A Polypeptide EXP and its Drug Delivery System as well as Extracellular Vesicle Extraction

Abstract

The present invention “A polypeptide EXP and its drug delivery system as well as extracellular vesicle extraction kit thereof” belongs to the field of biomedical engineering and diagnostics. The amino acid sequence of the polypeptide EXP is set forth in SEQ ID NO. 1. Based on the polypeptide EXP, the present invention also provides a drug delivery system, targeted drug delivery system, enhanced drug delivery vehicle, a drug with enhanced delivery, targeted drug, extracellular vesicle extraction kit, disease diagnostic kit, a method for purifying extracellular vesicles, and use of the polypeptide EXP in pharmacy and diagnostic reagent manufacture.

Claims

1. A polypeptide EXP, characterized in that, its amino acid sequence is shown as SEQ ID NO. 1.

2. A drug delivery system, characterized in that, comprises the polypeptide EXP according to claim 1 and drug delivery vector.

3. The drug delivery systems according to claim 2, characterized in that, the EXP binds to the drug delivery vector via CD63 and/or CD81 protein; preferably, the drug delivery vector is the vector expressing or carrying CD63 and/or CD81; the vector expressing or carrying CD63 and/or CD81 is selected from exosome, extracellular microvesicle; exosome—, extracellular microvesicle-expressing or attaching CD63 and/or CD81 protein, liposome, nanoparticle.

4. The drug delivery system according to claim 2, further comprising a pharmacodynamically active molecule; Said pharmacodynamically active molecule are selected from polypeptide, nucleic acid, and small molecular compound which can be covalently conjugated to EXP; preferably, the polypeptide that can be covalently conjugated to EXP is selected from muscle-targeting peptide M12, liver cancer-targeting peptide P47, brain-targeting peptide RVG and other functional polypeptides, for example, N1ND; preferably, the small molecular compound which can be covalently conjugated to EXP is selected from Phosphorodiamidate Morpholino Oligomer (PMO); preferably, the nucleic acid which can be covalently conjugated to EXP is selected from neutral, uncharged PMO or PNA.

5. A targeted drug delivery system, characterized in that, comprises the polypeptide EXP according to claim 1, drug delivery vector and targeting peptide.

6. The targeted drug delivery system according to claim 5, characterized in that, the polypeptide EXP binds to drug delivery vector via CD63 and/or CD81 site; preferably, the drug delivery vector is the vector that can express or carry CD63 and/or CD81; the vector that can express or carry CD63 and/or CD81 is selected from exosome, extracellular microvesicle; exosome—, extracellular microvesicle-attaching CD63 and/or CD81 protein, liposome, nanoparticle.

7. The targeted drug delivery system according to claim 5, further comprising a pharmacodynamically active molecule; said pharmacodynamically active molecule is selected from polypeptide and nucleic acid which can be covalently conjugated to EXP; preferably, said polypeptide which can be covalently conjugated to EXP is selected from M12, P47, RVG or N1ND; preferably, said nucleic acid that can be covalently conjugated to EXP is selected from PMO.

8. An enhanced drug delivery vector, characterized in that, is a drug delivery vector which is linked or modified by the polypeptide EXP according to claim 1.

9. The enhanced drug delivery vector according to claim 8, characterized in that, the polypeptide EXP binds to drug delivery vector via CD63 and/or CD81 protein; preferably, the drug delivery vector is a vector that can express or carry CD63 and/or CD81; the vector that can express or carry CD63 and/or CD81 is selected from exosome, extracellular microvesicle, and plasmid that can express CD63 and/or CD81.

10. A drug with enhanced delivery, characterized in that, the effective component of the drug is loaded on the enhanced drug delivery vector of claim 8.

11. A targeted drug, characterized in that, the drug composition of the targeted drug is included in any of the targeted drug delivery system of claim 6.

12. An extracellular vesicle extraction kit, characterized in that, comprises the polypeptide EXP according to claim 1.

13. The extracellular vesicle extraction kit according to claim 12, characterized in that, also comprises reagent for extracting and purifying extracellular vesicle; Preferably, the polypeptide EXP is coated on nickel bead, or magnetic bead, or covalently linked to microsphere or nanobead by mature chemical processing.

14. The extracellular vesicle extraction kit according to claim 12, wherein the extracellular vesicle is selected from exosome and/or microvesicle.

15. A disease diagnosis kit, characterized in that, the disease diagnosis marker is exosome surface protein molecule and disease-related specific protein molecule, for example, liver cancer specific antigen AFP; the kit includes the polypeptide EXP according to claim 1.

