THERAPEUTIC PROTEINS FOR TREATING CANCERS AND METHODS FOR USING SUCH PROTEINS

Abstract

Therapeutic proteins for inducing apoptosis in cells and method for using such proteins are described. The protein, e.g., a chimeric protein, has a host peptide fused to a more stable BH3 domain peptide. The host peptide may be Calbindin D9k, a N-terminal or C-terminal half-domain of Calmodulin, Parvalbimin (“Pa”), an amino acid sequence variant thereof, or a modified variant thereof. The BH3 domain may be Bim, Bid, Bad, Bik, Bmf, Hrk, Puma, or Noxia. Moreover, various conjugates may be attached to the chimeric protein, including a folate and polyethylene glycol.

Claims

1. A chimeric protein capable of inducing apoptosis in cells, comprising: a first peptide is a host protein; and a second peptide is a BH3 domain of a BH3-only protein, the BH3 domain being from one of BH3-only proteins Bim, Bid, Bad, Bik, Bmf, Hrk, Puma, or Noxia.

2. The chimeric protein of claim 1, wherein the chimeric protein has an amino acid sequence selected from the group consisting of Sequence Id No. 1, Sequence Id. No. 2, Sequence Id. No. 3, Sequence Id. No. 4, Sequence Id. No. 5, Sequence Id. No. 6, Sequence Id. No. 7, Sequence Id. No. 8, Sequence Id. No. 9, and Sequence Id. No. 10.

3. The chimeric protein of claim 1, wherein the first peptide is selected from the group consisting of part of Calbindin D9k, N-terminal Calmodulin, C-terminal Calmodulin, and Parvalbimin.

4. The chimeric protein of claim 1, further comprising: a targeting moiety by conjugation that targets the chimeric protein to a cell.

5. The chimeric protein of claim 4, wherein the targeting moiety is a folate.

6. The chimeric protein of claim 5, wherein the folate is conjugated to the chimeric protein by a disulfide linkage.

7. The chimeric protein of claim 5, wherein the folate is conjugated to the chimeric protein by a malaimde linkage.

8. The chimeric protein of claim 1, further comprising: a modifying group by conjugation that extends the half-life of the chimeric protein

9. The chimeric protein of claim 8, wherein the modifying group is polyethylene glycol.

10. A method of treating an individual with a chimeric protein to induce apoptosis of cells, comprising the steps of: administering, to the individual, a therapeutically effective amount of the chimeric protein, the chimeric protein including a first peptide that is part of a stable human protein and a second peptide being a BH3 domain of BH3-only proteins, the first peptide being one of Calbindin D9k, N-terminal Calmodulin, C-terminal Calmodulin, or Parvalbimin.

11. The method of claim 10, further comprising: co-administrating radiation therapies, chemotherapies, and bio-therapies.

12. The method of claim 10, wherein the chimeric protein has an amino acid sequence selected from the group consisting of Sequence Id No. 1, Sequence Id. No. 2, Sequence Id. No. 3, Sequence Id. No. 4, Sequence Id. No. 5, Sequence Id. No. 6, Sequence Id. No. 7, Sequence Id. No. 8, Sequence Id. No. 9, and Sequence Id. No. 10.

13. The method of claim 10, wherein the administering step includes administering a pharmaceutically acceptable composition that includes a therapeutically effective amount of the chimeric protein.

14. The method of claim 13, wherein the pharmaceutically acceptable composition includes an imaging probe.

15. The method of claim 10, wherein the BH3 domain is selected from the group consisting of BH3-only proteins Bim, Bid, Bad, Bik, Bmf, Hrk, Puma, and Noxia.

16. The method of claim 10, wherein the chimeric protein includes a folate conjugated thereto, the folate being a targeting moiety that targets the chimeric protein to a cell.

17. The method of claim 16, wherein the folate is conjugated to the chimeric protein by one of a disulfide linkage or a malaimde linkage.

18. The method of claim 10, wherein the chimeric protein includes polyethylene glycol conjugated thereto, the polyethylene glycol extending the half-life of the chimeric protein.

19. The method of claim 10, wherein the BH3 domain has a label conjugated thereto.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0028] The detailed description is set forth with reference to the accompanying figures. In the figures, the left-most digit(s) of a reference number identifies the figure in which the reference number first appears. The use of the same reference numbers in different figures indicates similar or identical items or features.

