing to be bound by any particular theory, the present inventors believe cancers of the gastrointestinal (GI) tract and carcinomas that develop from many epithelial tissues may benefit from v6-targeting therapy using a peptide or conjugate of the present invention. As the range of cancers found to express v6 expands through additional research effort, so the range of cancers that may exhibit therapeutic benefit from v6-targeting therapy using a peptide or conjugate of the present invention is expected to grow.

[0069] Additionally or alternatively, in certain cases the treatment may involve an active step of determining whether the tumour expresses the integrin v6. Such a step may, for example, be carried out prior to initiating treatment with an v6-targeting peptide or conjugate of the present invention in order to predict the likely suitability of the subject for therapy using an v6-targeting peptide or conjugate of the present invention. Determining v6 expression may involve measuring protein expression and/or level in a tumour sample using immunohistochemistry, measuring protein levels in a cell lysate by ELISA or Western blotting, and/or using a binding agent capable of specifically binding to v6 or a fragment or subunit thereof.

[0070] In certain embodiments, determining whether the subject has an v6-positive cancer may be performed on a nucleic acid extracted from a sample of cells obtained from the cancer, from a sample of cancer cells circulating in blood and/or from circulating tumour DNA (ctDNA) in blood or plasma.

[0071] In certain cases, determining the expression of v6 comprises extracting RNA from a sample of cancer cells and measuring expression by real time PCR and/or by using a probe capable of hybridising to RNA encoding v6 or a fragment thereof. The presence or amount of v6 integrin may be determined directly using a binding agent, such as an antibody or a peptide or conjugate of the present invention, which is capable of specifically binding to v6, or a fragment thereof. The binding agent may be labelled to enable it to be detected or capable of detection following reaction with one or more further species, for example using a secondary antibody that is labelled or capable of producing a detectable result, e.g. in an ELISA type assay.

[0072] Samples

[0073] A test sample as used herein may be a cell or tissue sample (e.g. a biopsy), a biological fluid, an extract (e.g. a protein or DNA extract obtained from the subject). In particular, the sample may be a tumour sample, a blood sample (including plasma or serum sample), a cerebrospinal fluid sample, or a non-tumour tissue sample. The sample may be one which has been freshly obtained from the subject or may be one which has been processed and/or stored prior to making a determination (e.g. frozen, fixed or subjected to one or more purification, enrichment or extractions steps). Techniques for enriching a blood or plasma sample for circulating tumour DNA (e.g. based on fragment size) have been described. Moreover, sequencing techniques for identifying cancer-associated mutations in ctDNA have been described (e.g. based on digital PCR, targeted deep sequencing, nested real-time PCR, and the like).

[0074] And/or where used herein is to be taken as specific disclosure of each of the two specified features or components with or without the other. For example A and/or B is to be taken as specific disclosure of each of (i) A, (ii) B and (iii) A and B, just as if each is set out individually herein.

[0075] The features disclosed in the foregoing description, or in the following claims, or in the accompanying drawings, expressed in their specific forms or in terms of a means for performing the disclosed function, or a method or process for obtaining the disclosed results, as appropriate, may, separately, or in any combination of such features, be utilised for realising the invention in diverse forms thereof.

[0076] While the invention has been described in conjunction with the exemplary embodiments described above, many equivalent modifications and variations will be apparent to those skilled in the art when given this disclosure. Accordingly, the exemplary embodiments of the invention set forth above are considered to be illustrative and not limiting. Various changes to the described embodiments may be made without departing from the spirit and scope of the invention. For the avoidance of any doubt, any theoretical explanations provided herein are provided for the purposes of improving the understanding of a reader. The inventors do not wish to be bound by any of these theoretical explanations.

[0077] Any section headings used herein are for organizational purposes only and are not to be construed as limiting the subject matter described.

[0078] Throughout this specification, including the claims which follow, unless the context requires otherwise, the word comprise and include, and variations such as comprises, comprising, and including will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps. It must be noted that, as used in the specification and the appended claims, the singular forms a, an, and the include plural referents unless the context clearly dictates otherwise. Ranges may be expressed herein as from about one particular value, and/or to about another particular value. When such a range is expressed, another embodiment includes from the one particular value and/or to the other particular value. Similarly, when values are expressed as approximations, by the use of the antecedent about, it will be understood that the particular value forms another embodiment. The term about in relation to a numerical value is optional and means for example +/10%.

[0079] The following is presented by way of example and is not to be construed as a limitation to the scope of the claims.

EXAMPLES

[0080] To enable binding activity to the v6 integrin by flow cytometry to be measured, all peptides were synthesised incorporating a .sup.2Lys(D-biotin) residue instead of native Ala (i.e. A20FMDV2, as disclosed in WO2007/039728, has Ala at position 2). For comparison we compared our own SPPS synthesized peptides with commercially synthesized biotinylated-A20FMDV2 (called biotinylated-A20FMDV2-A in Table 2 below). Following activity studies, biotinylated peptides exhibiting potent binding activity were then selected and the metal chelator diethylenetriamine pentaacetic acid (DTPA) [17] was incorporated to facilitate coupling of .sup.111In for plasma stability studies and in vivo biodistribution studies. The synthesis, binding studies and plasma stability of biotinylated A20FMDV2, its non-proteinogenic derivatives, and biotinylated and DPTA-incorporated analogues, are described in detail below.

Experimental

[0081] General Information

[0082] All reagents were purchased as reagent grade and used without further purification. HPLC solvents were purchased as HPLC grade and used without further purification. FmocNH-L-Thr(.sup.tBu)-OCH.sub.2-phi-OCH.sub.2CH.sub.2CO.sub.2H was purchased from PolyPeptide (Strasbourg, France). O-(Benzotriazol-1-yl)-N,N,N,N-tetramethyluronium hexafluoro phosphate (HBTU), O-(7-azabenzotriazol-1-yl)-N,N,N,N-tetramethyluronium hexafluorophosphate (HATU), Rink amide, 4-(hydroxymethyl)phenoxyacetic acid (HMP), Boc anhydride and N,N-diisopropylcarbodiimide (DIC) were purchased from GL Biochem (Shanghai, China). N,N-dimethylformamide (DMF) (AR grade) and acetonitrile (CH.sub.3CN) (HPLC grade) were purchased from Scharlau (Barcelona, Spain). Diisopropylethylamine (.sup.iPr.sub.2NEt), 4-dimethylaminopyridine (DMAP), piperidine, N-methyl-2-pyrrolidone (NMP), collidine, 1,8-diazabicycloundec-7-ene (DBU), 2-mercaptoethanol, triisopropylsilane (TIPS) and 3,6-dioxa-1,8-octanedithiol (DODT) were purchased from Sigma-Aldrich (St Louis, Mo.). 2-Nitrobenzenesulfonyl chloride (2-NBS-Cl) and dimethylsulfate (DMS) were obtained from AK Scientific (Union City, Calif.). Trifluoroacetic acid (TFA) was purchased from Oakwood Chemicals (River Edge City, Calif.). The aminomethyl polystyrene resin and DTPA was synthesised according to published procedures [21, 22]. Fmoc-amino acids were purchased from GL Biochem with the following side chain protection: Fmoc-Arg(Pbf)-OH (Pbf=2,2,4.6,7-pentamethyldihydrobenzofuran-5-sulfonyl), Fmoc-Asn(Trt)-OH (Trt=triphenylmethyl), Fmoc-Asp(.sup.tBu)-OH (.sup.tBu=tert-butyl), Fmoc-Gln(Trt)-OH, Fmoc-Glu(.sup.tBu)-OH, Fmoc-Lys(Boc)-OH, Fmoc-D-Lys(Boc)-OH, Fmoc-Orn(Boc)-OH, Fmoc-Dab(Boc)-OH, Fmoc-Dap(Boc)-OH, Fmoc-D-Thr(.sup.tBu)-OH and Fmoc-D-Asn(Trt)-OH.