16. The disease diagnosis kit according to claim 15, characterized in that, also includes reagent for extracting and purifying exosome; preferably, the reagent for purifying exosome includes: nickel bead coated with the polypeptide EXP; binding buffer of pH7.4 with a formula of 50 mM imidazole, 500 mM sodium chloride, 20 mM disodium hydrogen phosphate; washing solution of pH7.4 with a formula of 75 mM imidazole, 500 mM sodium chloride, 20 mM disodium hydrogen phosphate; eluent of pH7.4 with the formula of 500 mM imidazole, 500 mM sodium chloride, 20 mM disodium hydrogen phosphate; preferably, the exosome is selected from exosome derived from human serum, and/or exosome derived from human urine, and/or free exosome derived from other source, and/or exosome from cell culture supernatant.

17. A method for purifying extracellular vesicle, characterized in that, comprises binding or capturing the extracellular vesicle with the polypeptide EXP according to claim 1.

18. The method for purifying microvesicle according to claim 17, comprises: Step 1, His labeled EXP and CP05 (100 μg) is respectively combined with 40 μL nickel bead in 200 μL binding buffer, and incubated for 1 h at 4° C.; Step 2, nickel bead which has been coated with His-EXP and His-CP05 is added to 1 mL pre-centrifuged serum (4400 g, centrifugate for 20 min, 13000 g, centrifugate for 5 min) and incubated at 4° C. for 30 min; Step 3, discard the serum and wash off a nonspecific binding with the washing solution, 10 min/times, 3 times; Step 4, 100 μL eluent is used to extract the extracellular vesicle.

19. The method for purifying extracellular vesicle according to claim 17, wherein the extracellular vesicle is selected from exosome and/or microvesicle.

20. Use of the polypeptide EXP according to claim 1 in the pharmacy.

21. The use according to claim 20, characterized in that, comprises the polypeptide EXP is connected with the drug delivery vector to obtain an enhanced drug delivery vector based on the peptide EXP-vector complex.

22. The use according to claim 21, characterized in that, also comprises the drug molecule is connected with the polypeptide EXP-vector complex to obtain a drug based on the drug molecule-polypeptide EXP-vector complex.

23. The use according to claim 22, characterized in that, also comprises the targeting peptide is further connected with the drug molecule-polypeptide EXP-vector complex to obtain a targeted drug.

24. The use of the polypeptide EXP according to claim 1 in a preparation of disease diagnosis reagent.

25. The use according to claim 24, characterized in that, comprises the polypeptide EXP is connected with exosome.

26. The use of claim 25, characterized in that, the exosome is selected from exosomes derived from human serum, human urine or other source.

Description

DESCRIPTION OF DRAWINGS

[0064] FIG. 1 shows the binding efficiency of anchoring polypeptide with exosome. The present invention shows three polypeptides with different sequences, EXP (CRHKMWTVKSRL), 39880 (CKHNQWTVTSRL) and 39881 (SQCSVSTKL). The FAM-labeled peptides EXP, CP05, 39880, 39881 were respectively co-incubated with exosome from differentiated muscle cells C2C12 (dC2C12), and the binding efficiency of different polypeptides with exosome was detected by flow cytometry.

[0065] Each sign in the figure represents the detection results of the following sequences: EXO represents exosomes derived from murine myotubes; CP05 represents the polypeptide which is recorded in the prior art Chinese patent No. CN201510520565.7; EXP represents the polypeptide of the present invention (SEQ ID NO. 1). 39880 and 399881 respectively represent two other variants of CP05. (A) Flow cytometry to detected the binding efficiency of different peptides with exosomes. It's shown by the results that EXP demonstrated the highest binding efficiency to exosomes, up to 95.5%, indicating the strongest binding capacity. (B) Flow cytometry to detected the capacity to enter cells of different peptides mediated by exosome. The equivalent amount FAM-labeled polypeptides were incubated with exosome derived from dC2C12 and added into C2C12 cells, and the capacity of enter cells was detected 24 hours later. It's shown by the results that 65.6% of EXO-EXP entered cells whose capacity is highest. (C) Quantitative analysis of different peptides entering cells mediated by exosome. It's shown by the results that the ratio of EXO-EXP positive C2C12 cells is highest, which is twice as mush as EXOCP05, which points out that the capacity of EXP enter cells mediated by EXO is higher than CP05 and other variants, and suggests that EXP bears stronger binding ability to exosomes than CP05. (D) the binding efficiency of different amount gradients of CP05 and EXP to the equivalent amount of exosomes was detected by Flow cytometry to. Different amounts of EXP and CP05 (0.03 μg, 0.06 μg, 0.3 μg) were co-incubated with exosomes (10 μg), and their binding efficiency was compared by flow cytometry. It's shown by the results that under different amount gradients, the binding efficiencies of EXP and exosome are all higher than that of CP05, and EXP exhibited a higher binding advantage particularly at low concentration.