[0029] FIG. 1 is a rendering of a chimeric protein according to the present disclosure.

[0030] FIG. 2 is a graphical representation illustrating the effects of expression of different chimeric proteins in cells according to the present disclosure.

[0031] FIG. 3 is a graphical representation illustrating the effects of chimeric proteins having different host peptides and the BH3 domain of Bid on the apoptosis of SW620 cells according to the present disclosure.

[0032] FIG. 4 is a graphical representation illustrating the effects of chimeric proteins having a Calbindin D9k host peptide and BH3 domains from different BH3-only proteins on the apoptosis of SW620 cells according to the present disclosure.

[0033] FIG. 5 illustrates conjugation of chimeric proteins to a folate according to the present disclosure.

[0034] FIG. 6 is a graphical representation illustrating expression of folate receptors in cancers according to the present disclosure

[0035] FIG. 7 is a graphical representation illustrating the effects of a chimeric protein with a Calbindin D9k host protein, a BH3 domain from Bid or Bim, and a conjugated folate on SW620 cells according to the present disclosure.

[0036] FIG. 8 is a graphical representation illustrating the treatment of SW620 cells with different concentrations of the chimeric protein D-Bid with a disulfide bonded (S—S) folate conjugate according to the present disclosure.

[0037] FIG. 9 is a graphical representation illustrating the effects of chimeric proteins with a Calbindin D9k host protein, BH3 domains from different BH3-only proteins, and a conjugated folate on A549, SW620, and KB cells according to the present disclosure.

[0038] FIG. 10A illustrates the effects (end point tumor sizes) of chimeric proteins (D-Bid) with/without folate conjugation, or with disulfide bond (SS) or malimide (Mal) conjugation on xenograft tumor of SW620 cells according to the present disclosure.

[0039] FIG. 10B is a graphical representation illustrating the effects (tumor growth curve) of chimeric protein (D-Bid) with/without folate conjugation, or with disulfide bond (SS) or malimide (Mal) conjugation on xenograft tumor of SW620 cells according to the present disclosure.

[0040] FIG. 10C a graphical representation illustrating the effects (end point tumor weight) of chimeric protein (D-Bid) with/without folate conjugation, or with disulfide bond (SS) or malimide (Mal) conjugation on xenograft tumor of SW620 cells according to the present disclosure.

[0041] FIG. 11A illustrates conjugation of multi-arm PEGylation agents to a chimeric protein according to the present disclosure.

[0042] FIG. 11B is a graphical representation illustrating the effects (tumor growth curve) of a single folic acid conjugated to different numbers of chimeric protein D-Nox by a multi-arm PEGylation agent according to the present disclosure.

[0043] FIG. 12 is a graphical representation illustrating the effects (endpoint tumor weight) of a single folic acid conjugated to different numbers of chimeric protein D-Nox by a multi-arm PEGylation agent according to the present disclosure.

[0044] FIG. 13 is a graphic representation illustrating the effects of a single folic acid conjugated to different numbers of chimeric protein D-Nox by a multi-arm PEGylation agent according to the present disclosure.

[0045] FIG. 14 is a graphical representation illustrating the synergistic effect of radiation therapy with chimeric proteins including a Calbindin D9k host peptide and a BH3 domain of different BH3-only proteins on SW620 cells according to the present disclosure.

[0046] FIG. 15 is a graphical representation illustrating the synergist effect of oxaliplatin with chimeric proteins including a Calbindin D9k host peptide and a BH3 domain of different BH3-only proteins on SW620 cells according to the present disclosure.

[0047] FIG. 16 is a graphical representation illustrating the treatment of Raw264.7 cells, i.e., macrophage cells, with chimeric proteins including a Calbindin D9k host peptide and a BH3 domain of different BH3-only proteins according to the present disclosure.

DETAILED DESCRIPTION

[0048] Before the present disclosure is described in greater detail, it is to be understood that this disclosure is not limited to particular embodiments described, and as such may, of course, vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to be limiting, since the scope of the present disclosure will be limited only by the appended claims.

[0049] As will be apparent to those of skill in the art upon reading this disclosure, each of the individual embodiments described and illustrated herein has discrete components and features that may be readily separated from or combined with the features of any of the other several embodiments without departing from the scope or spirit of the present disclosure. Any recited method can be carried out in the order of events recited or in any other order that is logically possible.