[0083] Electrospray ionisation mass spectra (ESI-MS) were recorded on an Agilent Technologies (Santa Clara, Calif.) 1120 Compact LC connected to an in-line Hewlett Packard (Palo Alto, Calif.) 1100MSD spectrometer. Samples were introduced using direct flow injection at 0.2 mL/min into an ESI source in positive mode, using 0.1% formic acid/H.sub.2O and 0.1% formic acid/CH.sub.3CN (1:1, v/v). Major and significant fragments were quoted in the form x m/z (mass to charge ratio). Analytical RP-HPLC was performed on an Ultimate 3000 system using a Waters XTerra C18 column (5 m, 4.6150 mm) at a flow rate of 1 mL/min. A linear gradient of 0.1% TFA/H.sub.2O (solvent A) and 0.1% TFA/CH.sub.3CN (solvent B) was used with detection at 210 nm. Preparative RP-HPLC was performed on a Waters 600 System with a Waters 2487 dual wavelength absorbance detector using a Waters XTerra Prep MS C18 column (10 m, 19300 mm) at a flow rate of 10 mL/min. Gradient systems were adjusted according to the elution profiles and peak profiles obtained from the analytical RP-HPLC chromatograms.

[0084] General Peptide Synthesis Procedure

[0085] Solid phase peptide synthesis (0.1 mmol scale) was performed on aminomethyl polystyrene resin (0.8 mmol/g) based on the Fmoc chemistry strategy. FmocNH-L-Thr (.sup.tBu)-OCH.sub.2-phi-OCH.sub.2CH.sub.2CO.sub.2H was attached to the resin using general method A (see below), Rink amide was attached to the resin using general method B, and HMP was coupled to the resin using general method C [20]. Coupling of Fmoc-D-Thr(.sup.tBu)-OH was achieved using general method D. The desired peptide sequences were synthesised either manually or on a Tribute (Tucson, Ariz.) peptide synthesiser using general method E, peptide bond N-methylation was carried out using general method F,[19] and coupling of Fmoc-Gln(Trt)-OH to N-methylated lysine was carried out using general method G. N-Terminal acetylation was carried out using general method H, and tert-butyl protected DTPA was coupled to the peptides using general method I. D-Biotin was attached to the peptides using general method J. The linear peptides were cleaved from the resin using general method K, and the crude products were purified according to general method L.

[0086] General Method A: Attachment of FmocNH-L-Thr(.sup.tBu)-OCH.sub.2-Phi-OCH.sub.2CH.sub.2CO.sub.2H to Aminomethyl Polystyrene Resin

[0087] Aminomethyl polystyrene resin (0.1 mmol) was swollen in CH.sub.2Cl.sub.2/DMF (1:1, v/v) for 20 minutes and the solvent was removed by filtration. To the resin was added a solution of FmocNH-L-Thr(.sup.tBu)-OCH.sub.2-phi-OCH.sub.2CH.sub.2CO.sub.2H (2 eq.) in 10% DMF/CH.sub.2Cl.sub.2 (1 mL, v/v) followed by DIC (2 eq.), and the reaction mixture was agitated at room temperature for 3 hours. The solution was drained, and the resin was washed with DMF (35 mL), CH.sub.2Cl.sub.2 (35 mL) and air dried to give 16. A negative Kaiser test [41] indicated complete reaction.

[0088] General Method B: Attachment of Rink Amide to Aminomethyl Polystyrene Resin

[0089] Aminomethyl polystyrene resin (0.1 mmol) was swollen in CH.sub.2Cl.sub.2/DMF (1:1, v/v) for 20 minutes and the solvent was removed by filtration. To the resin was added a solution of Rink amide (2 eq.) in 10% DMF/CH.sub.2Cl.sub.2 (1 mL, v/v) followed by DIC (2 eq.), and the reaction mixture was agitated at room temperature for 3 hours. The solution was drained, and the resin was washed with DMF (35 mL), CH.sub.2Cl.sub.2 (35 mL) and air dried. A negative Kaiser test indicated complete reaction.

[0090] General Method C: Attachment of 4-(Hydroxymethyl)Phenoxyacetic Acid (HMP) to Aminomethyl Polystyrene Resin (Synthesis of Resin 27)

[0091] Aminomethyl polystyrene resin (0.1 mmol) was swollen in CH.sub.2Cl.sub.2/DMF (1:1, v/v) for 20 minutes and the solvent was removed by filtration. To the resin was added a solution of HMP (2 eq.) in 10% DMF/CH.sub.2Cl.sub.2 (1 mL, v/v) followed by DIC (2 eq.), and the reaction mixture was agitated at room temperature for 3 hours. The solution was drained, and the resin was washed with DMF (35 mL), CH.sub.2Cl.sub.2 (35 mL) and air dried to give 27. A negative Kaiser test indicated complete reaction.

[0092] General Method D: Attachment of Fmoc-D-Thr(.sup.tBu)-OH to HMP-Resin 27

[0093] To the resin was added a solution of Fmoc-D-Thr(.sup.tBu)-OH (2 eq.) in DMF (1 mL) and DIC (2 eq.) followed by dropwise addition of DMAP (10% eq.) in DMF (100 L). The reaction mixture was agitated at room temperature for 2 hours. After the solution was drained and the resin washed with DMF (35 mL), esterification was repeated for further 2 hours. To the resin was added 20% acetic anhydride/DMF (1 mL) and a solution of DMAP (10% eq.) in DMF (100 L) dropwise, and the reaction mixture was agitated at room temperature for 1 hour after which the solution was drained and the resin washed with DMF (35 mL).

[0094] General Method E: Manually and Automated Fmoc SPPS

[0095] To a solution of Fmoc protected amino acid (5 eq.) in DMF (1 mL) was added HBTU (4.75 eq.) and .sup.iPr.sub.2NEt (10 eq.), and the solution was added to the resin. After agitating the mixture at room temperature for 30 minutes, the solution was drained and the resin was washed with DMF (35 mL). The Fmoc protecting group was removed by treatment with 20% piperidine/DMF (5 mL, v/v) at room temperature for 5 minutes then 10 minutes.

[0096] General Method F: Peptide Bond N-Methylation

[0097] NBS protection: To a solution of 2-NBS-Cl (4 eq.) in NMP (1 mL) was added collidine (10 eq.), and the solution was added to the resin and the reaction mixture agitated at room temperature for 15 minutes. After the solution was drained and the resin washed with NMP (35 mL), the reaction was repeated for further 10 minutes. N-methylation: To the resin was added a solution of DBU (3 eq.) in NMP (1 mL), and the reaction mixture was agitated at room temperature for 3 minutes. A solution of DMS (10 eq.) in NMP (1 mL) was then added to the reaction mixture, and the reaction mixture was agitated at room temperature for 2 minutes. After the solution was drained and the resin washed with NMP (35 mL), the reaction was repeated for further 2 minutes. NBS deprotection: To the resin was added a solution of 2-mercaptoethanol (10 eq.) and DBU (5 eq.) in NMP (2 mL), and the reaction mixture was agitated at room temperature for 5 minutes. After the solution was drained and the resin washed with NMP (35 mL), the reaction was repeated for further 5 minutes.