[0050] Embodiments of the present disclosure will employ, unless otherwise indicated, techniques of medicine, organic chemistry, biochemistry, molecular biology, pharmacology, and the like, which are within the skill of the art. Such techniques are explained fully in the literature.

[0051] Modifications and changes can be made in the structure of the peptides of this disclosure and still obtain a molecule having similar characteristics as the peptide (e.g., a conservative amino acid substitution). For example, certain amino acids can be substituted for other amino acids in a sequence without appreciable loss of activity. Because it is the interactive capacity and nature of a peptide that defines that peptide's biological functional activity, certain amino acid sequence substitutions can be made in a peptide sequence and nevertheless obtain a peptide with like properties.

[0052] In making such changes, the hydropathic index of amino acids can be considered. The importance of the hydropathic amino acid index in conferring interactive biologic function on a peptide is generally understood in the art. It is known that certain amino acids can be substituted for other amino acids having a similar hydropathic index or score and still result in a peptide with similar biological activity. Each amino acid has been assigned a hydropathic index on the basis of its hydrophobicity and charge characteristics. Those indices are: isoleucine (+4.5); valine (+4.2); leucine (+3.8); phenylalanine (+2.8); cysteine (+2.5); methionine (+1.9); alanine (+1.8); glycine (−0.4); threonine (−0.7); serine (−0.8); tryptophan (−0.9); tyrosine (−1.3); proline (−1.6); histidine (−3.2); glutamate (−3.5); glutamine (−3.5); aspartate (−3.5); asparagine (−3.5); lysine (−3.9); and arginine (−4.5).

[0053] It is believed that the relative hydropathic character of the amino acid determines the secondary structure of the resultant peptide, which in turn defines the interaction of the peptide with other molecules, such as enzymes, substrates, receptors, antibodies, antigens, and the like. It is known in the art that an amino acid can be substituted by another amino acid having a similar hydropathic index and still obtain a functionally equivalent peptide. In such changes, the substitution of amino acids whose hydropathic indices are within ±2 is preferred, those within ±1 are particularly preferred, and those within ±0.5 are even more particularly preferred.

[0054] Substitution of like amino acids can also be made on the basis of hydrophilicity, particularly, where the biological functional equivalent peptide or peptide thereby created is intended for use in immunological embodiments. The following hydrophilicity values have been assigned to amino acid residues: arginine (+3.0); lysine (+3.0); aspartate (+3.0±1); glutamate (+3.0±1); serine (+0.3); asparagine (+0.2); glutamine (+0.2); glycine (0); proline (−0.5±1); threonine (−0.4); alanine (−0.5); histidine (−0.5); cysteine (−1.0); methionine (−1.3); valine (−1.5); leucine (−1.8); isoleucine (−1.8); tyrosine (−2.3); phenylalanine (−2.5); and tryptophan (−3.4). It is understood that an amino acid can be substituted for another having a similar hydrophilicity value and still obtain a biologically equivalent, and in particular, an immunologically equivalent peptide. In such changes, the substitution of amino acids whose hydrophilicity values are within ±2 is preferred, those within ±1 are particularly preferred, and those within ±0.5 are even more particularly preferred.

[0055] As outlined above, amino acid substitutions are generally based on the relative similarity of the amino acid side-chain substituents, for example, their hydrophobicity, hydrophilicity, charge, size, and the like. Exemplary substitutions that take various of the foregoing characteristics into consideration are well known to those of skill in the art and include (original residue: exemplary substitution): (Ala: Gly, Ser); (Arg: Lys); (Asn: Gln, His); (Asp: Glu, Cys, Ser); (Gln: Asn); (Glu: Asp); (Gly: Ala); (His: Asn, Gln); (Ile: Leu, Val); (Leu: Ile, Val); (Lys: Arg); (Met: Leu, Tyr); (Ser: Thr); (Thr: Ser); (Tip: Tyr); (Tyr: Trp, Phe); and (Val: Ile, Leu).

[0056] The terms “subject,” “individual,” “patient,” and “host” are used interchangeably herein and refer to any vertebrate, particularly any mammal, and most particularly including human subjects, farm animals, and mammalian pets. The subject may be, but is not necessarily, under the care of a health care professional such as a doctor or veterinarian and may be in need of therapeutic treatment with the compositions of the disclosure.

[0057] The term “stability” as used herein refers to when a peptide essentially retains its physical and chemical stability and integrity upon storage and exposure to what would be inactivating conditions, including but not limited to, oxidation, heat denaturation, peptidase cleavage, and the like, and which would substantially reduce or eliminate the biological activity or structural integrity of the peptide compared to when the peptide has not been subject to such conditions.

[0058] The term “vector” as used herein means a DNA molecule serving as a vehicle capable of stably carrying exogenous genes into host cells. For useful application, a vector should be replicable, have a system for introducing itself into a host cell, and possess selectable markers.

[0059] The present disclosure generally provides proteins, particularly those in an in vivo environment, with extended half-lives and prolonged effectiveness as administered therapeutic agents. Each protein includes a first peptide linked to another, more stable second peptide, thereby forming a fusion peptide with the stability of the second peptide being conferred to the first peptide. For example, the first peptide may substitute for a domain of the second peptide such as an α-helix domain, while still retaining its biological activity.

[0060] FIG. 1 illustrates a chimeric protein having a first/host peptide linked to a second peptide, thereby forming a fused protein with stability of the second peptide being conferred to the first peptide. The protein may be an apoptosis-inducing agent, cancer therapeutic agent, and/or agent for inhibiting cancer metastasis.

[0061] The first/host peptide may be Calbindin D9k (“D”), a N-terminal or C-terminal half-domain of Calmodulin (“Ca”), Parvalbimin (“Pa”), an amino acid sequence variant thereof, or a modified variant thereof. Furthermore, the host peptide may be of human origin. The second peptide is a BH3 domain peptide of different BH3-only proteins such as, for example, Bim (DMRPEIWIAQELRRIGDEFNAYYAR), Bid (EDIIRNIARHLAQVGDSMDRSIPP), Bad (NLWAAQRYGRELRRMSDEFVDSFKK), Bik (CMEGSDALALRLACIADQFHRLHT), Bmf (LQHRAEVQIARKLQCIADQFHRLHT), Hrk (LRSSAAQLTAARLKALGDELHQRTM), Puma (EEQWAREIGAQLRRMADDLNAQYER), and Noxia (PAELEVECATQLRRFGDKLNFRQKLL). The resulting grafted, or chimeric, protein retains biophysical/biochemical properties of the original protein without the BH3 domain attached thereto, and can induce apoptosis of cancerous cells or other cells. Moreover, the protein can contain conservative variants of the peptides explicitly disclosed herein.

[0062] In some instances, the second peptide of the chimeric protein may have the amino acid sequence of a BH3 domain and the first/host peptide may have an amino acid sequence that is part of a human protein (SEQ ID NO. 1-SEQ ID NO. 10), evidenced as follows:

TABLE-US-00001 D-Bim (Sequence Id No. 1)   1 E L M H H H H H H L E M S T K K S P E E  21 L K R I F E K Y A A K E G D P D Q L S K  41 D E L K L L I Q A E F P C L L K G P N T  61 L D D L F Q E L D K N G A G A V S F E D  81 M R P E I W I A Q E L R R I G D E F N A 101 Y Y A * D-Bid (Sequence Id No. 2)   1 E L M H H H H H H L E M S T K K S P E E  21 L K R I F E K Y A A K E G D P D Q L S K  41 D E L K L L I Q A E F P C L L K G P N T  61 L D D L F Q E L D K N G A G A V S F E E  81 D I I R N I A R H L A Q V G D S M D R S 101 I W * Ca-Bim (Sequence Id No. 3)   1 E L M H H H H H H L E M A D Q L T E E Q  21 I A E F K E A F S L F D K D G D G T I T  41 T K E L G T V M R S L G Q N P T E C E L  61 Q D M I N E V D A A G N G T I A F P D M  81 R P E I W I A Q E L R R I G D E F N A Y 101 Y A Ca-Bid (Sequence Id No. 4)   1 E L M H H H H H H L E M A D Q L T E E Q  21 I A E F K E A F S L F D K D G D G T I T  41 T K E L G T V M R S L G Q N P T E C E L  61 Q D M I N E V D A A G N G T I A F P E D  81 I I R N I A R H L A Q V G D S M D R S I 101 W D-Bim1 (Sequence Id No. 5)   1 E L M H H H H H H L E M S T K K S P E E  21 L K R I F E K Y A A K E G D P D Q L S K  41 D E L K L L I Q A E F P C L L K G P N T  61 L D D L F Q E L D K N G D G E V S F E E  81 F Q V L V K K I A Q E L R R I G D E F N 101 A D-Bad (Sequence Id No. 6)   1 H M S T K K S P E E L K R I F E K Y A A  21 K E G D P D Q L S K D E L K L L I Q A E  41 F P C L L K G P N T L D D L F Q E L D K  61 N N L W A A Q R Y G R E L R R M S D E F  81 V D S F K K D-Puma (Sequence Id No. 7)   1 H M S T K K S P E E L K R I F E K Y A A  21 K E G D P D Q L S K D E L K L L I Q A E  41 F P C L L K G P N T L D D L F Q E L D K  61 N E E Q W A R E I G A Q L R R M A D D L  81 N A Q Y E R D-Nox (Sequence Id No. 8)   1 H M S T K K S P E E L K R I F E K Y A A  21 K E G D P D Q L S K D E L K L L I Q A E  41 F P C L L K G P N T L D D L F Q E L D K  61 N P A E L E V E M A T Q L R R F G D K L  81 N F R Q K L L PaN-Bid (Sequence Id No. 9)   1 H M E D I I R N I A R H L A Q V G D S M  21 D R S I P P G F S A T D S F D H K K F F  41 Q M V G L K K K S A D D V K K V F H M L  61 D K D K S G F I E E D E L G F I L K G F  81 C P D A R D L S A K E T K M L M A A G D 101 K D G D G K I G V D E F S T L V A E S PaC-Bid (Sequence Id No. 10)   1 H M S M T D L L N A E D I K K A V G A F  21 S A T D S F D H K K F F Q M V G L K K K  41 S A D D V K K V F H M L D K D K S G F I  61 E E D E L G F I L K G F C P D A R D L S  81 A K E T K M L M A A G D K D G E D I I R 101 N I A R H L A Q V G D S M D R S I P P

[0063] A segment of an α-helix in the host protein having a length, i.e., a number of residues, similar to that of a selected BH3 domain is identified, and a replacement site is located in the loop adjacent to the selected α-helix segment. The BH3 domain sequence replaces a portion of the selected loop, i.e., a few amino acids of the loop are replaced by the end sequence of the BH3 domain. The resultant chimeric protein constructs may be computer simulated by web-based protein structure modeling/prediction programs to find the best construes based on, for example, stability and surface exposure of the BH3 domain.

[0064] The chimeric protein or chimeric nanoparticle includes a protein with various functionalities by combining a BH3 domain variant and a host protein based on a genetic engineering and a protein engineering technique. For example, the BH3 domain peptide may be grafted into a stable human host protein, e.g., Calbindin D9k, Calmodulin Half Domain, or Human Parvalbimin, on the basis that grafting the BH3 domain peptide into a stable host protein would stabilize the secondary structure of the peptide and the entire protein. In another example, a Calbindin D9k host protein, or a portion thereof, includes a BH3 peptide. The BH3 peptide was grafted into the Calbindin D9k host protein by replacing a C-terminal helix. A protein agent according to the present disclosure may therefore be used to treat both cancer and targeted to specific cancer cells. For instance, a chimeric protein having a BH3 peptide can induce apoptosis of a target cell, e.g., a cancer cell.

[0065] FIG. 2 illustrates the effects of expression of different chimeric proteins in cells. All the BH3 domains tested were effective in inducing cell apoptosis when expressed in the cells. The indicated proteins were expressed in the indicated cells. Expression levels were confirmed by immunoblots using antibodies against individual host proteins. Cell viability was measured by cell counting 48 hours after exogenous expression of the indicated proteins. Vector (“Vec”) expression cells were used as a reference (100% cell viability). The error bars indicate standard deviations across five repeating experiments.

[0066] FIG. 3 illustrates the effects of chimeric proteins having different host peptides and the BH3 domain of Bid on the apoptosis of SW620 cells. As indicated, Calbindin D9k was the most effective host peptide in inducing apoptosis. The SW620 cells were treated with 5 μM of the indicated proteins. The proteins were conjugated to folate by a disulfide bond via a 5 kDa PEG. Cell viability was measured by cell counting 48 hours after treatment with the indicated proteins. Buffer treated cells were used as a reference (100% cell viability). The error bars indicate standard deviations across five repeating experiments.