[0098] General Method G: Coupling of Fmoc-Gln(Trt)-OH to N-Methylated Lys

[0099] To a solution of Fmoc-Gln(Trt)-OH (5 eq.) in DMF (1 mL) was added HATU (4.75 eq.) and .sup.iPr.sub.2NEt (10 eq.), and the solution was added to the resin and the reaction mixture agitated at room temperature for 3 hours. After the solution was drained and the resin washed with DMF (35 mL), the reaction was repeated for further 3 hours.

[0100] General Method H: N-Terminal Acetylation

[0101] To the resin was added a solution of 20% acetic anhydride/DMF (1 mL), followed by dropwise addition of a solution of DMAP (10% eq.) in DMF (100 L). After the reaction mixture was agitated at room temperature for 30 minutes, the solution was drained, and the resin was washed with DMF (35 mL).

[0102] General Method I: Attachment of Tert-Butyl Protected DTPA

[0103] To a solution of 42 (5 eq.) in DMF (1 mL) was added HBTU (4.75 eq.) and .sup.iPr.sub.2NEt (10 eq.), and the solution was added to the resin. After agitating the mixture at room temperature for 30 minutes, the solution was drained and the resin was washed with DMF (35 mL).

[0104] General Method J: Attachment of D-Biotin

[0105] For the synthesis of peptides 1-15, and peptides 17, 19, 20 and 21, the N-terminal Fmoc group was removed by treatment with 20% piperidine/DMF (5 mL, v/v) at room temperature for 5 minutes then 10 minutes. After washing with DMF (35 mL), a solution of (Boc).sub.2O (5 eq.) in DMF (1 mL) was added to the resin, and the reaction mixture was agitated at room temperature for 30 minutes then washed with DMF (35 mL). The Dde group was removed by using 2% hydrazine/DMF (5 mL, v/v) at room temperature for 5 minutes and repeated with fresh reagents for 10 minutes. After washing with DMF (35 mL), a solution of D-biotin (5 eq.), HBTU (4.75 eq.) and .sup.iPr.sub.2NEt (10 eq.) in DMF (1 mL) was added to the resin, and the reaction mixture was agitated at room temperature for 30 minutes then washed with DMF (35 mL).

[0106] For the synthesis of peptides 16 and 18 and peptides 22-26, the Dde group was removed using 2% hydrazine/DMF (5 mL, v/v) at room temperature for 5 minutes and repeated with fresh reagents for 10 minutes. After washing with DMF (35 mL), a solution of D-biotin (5 eq.), HBTU (4.75 eq.) and .sup.iPr.sub.2NEt (10 eq.) in DMF (1 mL) was added to the resin, and the reaction mixture was agitated at room temperature for 30 minutes then washed with DMF (35 mL).

[0107] General Method K: Cleavage of Peptide from Resin

[0108] The resin containing the desired linear peptide was agitated in a mixture of TFA/H.sub.2O/DODT/TIPS (94:2.5:2.5:1.0, 5 mL, v/v/v/v) for 3 hours. To the filtrate was added cold diethyl ether (30 mL), and the product mixture was centrifuged for 10 minutes before the supernatant was discarded. This procedure was repeated two times. The resultant solid was dissolved in a solution of H.sub.2O/CH.sub.3CN+0.1% TFA (15 mL) and lyophilised.

[0109] General Method L: Purification

[0110] The crude peptide was dissolved in a solution of H.sub.2O/0.1% TFA and purified by preparative reverse-phase (RP)-HPLC on a XTerra C18 column using a gradient of 5-20% B at 0.5% B/min then 0.2% B/min up to 35% B, at a flow rate of 10 mL/min. The purity of the peptide was determined by flow injection (ESI.sup.+, 100V) and analytical RP-HPLC (XTerra C18 column, 5-95% B, 3% B/min, 1 mL/min).

[0111] Biology Studies

[0112] Preparation of Peptide

[0113] Note that for comparison commercially sourced biotinylated DOTA-A20FMDV2 peptide, (95% purity) was purchased from PPR (Cambridge, UK). The peptides were re-suspended in 0.1% TFA (diluted in water) to prepare 1 mM concentration of stock solutions which were aliquoted and stored at 20 C.

[0114] Cell Lines

[0115] The cell lines used in vitro and in vivo are the transduced melanoma lines A375Ppuro, and A375P6 (cultured in Dulbecco's Modified Eagle's Medium (DMEM)/10% fetal bovine serum (FBS) [9].

[0116] Specificity and Level of Binding of Peptides-Flow Cytometry Method

[0117] Cells were trypsinised and re-suspended into DMEM/0.1% (w/v) sodium azide/0.1% (w/v) BSA (flow media) to prepare a cell suspension of 410.sup.6 cells/ml. From this point on everything was kept on ice, 50 l of cell suspension was aliquoted into each flow tube (Falcon 2054-Millipore). Peptides were serially diluted in the flow media at 2 concentration therefore when 50 l of each concentration was added to the 50 l cells it gave the final concentrations of 1000 nM, 100 nM, 10 nM, 1 nM, 0.1 nM and 0 nM. For A375Ppuro cells, only the top concentration of 1000 nM was added to the cells. The peptides were then left on ice for 15 minutes. Cells were then washed twice by resuspension in flow media and centrifugation for 3 minutes at 1200 rpm.

[0118] Mouse anti-biotin (50 l at 1:200; Jackson ImmunoResearch, 200-002-211) was added to each sample for 15 minutes, then wash steps were repeated. Goat anti-mouse IgG conjugated to Alexa 488 (1:250) was added (50 l) to each sample and left for 15 minutes on ice in the dark. The wash step was repeated and the cells were resuspended in 380 l of flow media. FACSCalibur cytometer (Becton-Dickinson) was used to acquire the data; geometric mean fluorescence intensity was recorded for each sample.

[0119] Internalisation Assay MethodImagestream and Flow Cytometry

[0120] Cells were trypsinised and resuspended into DMEM (serum-free media) to prepare a cell suspension of 410.sup.6 cells/ml. From this point on everything was kept on ice. 50 l of cell suspension were aliquoted into each flow tube. Peptides were diluted in ice-cold serum-free media to 200 nM giving the final concentration of 100 nM when 50 l was added to the cell samples. The peptides were left on ice for 15 minutes then washed twice with flow media and centrifuged for 3 minutes at 1200 rpm in between each wash step. Mouse anti-biotin (50 l at 1:200) was added to each sample for 15 minutes, then wash steps were repeated. Apart from the 0 time point, each of the time point samples were put in the incubator at 37 C. and at 15, 30 and 45 minutes the cells were fixed in 4% formaldehyde in PBS for 10 minutes, washed once in PBS and 0.1% Triton X-100 detergent added for 5 minutes, before washing in PBS again. Goat anti-mouse IgG conjugated to AlexaFLUOR 488 (1:250) was added (50 l) to each sample and left for 15 minutes on ice in the dark. Samples were washed as above and resuspended to 30 l. Samples were examined on an Imagestream X Mark II (Amnis, Merck) Imagestream images were assessed for internalisation compared with the 0 minute samples using on board software.

[0121] Internalisation Assay MethodFlow Cytometry

[0122] Cells were prepared as above except that no detergent was added prior to detecting the biotin with antibodies. Samples were analysed on a FACScalibur (Bekton-Dickinson) cytometer. Reduction in fluorescence signal measured over time was associated with internalization of bound peptide as confirmed visually using the Imagestream (data not shown).