[0067] FIG. 4 illustrates the effects of chimeric proteins having a Calbindin D9k host peptide and different BH3 domains on the apoptosis of SW620 cells. As indicated, the chimeric protein containing the BH3 domain of Noxia (“Nox”) was the most effective in inducing apoptosis. The SW620 cells were treated with 5 μM of the indicated proteins. The proteins were conjugated to folate by a disulfide bond via a 5 kDa PEG. Cell viability was measured by cell counting 48 hours after treatment with the indicated proteins. Buffer treated cells were used as a reference (100% viability). The error bars indicate standard deviations across five repeating experiments.

[0068] The chimeric protein may include a targeting moiety such as, for example, a folate. The use of a folate is beneficial in targeting the chimeric protein to cells having one or more folate receptors or cells expressing excessive amounts of folate receptors. The folate may be attached to the protein by a S—S bond, disulfide bridge, or another type of covalent linkage via, for example, a Cys residue. With a disulfide bond, the overall connectivity is R-S-S-R. The use of a disulfide bridge improves the delivery of the protein to target cells. A protein of the disclosure may exhibit 20 fold enhanced targeting ability. Conjugation of the chimeric protein to folate, as disclosed herein, is illustrated in FIG. 5. Other targeting moieties, include but are not limited to molecules interact with cell surface receptors and trigger endocytosis (e.g., gastrin-releasing peptide and its derivatives, somastostatin and its derivatives, such as Octreotide, Affibody for HER2, aptamer for various growth factor receptors, vasoactive intestinal peptide, and others.

[0069] FIG. 6 illustrates expression of folate receptors in cancers. Advanced and difficult-to-treat cancers overexpress folate receptors. Furthermore, folate receptor expression correlates with poor prognosis.

[0070] FIG. 7 illustrates the effects of a chimeric protein with a Calbindin D9k host protein, a Bid or Bim BH3 domain, and a conjugated folate on SW620 cells. The SW620 cells were treated with 5 μM a chimeric protein with D-Bid (open bar) or D-Bim (filled bars). The proteins were conjugated to folate by a di-sulfide (S—S) or malaimde (MAL) bond via a 5 kDa PEG. NO-Folate indicates the cells treated with proteins not containing a conjugated folate. Cell viability was measured by counting cells 48 hours after treatment with the indicated proteins. Buffer treated cells were used as a reference (100% viability). The error bars indicate standard deviations across five repeating experiment. As FIG. 7 evidences, the di-sulfide bonded conjugate produced the lowest cell viability, i.e., it had the greatest impact upon cell apoptosis.

[0071] FIG. 8 illustrates the treatment of SW620 cells with different concentrations of the chimeric protein D-Bid with a disulfide bonded (S—S) folate conjugate. Cell apoptosis was measured 48 hours after the treatment by Tunnel staining using a Tunnel kit. Cell apoptosis was expressed as percentage apoptosis by counting positive stains vs total cell number (means of six counting) and normalized to that of the buffer treated cells. EC.sub.50 is estimated at around 2.2 μM by 50% cell apoptosis under the treatment.

[0072] FIG. 9 illustrates the effects of chimeric proteins with a Calbindin D9k host protein, different BH3 domains, and a conjugated folate on A549, SW620, and KB cells. As indicated, KB cells had high folate receptor levels, SW620 cells had medium folate receptor levels, and A549 cells had very low folate receptor levels. Furthermore, apoptosis induction has a strong folate receptor dependence. The A549, SW620, and KB cells were treated with 5 μM of the proteins. The proteins were conjugated to folate by a disulfide bond via a 5 Kda PEG. Cell viability was measured by cell counting 48 hours after treatment with the indicated proteins. Buffer treated cells were used as a reference (100% cell viability). The error bars indicate standard deviations across five repeating experiments.