[0123] Plasma Stability

[0124] To 15 g DTPA-conjugated peptide 15 MBq of Indium-111 (CovidienPetten, Netherlands) was added (final volume 20 l) followed by 5 l Ammonium Acetate (1M). Samples were mixed and left for 30 minutes at room temperature. 2 l of this mixture was added to 100 l distilled water then the mixture injected into the gradient Reverse Phase-HPLC (Beckman). The sample was run through a Agilent Eclipse XDB-C18 Column in 0.1% TFA in distilled water. This was to check efficiency of radiolabelling which was typically >95%. Human blood was taken in sodium heparin tubes and centrifuged at 2000 g for 10 mins. Plasma (300 l) was incubated with 7.5MBq of variant peptide and immediately 150 l was removed and placed at 37 C. and the other 150 l was used as the time 0 minutes sample. To this was added and an equal volume of ice-cold Acetonitrile (1:1) and samples were mixed and centrifuged at 14000 rpm for 5 minutes. The supernatants were collected and vacuumed dried for 10 mins to remove acetonitrile. The residuum was filtered through a 0.22 m filter (to remove particulates) and 100 l was injected into the Radio-HPLC machine. The 24 h samples were processed similarly. Control samples were incubated with PBS. (Note: PBS control did not require this process of filtration or addition of acetonitrile). Samples were performed in duplicate with similar results.

[0125] Biodistribution

[0126] 210.sup.6 cells in 100 l were injected subcutaneously into the shoulders of female CD1 Nu/Nu mice. Tumours were grown subcutaneously on the left (A375Puro) and on the right (A375136) shoulder over two weeks. Once tumours had grown to approximately 5 mm diameter peptides were radiolabelled with Indium-111, and analysed by Radio-HPLC to determine labelling efficiency. The labelled peptides were diluted in sterile PBS/BSA and were dosed to give 0.3MBq per animal. Mice were then intravenously (tail-vein) injected with the radiolabelled peptide and are culled after 1 hour. Blood, organs and tumours were removed, weighed and residual activity was measured on a gamma counter (LKB Compugamma) the next day. Data were expressed as % Injected Dose/g tissue (% ID/g).

[0127] Peptide Characterisation Data

TABLE-US-00003 Peptide (SEQIDNO:11) H.sub.2N-NK(Biotin)VPNLRGDLQVLAQKVART-OH(1)

[0128] Peptide (1) (97.1 mg, 50%) was obtained as a white solid in >99% purity according to analytical RP-HPLC. R.sub.t=13.2 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1224.3; Found 1223.6.

TABLE-US-00004 Peptide (SEQIDNO:12) H.sub.2N-NK(Biotin)VPNLRGDLQVLAQkVART-OH(2)

[0129] Peptide (2) (54.3 mg, 22%) was obtained as a white solid in >99% purity according to analytical RP-HPLC. R.sub.t=11.9 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1224.3; Found 1223.7.

TABLE-US-00005 Peptide (SEQIDNO:13) H.sub.2N-NK(Biotin)VPNLRGDLQVLAQ[ornithine]VART-OH(3)

[0130] Peptide (3) (63.5 mg, 26%) was obtained as a white solid in >99% purity according to analytical RP-HPLC. R.sub.t=12.7 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1217.3; Found 1216.7.

TABLE-US-00006 Peptide (SEQIDNO:14) N-NK(Biotin)VPNLRGDLQVLAQ[diaminobutyricacid] VART-OH(4)

[0131] Peptide (4) (70.3 mg, 29%) was obtained as a white solid in >99% purity according to analytical RP-HPLC. R.sub.t=12.7 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1210.3; Found 1209.8.

TABLE-US-00007 Peptide (SEQIDNO:15) H.sub.2N-NK(Biotin)VPNLRGDLQVLAQ[diaminopropionicacid] VART-OH(5)

[0132] Peptide (5) (59.9 mg, 25%) was obtained as a white solid in >99% purity according to analytical RP-HPLC. R.sub.t=12.9 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1203.2; Found 1203.1.

TABLE-US-00008 Peptide (SEQIDNO:16) H.sub.2N-NK(Biotin)VPNLRGDLQVLAQ-N-MeKVART-OH(6)

[0133] Peptide (6) (72.7 mg, 30%) was obtained as a white solid in >99% purity according to analytical RP-HPLC. R.sub.t=11.5 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1231.3; Found 1230.7.

TABLE-US-00009 Peptide (SEQIDNO:17) H.sub.2N-NK(Biotin)VPNLRGDLQV[aminoisobutyricacid] AQKVART-OH(7)

[0134] Peptide (7) (16.6 mg, 7%) was obtained as a white solid in >99% purity according to analytical RP-HPLC. R.sub.t=11.9 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1209.7; Found 1210.2.

TABLE-US-00010 Peptide (SEQIDNO:18) H.sub.2N-NK(Biotin)VPNLRGDLQV[norvaline]AQKVART-OH (8)

[0135] Peptide (8) (19.5 mg, 8%) was obtained as a white solid in >99% purity according to analytical RP-HPLC. R.sub.t=12.2 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1216.8; Found 1217.2.

TABLE-US-00011 Peptide (SEQIDNO:19) H.sub.2N-NK(Biotin)VPNLRGDLQV[norleucine]AQKVART-OH(9)

[0136] Peptide (9) (18.7 mg, 8%) was obtained as a white solid in >99% purity according to analytical RP-HPLC. R.sub.t=12.7 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1223.8; Found 1224.7.

TABLE-US-00012 Peptide (SEQIDNO:20) H.sub.2N-NK(Biotin)VPNLRGDLQV[allylglycine] AQKVART-OH(10)

[0137] Peptide (10) (5.5 mg, 2%) was obtained as a white solid in >99% purity according to analytical RP-HPLC. R.sub.t=11.7 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1215.7; Found 1215.8.

TABLE-US-00013 Peptide (SEQIDNO:21) H.sub.2N-NK(Biotin)VPNLRGDLQV[tert-butyl-alanine] AQKVART-OH(11)

[0138] Peptide (11) (7.5 mg, 3%) was obtained as a white solid in >99% purity according to analytical RP-HPLC. R.sub.t=12.9 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1230.8; Found 1230.7.

TABLE-US-00014 Peptide (SEQIDNO:22) H.sub.2N-NK(Biotin)VPNLRGDLQV[homoleucine]AQKVART-OH (12)

[0139] Peptide (12) (26.1 mg, 11%) was obtained as a white solid in >99% purity according to analytical RP-HPLC. R.sub.t=13.1 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1230.8; Found 1231.2.

TABLE-US-00015 Peptide (SEQIDNO:23) H.sub.2N-NK(Biotin)VPNLRGDLQV[2-amino-3-ethylpentanoic acid]AQKVART-OH(13)

[0140] Peptide (13) (10.1 mg, 4%) was obtained as a white solid in >99% purity according to analytical RP-HPLC. R.sub.t=12.9 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1230.8; Found 1230.8.

TABLE-US-00016 Peptide (SEQIDNO:24) H.sub.2N-NK(Biotin)VPNLRGDLQV[cyclohexylalanine]AQKVART- OH(14)

[0141] Peptide (14) (6.2 mg, 2%) was obtained as a white solid in >99% purity according to analytical RP-HPLC. R.sub.t=13.4 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1243.8; Found 1244.2.

TABLE-US-00017 Peptide (SEQIDNO:25) H.sub.2N-NK(Biotin)VPNLRGDLQV[adamantylglycine]AQKVART- OH(15)

[0142] Peptide (15) (22.4 mg, 9%) was obtained as a white solid in >99% purity according to analytical RP-HPLC. R.sub.t=13.7 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1262.8; Found 1263.3.