[0073] FIGS. 10A, 10B, and 10C illustrate the effects of folate conjugated chimeric proteins on SW620 cells. SW620 cells (1×10.sup.7) were inoculated in a nude mouse. At 18 days after inoculation, tumor growth was measured at around 290 mm.sup.3. The mice were then treated with daily doses of 10 mg/kg of the indicated proteins via i.p. injection. These daily treatments were stopped after 11 days. All mice were killed 32 days after tumor inoculation. The tumors were sliced out and weighed. Tumor volumes were measured and calculated by:

Tumor Volume=Π/6×(width).sup.2×length

D-Bid is the protein with a folate conjugate, D-Bid/SS is the protein with a disulfide bonded folate conjugate, and D-Bid/MAL is the protein with a malaimde bonded folate conjugate. The error bars indicate standard deviations across five mice.

[0074] FIG. 11A illustrates various multi-arm PEGylation agents. FIGS. 11B (tumor growth curve) and 12 (endpoint tumor weight) illustrate the effects of folate conjugation to varying numbers of chimeric protein D-Nox by a multi-arm PEGylation agent on SW620 cells. Treatment of the xenograft SW620 cells (6 mice/group) was initiated 5 days after tumor inoculation. Treatment consisted of 10 mg/kg (measured by protein D-Nox) i.p. administrations, with one dose being administered every other day for a total of 10 doses. D-Nox 1 Arm, 2 Arm, and 3 Arm denote the conjugation of one folic acid to 1, 2, and 3 D-Nox proteins respectively. The error bars indicate standard deviations across 6 mice.

[0075] FIG. 13 illustrates the effects of folate conjugation to varying numbers of chimeric protein D-Nox by a multi-arm PEGylation agent on SW620 cells. The SW620 cells were treated with 5 μM (open bars) or 10 μM (filled bars) of the chimeric protein (measured by protein D-Nox) D-Nox 1 Arm, 2 Arm, 3 Arm, or buffer. 1 Arm, 2 Arm, and 3 Arm denote the conjugation of one folic acid to 1, 2, or 3 D-Nox proteins respectively by S—S bonds. Cell viability was measured by staining and is represented as percentage of treated cells.

[0076] The protein may be modified to extend, even further, their half-lives by conjugating a modifying group such as, for example, polyethylene glycol (“PEG”) to the chimeric protein. Conjugation of the modifying group may include identifying a residue or residues that can be substituted by Cys and to provide an attachment site for the modifying group.

[0077] Furthermore, a label may be attached to the second peptide of the chimeric protein.

[0078] When administering the chimeric protein to a subject animal or human, the subject animal or human may receive an effective dose of the chimeric protein in conjunction with a pharmaceutically acceptable carrier, thereby resulting in a pharmaceutically acceptable composition. The pharmaceutically acceptable composition may include an imaging probe.

[0079] The chimeric protein may function as an inducible apoptosis system to provide a universal cell ablation system for use in mammalian cells and organisms that allow the study of the biological function of selected cells or a cell type in the mammalian body and thereby the creation of a wide range of animal models of human diseases. Such an inducible apoptosis system is beneficial for all applications requiring its universal activation in any organ and any cell type of the mammalian body, including the brain. It is to be noted that the non-human transgenic animal can be used to study the function of cells, e.g. in mice, by inducible apoptosis. For this purpose the coding region of the recombinant or chimeric proteins may be combined with suitable sequences, for example a cell type specific promoter region, and the protein transgene may be inserted into the mouse germline by pronuclear injection or other methods known in the art.

[0080] The protein according to the present disclosure may be co-administered with another form of therapy. When referring to the treatment of cancer, the term “co-administering” and derivatives thereof as used herein means either simultaneous administration or any manner of separate sequential administration of an agent other than the protein agent, as described herein, and at least one chemotherapeutic agent and a further active ingredient or ingredients, known to be useful in the treatment of cancer, including chemotherapy and radiation treatment. The term further active ingredient or ingredients, as used herein, includes any compound or therapeutic agent known to or that demonstrates advantageous properties when administered to a patient in need of treatment for cancer. If the administration is not simultaneous, the compounds are administered in a close time proximity to each other. Furthermore, it does not matter if the compounds are administered in the same dosage form, e.g. one compound may be administered topically and another compound may be administered orally.

[0081] FIG. 14 illustrates the synergistic effect of radiation therapy with chimeric proteins including a Calbindin D9k host peptide and different BH3 domains on SW620 cells. The SW620 cells were treated with 5 μM of the indicated proteins for 1 hour. The cells were then irradiated, with radiation, by 10 Gray (filled bars) or without radiation (open bars). Cell viability was measured by cell counting 24 hours after the radiation treatments were started. Buffer treated without radiation cells were used as a reference (100% viability). The error bars indicate standard deviations across five repeating experiments.