TABLE-US-00018 Peptide(16) (SEQIDNO:11) PeptideAcHN-NK(Biotin)VPNLRGDLQVLAQKVART-OH(16)

[0143] (with N-term. acetylation) (30.1 mg, 12%) was obtained as a white solid in >99% purity according to analytical RP-HPLC. R.sub.t=13.9 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1244.8; Found 1245.2.

TABLE-US-00019 Peptide (SEQIDNO:11) H.sub.2N-NK(Biotin)VPNLRGDLQVLAQKVART-NH.sub.2(17)

[0144] (with C-term. amidation)

[0145] Peptide (17) (13.4 mg, 5%) was obtained as a white solid in >95% purity according to analytical RP-HPLC. R.sub.t=13.5 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1223.8; Found 1223.3.

TABLE-US-00020 Peptide(18) (SEQIDNO:11) PeptideAcHN-NK(Biotin)VPNLRGDLQVLAQKVART-NH.sub.2(18)

[0146] (with N-term. acetylation and C-term. amidation) (12.5 mg, 5%) was obtained as a white solid in >95% purity according to analytical RP-HPLC. R.sub.t=13.9 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1244.3; Found 1244.6.

TABLE-US-00021 Peptide (SEQIDNO:8) H.sub.2N-nK(Biotin)VPNLRGDLQVLAQKVART-OH(19)

[0147] Peptide (19) (47.7 mg, 19%) was obtained as a white solid in >95% purity according to analytical RP-HPLC. R.sub.t=12.6 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1223.8; Found 1224.1.

TABLE-US-00022 Peptide (SEQIDNO:26) H.sub.2N-NK(Biotin)VPNLRGDLQVLAQKVARt-OH(20)

[0148] Peptide (20) (45.3 mg, 19%) was obtained as a white solid in >95% purity according to analytical RP-HPLC. R.sub.t=13.0 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1223.8; Found 1224.2.

TABLE-US-00023 Peptide (SEQIDNO:9) H.sub.2N-nK(Biotin)VPNLRGDLQVLAQKVARt-OH(21)

[0149] Peptide (21) (36.4 mg, 15%) was obtained as a white solid in >95% purity according to analytical RP-HPLC. R.sub.t=12.9 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1223.8; Found 1224.4.

TABLE-US-00024 Peptide (SEQIDNO:11) DTPA-NK(Biotin)VPNLRGDLQVLAQKVART-OH(22) (N-term.DTPA)

[0150] Peptide (22) (53.7 mg, 24%) was obtained as a white solid in >99% purity according to analytical RP-HPLC. R.sub.t=13.3 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1411.9; Found 1411.6.

TABLE-US-00025 Peptide (SEQIDNO:8) DTPA-nK(Biotin)VPNLRGDLQVLAQKVART-OH(25) (N-term.DTPA)

[0151] Peptide (25) (37.5 mg, 13%) was obtained as a white solid in >95% purity according to analytical RP-HPLC. R.sub.t=12.6 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1411.3; Found 1410.6.

TABLE-US-00026 Peptide (SEQIDNO:9) DTPA-nK(Biotin)VPNLRGDLQVLAQKVARt-OH(26) (N-term.DTPA)

[0152] Peptide (26) (12.5 mg, 4%) was obtained as a white solid in >95% purity according to analytical RP-HPLC. R.sub.t=12.9 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1411.3; Found 1410.6.

TABLE-US-00027 Peptide (SEQIDNO:11) DTPA-NK(Biotin)VPNLRGDLQVLAQKVART-NH.sub.2(24) (N-term.DTPAandC-term.amidation)

[0153] Peptide (24) (12.1 mg, 4%) was obtained as a white solid in >95% purity according to analytical RP-HPLC. R.sub.t=13.0 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1410.8; Found 1410.1.

TABLE-US-00028 Peptide (SEQIDNO:27) DTPA-GNK(Biotin)VPNLRGDLQVLAQKVART-OH(23) (N-term.DTPA)

[0154] Peptide (23) (41.9 mg, 15%) was obtained as a white solid in >95% purity according to analytical RP-HPLC. R.sub.t=12.6 min (XTerra C18, 5-95% B, 3% B/min, 1.0 mL/min); m/z (ESI-MS): [M+2H].sup.2+ Calc. 1439.9; Found 1439.2.

Example 1Synthesis of Biotinylated A20FMDV2 1, Lys16 or Leu13-Modified and Biotinylated Peptides 2-15, N- and/or C-Terminus-Modified and Biotinylated Peptides 16-21 and (DTPA)-Containing Peptides 22-26

[0155] To enable investigation of introducing non-proteinogenic amino acids (listed in FIG. 1) on A20FMDV2 binding activity, biotinylated peptides 1-15 (see Table 1), except for peptide 6, were synthesised by standard Fmoc SPPS on the acid liable hydroxymethylphenoxypropionic acid linker (HMPP) which delivers a C-terminal carboxylic acid using to the conditions depicted in Scheme 1. The desired peptide sequences were assembled using 20% piperidine/DMF to remove the Fmoc protecting group and 0-(benzotriazol-1-yl)-N,N,N,N-tetramethyluronium hexafluorophosphate (HBTU)/DIPEA as coupling reagents.

[0156] Since specific binding to the v6 integrin was to be studied by flow cytometry, the native alanine at the second residue in A20FMDV2 (1) and all analogues thereof, were substituted with a biotinylated lysine residue. This substitution has previously been shown to be well tolerated [24,25]. We chose to install the D-biotin moiety by selective deprotection of a 1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl (Dde) [19] group on the side chain Ns-amino group followed by condensation with D-biotin using HBTU/DIPEA. Trifluoroacetic acid (TFA)/H.sub.2O/3, 6-dioxa-1, 8-octanedithiol (DODT)/triisopropylsilane (TIPS) (94:2.5:2.5:1.0, v/v/v/v) effected cleavage of the synthesised peptides from the corresponding peptidyl-resins. Peptides 1-15 were obtained in good yields ranging from 2%-50% and purity exceeding 99% (see peptide characterization data).

[0157] For the synthesis of peptide 6 containing an N-L-methyllysine modification we employed an on-resin N-methylation protocol [22] which furnished peptide 6 in good yield (30%) following TFA-mediated peptide cleavage and RP-HPLC purification.

[0158] The lead peptide, A20FMDV2, which contains all naturally-occurring amino acids would be susceptible to degradation by exopeptidases which act on the amino- and carboxy terminuses. To mitigate this, six N- and/or C-terminus-modified and biotinylated A20FDMV2 mimics were prepared wherein we systematically modified the amino and carboxy ends (peptides 16-18) and the N-terminal and C-terminal amino acids (Asn1 and Thr20, respectively, peptides 19-21). N-terminal/C-terminal modified peptides 16-18 were obtained by capping of the N-terminus with acetic anhydride (16) or by employing the Rink amide linker to afford the C-terminal carboxamide (17) or a combination of both (peptide 18).

[0159] Peptide 19, bearing the unnatural D-Asn1 in place of the native Asn1 at the N-terminus of biotinylated A20FMDV2 (1) was obtained using the synthetic route outlined in Scheme 1 except that the Fmoc-D-Asn(Trt)-OH building block was incorporated into the synthesis as the N-terminal residue. For the preparation of peptides 20 and 21, which contains the unnatural D-Thr at the C-terminus, HMP-anchored resin 27 (see Scheme 1, HMP=hydroxymethylphenoxyacetic acid) was first esterified with Fmoc-D-Thr(.sup.tBu)-OH using DIC/DMAP and the sequence then elongated by Fmoc SPPS.

TABLE-US-00029 TABLE 1 List of prepared synthetic peptides [N-term]-X.sub.1K(Biotin)VPNLRGDLQVX.sub.2AQX.sub.3VARX.sub.4-[C-term] containing substitutions for the native Lys16 (peptides 2-6) or Leu13 (peptides 7-15), C-terminal/N-terminal variants (peptides 16-21) and DTPA-modified peptides (22-26). NB: nomenclature, particularly X position numbering used in this table is not the same as that used in the claims. Com- N- C- pound term. X.sub.1 X.sub.2 X.sub.3 X.sub.4 term. 1 NH.sub.2 Asn Leu Lys Thr CO.sub.2H 2 NH.sub.2 Asn Leu D-Lys Thr CO.sub.2H 3 NH.sub.2 Asn Leu L-Orn Thr CO.sub.2H 4 NH.sub.2 Asn Leu 1-2,4- Thr CO.sub.2H diamino- butyric acid 5 NH.sub.2 Asn Leu 1-2,3- Thr CO.sub.2H diamino- propionic acid 6 NH.sub.2 Asn Leu N-L- Thr CO.sub.2H methyl- lysine 7 NH.sub.2 Asn L-2- Lys Thr CO.sub.2H aminoiso- butyric acid 8 NH.sub.2 Asn L-norvaline Lys Thr CO.sub.2H 9 NH.sub.2 Asn L-norleucine Lys Thr CO.sub.2H 10 NH.sub.2 Asn L-allylglycine Lys Thr CO.sub.2H 11 NH.sub.2 Asn L-tert- Lys Thr CO.sub.2H butylalanine 12 NH.sub.2 Asn L-homoleucine Lys Thr CO.sub.2H 13 NH.sub.2 Asn L-2-amino-3- Lys Thr CO.sub.2H ethylpentanoic acid 14 NH.sub.2 Asn L- Lys Thr CO.sub.2H cyclohexyl- alanine 15 NH.sub.2 Asn L- Lys Thr CO.sub.2H adamantyl- glycine 16 AcNH Asn Leu Lys Thr CO.sub.2H 17 NH.sub.2 Asn Leu Lys Thr CONH.sub.2 18 AcNH Asn Leu Lys Thr CONH.sub.2 19 NH.sub.2 D- Leu Lys Thr CO.sub.2H Asn 20 NH.sub.2 Asn Leu Lys D- CO.sub.2H Thr 21 NH.sub.2 D- Leu Lys D- CO.sub.2H Asn Thr 22 DTPA- Asn Leu Lys Thr CO.sub.2H NH 23 DTPA- Asn Leu Lys Thr CO.sub.2H Gly-NH 24 DTPA- Asn Leu Lys Thr CONH.sub.2 NH 25 DTPA- D- Leu Lys Thr CO.sub.2H NH Asn 26 DTPA- D- Leu Lys D- CO.sub.2H NH Asn Thr

##STR00001## ##STR00002##

[0160] The results obtained from the binding assays (Table 2, see later) showed that modification of the N- and C-terminus of 1 (peptides 16 and 17 respectively) or substitution of the native Asn1, and both Asn1 and Thr20 residues of A20FMDV2 (1) for their D-counterparts (peptides 19 and 21, respectively) resulted in peptides that exhibited improved biological activity compared to 1. Four N- and C-termini-modified analogues thereof (16, 18, 19 and 21) were therefore selected for incorporation of the DTPA chelating agent to enable cell internalisation studies and degradation assays in human plasma to be carried out. The DTPA-containing, biotinylated A20FMDV2 peptide (22) was also prepared as a control [25].

[0161] As depicted in Scheme 1, the DTPA-containing, biotinylated A20FMDV2 peptide 22 and analogues 23-25) were synthesised using Fmoc SPPS conditions (20% piperidine/DMF for Fmoc protecting group removal and HBTU/DIPEA as coupling reagent). To attach DTPA at the N-terminus of A20FMDV2 and D-biotin at the side chain of Lys2, the N-terminal Fmoc protecting group was first removed using 20% piperidine/DMF, and tert-butyl protected DTPA [21] was coupled to the resultant N-amino group using HBTU/DIPEA. As the four carboxylic acids of DTPA were protected as acid-labile tert-butyl esters, the Dde protecting group could be selectively removed using 2% hydrazine/DMF and D-biotin coupled to the side chain amino lysyl using HBTU/DIPEA. In the case of peptides 23 and 24 to enable the incorporation of the DTPA ligand a glycine spacer was employed to mimic the acetyl group of peptides 16 and 18 and to allow facile attachment of DTPA via amide bond formation.

Example 2Biological Activity of Peptide Variants

[0162] To test which, if any, of the peptide variants is superior to the original A20FMDV2 we designed a series of tests using two cell lines (A375Ppuro and A37546) that were genetically identical except for the expression of integrin v6 in the A37546 cell lines [9]. Since A375Ppuro expresses four integrins (v3, v5, v8 and 51) that also bind to RGD motifs in their ligands, comparing binding activity on these two cell lines is considered a highly stringent assay.

[0163] As an example of the assays used for characterizing the behaviour of modified peptides 1-15, 16-21 and 22-25, FIG. 2 shows a comparison between peptides 22 and 25. A20FMDV2 binds to v6>1000-times more selectively than to other integrins [9]. To confirm that modified peptides retained specificity we determined how much peptide bound to A375Ppuro versus A37546 cells using flow cytometry. FIG. 2A shows that at 1000 nM neither peptide 22 (Ai) nor peptide 25 (Aii) bound to A375Ppuro (red histograms; upper panels). In contrast both peptides bound well to A37546 (blue histograms; lower panels) at 100 nM. These data show that v6 binding specificity is retained in these peptide variants. Moreover, every peptide variant failed to bind to A375Ppuro at 1000 nM (data not shown) showing that all peptides retained specificity.

[0164] To determine whether the modified peptides bound as well or better than the parent biotinylated-A20FMDV2 peptide at 100 nM we tested binding activity of variants at 0, 0.1, 1, 10, 100 and 1000 nM to A37546.

[0165] As an example, FIG. 2B shows that peptide 22, is better than the commercially obtained biotinylated-A20FMDV2 as it binds 16% higher at 100 nM. Similarly, peptide 25 is even better since at 100 nM binding is at 150% the commercially obtained biotinylated-A20FMDV2. These data were from single experiments. Table 2 shows the mean of up to four experiments for all peptides studied and shows overall, peptide 22 had on average 5% higher activity than the parent (i.e. commercially obtained biotinylated-A20FMDV2) and peptide 25 was 36% higher than the parent.

[0166] To assess ability to be internalized by cells at 37 C. (and thus potential vectors for therapies) we used Imagestream cytometry and flow cytometry. Imagestream takes a fluorescence image of each cell (FIG. 2C) enabling image analysis of the fluorescence on the surface versus the intracellular compartment. Histograms in FIG. 2C plot internalization relative to the 0 minute time point. For flow cytometry we monitored the loss of surface expression as the peptides were internalized.

[0167] Table 2 summarizes the activity and internalization data for all peptides used in this study relative to the commercially sourced biotinylated-A20FMDV2 (the biotinylated A20FMDV2 (1), synthesized in this study, differs from the commercially obtained biotinylated-A20FMDV2 in that peptide (1) comprises the Ala2Lys mutation utilized to couple D-biotin).