[0082] FIG. 15 illustrates the synergist effect of oxaliplatin with chimeric proteins including a Calbindin D9k host peptide and different BH3 domains on SW620 cells. The SW620 cells were treated with 5 μM of the indicated proteins and with (filled bars) or without (open bars) 20 μM of oxaliplatin. Cell viability was measured by cell counting 48 hours after treatment with the indicated proteins. Buffer treated without oxaliplatin cells were used as a reference (100% viability) The error bars indicate standard deviations across five repeating experiments.

[0083] The therapeutic protein may be used to treat Inflammatory Diseases such as rheumatoid arthritis, which is mediated by induction of macrophage apoptosis. FIG. 16 illustrates the treatment of Raw264.7 cells, i.e., macrophage cells, with chimeric proteins including a Calbindin D9k host peptide and different BH3 domains. As indicated, the chimeric proteins were effective in inducing apoptosis of activated macrophage cells. The Raw264.7 cells were treated with 5 μM of the indicated proteins, which were conjugated to folate via a S—S bond. Cell viability was measured by cell counting 48 hours after treatment with the indicated proteins. Buffer treated cells were used as a reference (100% viability). The error bars indicate standard deviations across five repeating experiments.

[0084] Treatment may be accomplished with varying doses as well as dosing regimens, provided the combination of the doses is effective at treating any one or more of a number of therapeutic parameters. These treatment regimens may alternatively or may also be based on doses and dosing schedules that maximize therapeutic effects, such as those described herein. A dose of the protein may not be therapeutically effective when administered individually, but may be therapeutically effective when administered in combination with another agent. Thus, the therapeutically effective dose of a combination of the protein and a therapeutically radioactive isotope may comprise doses of individual active agents that, when administered alone, would not be therapeutically effective or would be less therapeutically effective than when administered in combination with each other.

[0085] The target cell of the chimeric protein may be an isolated cell. Furthermore, the target cell may be in a tissue of a subject animal or human. An imaging probe may be administered to the subject animal or human as a pharmaceutically acceptable composition. The binding site of the chimeric protein to the target cell may be a receptor on the surface of the cell through an attached targeting moiety.

[0086] Another aspect of the disclosure relates to a method for inducing apoptosis of a cell expressing a chimeric protein according to the disclosure. The method includes transfection of DNA encoding the chimeric proteins capable of inducing apoptosis of the cell.

[0087] The specific examples disclosed herein are to be construed as merely illustrative, and not limitative of the remainder of the disclosure in any way whatsoever. Without further elaboration, it is believed that one skilled in the art can, based on the description herein, utilize the present disclosure to its fullest extent.

[0088] The disclosed examples are put forth so as to provide those of ordinary skill in the art with a complete disclosure and description of how to perform the methods and use the compositions and compounds disclosed and claimed herein. Efforts have been made to ensure accuracy with respect to numbers e.g., amounts, temperature, etc., but some errors and deviations should be accounted for. Unless indicated otherwise, parts are parts by weight, temperature is in ° C., and pressure is at or near atmospheric. Standard temperature and pressure are defined as 20° C. and 1 atmosphere.

[0089] It should be noted that ratios, concentrations, amounts, and other numerical data may be expressed herein in a range format. It is to be understood that such a range format is used for convenience and brevity, and thus, should be interpreted in a flexible manner to include not only the numerical values explicitly recited as the limits of the range, but also to include all the individual numerical values or sub-ranges encompassed within that range as if each numerical value and sub-range is explicitly recited. To illustrate, a concentration range of “about 0.1% to about 5%” should be interpreted to include not only the explicitly recited concentration of about 0.1 wt % to about 5 wt %, but also include individual concentrations, e.g., 1%, 2%, 3%, and 4%, and the sub-ranges, e.g., 0.5%, 1.1%, 2.2%, 3.3%, and 4.4%, within the indicated range. The term “about” can include ±1%, ±2%, ±3%, ±4%, ±5%, ±6%, ±7%, ±8%, ±9%, or ±10%, or more of the numerical value(s) being modified.