[0168] Table 2 also provides an arbitrary value for each peptide's potential for intracellular drug delivery by multiplying binding affinity value by the amount internalized to give a Relative Activity value. It can be seen that most .sup.16Lys and .sup.13Leu modifications reduced relative activity; with the exception of peptides (7) and (9) their Relative Activity was lower than control biotinylated-A20FMDV2. In contrast most of the N- and C-terminus modified peptides (16-19 and 21) had better binding affinity and had improved Relative Activity compared to biotinylated-A20FMDV2 (1). For example, peptide 19 that has a non-proteinogenic D-Asn amino acid N-terminus modification bound on average 43% better to cellular v6 than the parent compound (Table 2). Relative to unmodified, A20FMDV which has a value of 1.0 peptides 16 (N-acetylated), 17 (C-amidated), 18 (N-acetylated and C-amidated), 19 (D-Asn substitution) and 21 (both D-Asn and D-Thr substitution), have Relative Activity values of 55%, 31%, 9%, 27%, and 37% higher than the control peptide 1.

TABLE-US-00030 TABLE 2 Comparison of internalization data for Lys16 (1-6) or Leu13 (7-15) or C- or N-terminal modified (16-21) and DTPA-coupled (22-26).sup.a synthetic peptides. A) B) Relative Compound Affinity.sup.b Internalisation.sup.c Activity (A B) A20FMDV2.sup.d 1.00 1.00 1.00 1.sup.e 1.11 0.15 0.84 0.14 0.93 2 1.11 0.15 0.78 0.15 0.87 3 1.12 0.16 0.86 0.29 0.96 4 1.00 0.07 0.86 0.29 0.86 5 0.79 0.14 0.96 0.31 0.76 6 0.37 0.12 0.89 0.32 0.32 7 1.07 0.37 1.11 0.3 1.19 8 0.77 0.52 1.09 0.17 0.84 9 1.16 0.29 1.15 0.04 1.33 10 0.58 0.25 0.82 0.25 0.48 11 0.60 0.23 1.03 0.14 0.62 12 0.45 0.22 0.66 0.14 0.27 13 0.70 0.33 0.52 0.23 0.37 14 0.62 0.06 1.01 0.32 0.62 15 0.51 0.28 1.07 0.18 0.55 16 1.48 0.49 1.05 0.24 1.55 17 1.23 0.25 1.07 0.40 1.31 18 1.25 0.26 0.87 0.12 1.09 19 1.43 0.51 0.89 0.12 1.27 20 0.53 0.44 0.99 0.25 0.53 21 1.57 0.55 0.87 0.27 1.37 22 1.01 0.21 1.05 0.07 1.06 23 1.28 0.23 0.97 0.11 1.24 24 1.19 0.30 0.98 0.12 1.17 25 1.36 0.42 0.99 0.10 1.34 26 1.19 0.40 1.04 0.16 1.24 .sup.aSpecific peptides (1, 16, 17, 19, 21) were DTPA-coupled. .sup.bMean activity relative to biotinylated A20FMDV2 (100 nM). .sup.cMean % internalisation at 45 min relative to biotinylated A20FMDV2 (100 nM) using flow cytometry. .sup.dBiotinylated DOTA-A20FMDV2 obtained commercially. .sup.eBiotinylated A20FMDV2 synthesised in this work.

[0169] Encouragingly, conjugation of DTPA to lead peptides (16, 17, 19, 21) to create peptides 23-26, respectively, had very little effect on binding affinity or internalization and thus maintained their increased Relative Activity.

Example 3Plasma Stability and Bio-Distribution Studies

[0170] FIG. 3 shows the stability of DTPA-conjugated peptides (22-26) in plasma (red bars; right-hand bar for each peptide) versus PBS (black bars; left-hand bar for each peptide) at 37 C., relative to a 0 minutes time point. The data show that after 24 h at 37 C. in PBS only about 10% of the peptide has degraded. In contrast, while peptides (22, 25, 26) show similar levels (77%-80%) remaining in plasma after 24 hours, there is major degradation of peptide (23) (60% remaining) and peptide (24) (52% remaining). Thus, the modifications of peptides 24 and 23 (C-terminal amidation and N-terminal acetylation, respectively) have increased susceptibility to plasma degradation relative to the control parent peptide (1). Peptide modification by chemical manipulation using D amino acids (D-Asn, compound 25, and D-Asn/D-Thr compound 26) was optimal in improving susceptibility to human plasma proteases.

[0171] Immunocompromised mice (n=3-5) bearing A375Ppuro and A37546 tumours on opposite shoulders were given intravenous (iv) injections of 300 Bq of radiolabelled peptides 22-26 then killed 1 h later. Major organs and blood were collected immediately, weighed, and radioactivity determined. The data in Table 3 show the behaviour of the five DTPA-conjugated peptides tested; data are expressed as mean % injected dose/g tissue.

TABLE-US-00031 TABLE 3 Bio-distribution (Mean (%) ID/g SEM) data for .sup.111In-DTPA labelled-peptides (22-26) Tissue 22 23 24 25 26 Tumour (v6) .sup.a 3.1 0.18 3.7 0.29 3.8 0.31 4.8 2.43 3.4 0.21 Tumour 0.5 0.04 0.5 0.15 0.4 0.04 0.5 0.11 0.5 0.24 (Control) .sup.a Intestines 4.1 0.23 3.8 0.98 3.4 0.29 4.2 0.06 3.9 0.22 Pancreas 0.5 0.06 0.5 0.13 0.5 0.03 0.5 0.03 0.5 0.03 Spleen 0.1 0.01 0.2 0.07 0.2 0.01z 0.1 0.01 0.19 0.01 Stomach 6.5 1.05 6.4 2.33 4.6 0.63 6.4 0.97 6.6 0.71 Kidney 85.9 8 154.0 19.44 131.2 12 67.0 6.65 62.0 3.98 Liver 0.3 0.02 0.4 0.06 0.3 0.05 0.3 0.03 0.4 0.03 Heart 0.6 0.06 0.6 0.16 0.66 0.02 0.7 0.01 0.7 0.07 Lung 2.7 0.24 4.4 0.72 3.62 0.30 2.2 0.22 2.5 0.17 Blood 0.4 0.03 0.5 0.16 0.3 0.04 0.4 0.05 0.5 0.01 Muscle 1.1 0.10 0.8 0.07 1.1 0.05 0.9 0.09 1.2 0.1 Tail 2.1 0.43 4.3 2.85 1.0 0.19 0.8 0.04 1.3 0.39 .sup.a Data are derived from excised tissues taken from mice (n = 3) bearing pairs of A375136 (v6) and A375Puro (control) xenografts. Mice were culled 1 h after iv injection of 100 Bq of individual peptides. Data are displayed as mean % injected dose per gram of tissue standard error of the mean. Bq: Becquerel.

[0172] As with our previous studies, there is significant retention in the gastrointestinal tract (stomach and intestines) and also the lungs [9, 24]. The kidney retention, which we reported is independent of v6 [9], is highly varied for the five peptides with peptides 25 and 26 showing the least retention and peptides 23 and 24 showing retention far greater than peptide 22, which is the parent biotinylated-A20FMDV2. There is a robust selective uptake of each peptide by the v6-positive tumour compared with the v6-negative control tumour. FIG. 4 highlights these differences in a histogram. While there is no statistical increased uptake of the peptides 23-26 versus the DTPA-labelled parent peptide 22, all the variants have slightly higher mean ratio of retention in the v6-positive tumour verses v6-negative tumour compared to the control peptide 22. The highest ratio of retention in the v6-positive tumour verses v6-negative tumour compared to the control peptide 22 was seen with peptide 25.

[0173] Discussion

[0174] The 20-residue linear peptide A20FMDV2 exhibits high specificity and affinity for the tumour-related v6 integrin, and also exhibits v6-dependent internalisation into cells. A20FMDV2 is therefore considered a promising lead compound to deliver therapeutic loads (e.g. chemotherapeutic payloads) to v6-expressing cancer cells. In the Examples above, the impacts of non-proteinogenic substitutes of the native amino acid residues of A20FMDV2 on in vitro behaviour, plasma stability and in vivo bio-distribution have been investigated.

[0175] All of the peptides described herein were synthesised in good yield and excellent purity by Fmoc SPPS. Binding studies to the v6 integrin showed that all the A20FMDV2 analogues bound only to A375P6 cells but not A375Ppuro cells showing that specificity had not been affected by modifications. Moreover, peptides incorporating an acetylated N-terminus and an amidated C-terminus or the unnatural D-version of the native .sup.1Asn and .sup.20Thr residues exhibited more potent v6-binding activity than the parent peptide (A20FMDV2) and also were more potent than most peptides containing non-proteinogenic substitutes of the native .sup.16Lys and .sup.13Leu residues. For example, peptide 19 that has a non-proteinogenic D-Asn amino acid N-terminus modification bound on average 43% better to cellular v6 than the parent compound (Table 2).

[0176] We have assessed stability in human blood plasma and showed that the peptides remained intact for much longer than in our previous studies in mouse serum which suggests that human plasma is less degradative than mouse serum for these peptides. While over 90% of all radiolabelled peptides remained intact in PBS after 24 h at 37 C., only A20FMDV2 containing D amino acids 25 and 26 remained mostly intact (76-80%) after 24 h in human plasma at 37 C.

[0177] The modifications had only moderate effects on the degree of internalisation into v6-expressing cells. Thus, Table 2 shows that for all peptides tested, internalisation varied from 0.78 to 1.11 fold relative to commercial biotinylated-A20FMDV2. Since both the binding affinity and internalisation of the peptide is necessary to consider for delivery of an intracellular cytotoxic, Table 2 also shows an arbitrary value for each peptide's Relative Activity. The control peptide has a value of 1.0 whereas peptides 16, 19, 17, 18, and 21, have Relative Activity values of 55%, 27%, 31%, 9% and 37% higher than the control peptide, respectively.

[0178] For v6-targeting peptides to deliver therapies they must be selectively retained in v6-expressing tumours. In bio-distribution studies we found that all of the five lead peptides tested (22-26) were selectively retained in the v6-positive tumours at least six- to ten-fold higher levels than the v6-negative tumours. It is encouraging that all the modified peptides were slightly better than the DTPA-labelled and biotinylated peptide 22. The present results show that chemical modification of A20FMDV2 has improved its capacity for selectively locating to v6-expressing cancers.

REFERENCES

[0179] A number of publications are cited above in order to more fully describe and disclose the invention and the state of the art to which the invention pertains. Full citations for these references are provided below. The entirety of each of these references is incorporated herein. [0180] [1] DiCara et al., J. Biol. Chem., 2007, Vol. 282, pp. 9657-9665. [0181] [2] Jackson et al., J. Virol., 2000, Vol. 74, pp. 4949-4956. [0182] [3] Logan et al., Nature, 1993, Vol. 362, pp. 566-568. [0183] [4] Bandyopadhyay et al., Curr. Drug Targets, 2009, Vol. 10, pp. 645-652. [0184] [5] Hazelbag et al., J. Pathol., 2007, Vol. 212, pp. 316-324. [0185] [6] Elayadi et al., J. Cancer Res., 2007, Vol 67, pp. 5889-5895. [0186] [7] Thomas et al., J. Oral Pathol. & Med., 2006, Vol. 35, pp. 1-10. [0187] [8] Bates et al., J. Clin. Invest., 2005, Vol. 115, pp. 339-347. [0188] [9] Saha et al., J. Pathol., 2010, Vol. 222, pp. 52-63. [0189] [10] DiCara et al., J. Virol., 2008, Vol. 82, pp. 1537-1546. [0190] [11] Munger et al., Cell, 1999, Vol. 96, pp. 319-328. [0191] [12] Firer et al., J. Heamatol. Oncol., 2012, Vol. 5, p. 70. [0192] [13] Hausner et al., Cancer Res., 2009, Vol. 69, pp. 5843-5850. [0193] [14] Gentilucci et al., Curr. Pharm. Des., 2010, Vol. 16, pp. 3185-3203. [0194] [15] Galati et al., Naturforsch. Sect. C J. Biosci. 2003, Vol. 58, pp. 558-561. [0195] [16] PeptideCutter. ExPASy Bioinformatics Resource Portal. Obtained from http://web.expasy.org/peptide_cutter/ [0196] [17] Safavy et al., J. Bioconjugate Chem., 2002, Vol. 13, pp. 317-326. [0197] [18] Nash et al., Tetrahedron Lett., 1996, Vol. 37, pp. 2625-2628. [0198] [19] Chatterjee et al., Nature Protoc., 2012, Vol. 7, pp. 432-444. [0199] [20] Harris et al., Synthesis, 2009, Vol. 20, pp. 3460-3466. [0200] [21] Arano et al., J. Med. Chem., 1996, Vol. 39, pp. 3451-3460. [0201] [22] Harris et al., Tetrahedron Lett., 2011, Vol. 52, pp. 6024-6026. [0202] [23] Hynes et al., Cell, 2002, Vol. 110, pp. 673-687. [0203] [24] John et al., J. Nucl. Med., 2013, Vol. 54, pp. 2146-2152. [0204] [25] Clinical Trial NCT02612051 https://clinicaltrials.gov/ct2/show/NCT02612051 (last accessed 31 Jan. 2017). [0205] [27] Ruoslahti et al., Annu. Rev. Cell Dev. Biol. 1996, Vol. 12, pp. 697-715. [0206] [28] Zhang et al., Viruses, 2013, Vol. 5, pp. 1114-1130. [0207] [29] Zhu et al., Mol. Pharmacueticals, 2014, Vol. 11, pp. 2108-1217. [0208] [30] Maltsev et al. Angew. Chem. Int. Ed., 2016, Vol. 55, pp. 1535-1539. [0209] [31] Liu et al., Am. J. Med. Mol. Imaging, 2014, Vol. 4, pp. 333-345. [0210] [32] Hausner et al., Cancer Res., 2007, Vol 67, pp. 7833-7840. [0211] [33] Hausner et al., J. Med. Chem., 2008, Vol. 51, pp. 5901-5904. [0212] [34] Hausner et al., Nucl. Med. Biol., 2013, Vol. 40, pp. 233-239. [0213] [35] Hausner et al., Mol. Imaging, 2009, Vol. 8, pp. 111-121. [0214] [36] Hu et al., Mol. Imaging Biol., 2014, Vol. 16, pp. 567-577. [0215] [37] Satpati et al., J. Radioanal. Nucl. Chem., 2014, Vol. 302, pp. 765-771. [0216] [38] Hamley, I. W., Biomacromolecules, 2014, Vol. 15, 1543-1559. [0217] [39] Hausner et al., J. Nucl. Med., 2015, Vol. 56, pp. 784-790. [0218] [40] Demmer et al., Design of cyclic peptides. In Peptide and protein design for biopharmaceutical applications, Jensen, K. J., Ed. John Wiley & Sons Ltd: 2009; pp 133-166. [0219] [41] Kaiser et al., Anal. Biochem. 1970, Vol. 34, pp. 595-598.

[0220] All references cited herein are incorporated herein by reference in their entirety and for all purposes to the same extent as if each individual publication or patent or patent application was specifically and individually indicated to be incorporated by reference in its entirety.

[0221] The specific embodiments described herein are offered by way of example, not by way of limitation. Any sub-titles herein are included for convenience only, and are not to be construed as limiting the disclosure in any way.