[0066] FIG. 1A shows a flow cytometry to detected the binding efficiency of different peptides with exosomes.

[0067] FIG. 1B shows a flow cytometry to detected the capacity to enter cells of different peptides mediated by exosome.

[0068] FIG. 1C shows a quantitative analysis of different peptides entering cells mediated by exosome.

[0069] FIG. 1D shows the binding efficiency of different amount gradients of CP05 and EXP to the equivalent amount of exosomes was detected by Flow cytometryto.

[0070] FIG. 2 shows the results for detecting the binding stability of CP05 and EXP with exosomes. The intracellular co-localization of CP05 and EXP with exosomes was examined with confocal microscopy at different timepoints. FAM-labeled CP05 and EXP were incubated with DiI-labeled exosomes and then added into C2C12 cells. The co-localization of peptides and exosomes were observed with confocal microscopy, and FRET was used to examine the binding capacity of peptides to exosomes at different timepoints (6 hours, 12 hours, 24 hours, 48 hours).

[0071] The meanings of the signs in the figure are as follows: DAPI means staining result for nuclei by DAPI, Peptide (488,520) refers to the excitation and emission wavelength of FAM-labeled CP05 and EXP; EXO (Dil)(540,620) refers to the excitation and emission wavelength for DiI-labeled exosomes; Merge is the superposition of above three staining results; FRET means fluorescence resonance energy transfer. Optical energy resonance transfer is an energy transfer phenomenon between two fluorescent molecules that are very close to each other. When the emission spectrum of the donor fluorescent molecule overlaps with the absorption spectrum of the acceptor fluorescent molecule, and the distance between two molecules is within the range of 10 nm, a non-radioactive energy transfer occurs. In the figure, the FAM-Peptide is the donor fluorescent molecule and DiI-EXO is the acceptor fluorescent molecule. FRET (488, 620) represents the excitation of FAM-Peptide and the absorption wavelength of DiI-EXO. EXOCP05 is the staining result of exosomes combined with CP05 sequence which is recorded in the prior art Chinese Patent No. CN201510520565.7, and EXOEXP refers to the staining result of the combination of EXP of the present invention and exosomes. It's shown by the results that there was co-localization between EXP and CP05 with exosomes in cells at different timepoints. The co-localization of CP05 and EXO in the cells reached the peak in 12 hours, and reduced after 24 hours. Most of CP05 degraded at 48 hours, and the co-localization of CP05 and EXO was significantly reduced. However, as to EXP, the co-localization of EXP and EXO was still detectable in cells at 48 hours, which suggests a stronger binding stability of EXP with EXO than CP05.

[0072] FIG. 3 shows the detecting results on the capacity of the competitive binding of CP05 and EXP to exosomes. AF750 (APC-Cy7)-labeled CP05 and FAM-labeled CP05 or EXP were co-incubated with exosomes at ratios of 1:1 or 1:5 (mass ratio), and the binding efficiency was detected with flow cytometry. It's shown by the results that when EXP and CP05 were incubated with exosomes at the same time, EXP could compete with CP05 to combine with exosomes, thus reducing the binding efficiency of CP05 and exosomes. (A) Flow cytometry to detect the binding efficiency of EXP or CP05 to exosomes. EXO was used as negative control; EXOCP05 is the binding efficiency of CP05 (FAM, af750) separately labeled by different fluorescence labeling with exosomes. EXOEXP is the binding efficiency of FAM labeled EXP andexosomes.1:1, 1:5, 1:10 means different mass ratios of AF750 and FAM-EXP/FAM-CP05 are respectively as 1:1, 1:5, 1:10. It's shown by the results of flow cytometryto that the binding efficiency of CP05 alone with EXO was about 70%, while that of EXP and exosomes was 91.5% (flow cytometry to chart: the first line). When CP05 and EXP was co-incubated with exosome, it's discovered by detecting their binding efficiency that (flow cytometry to chart: the middle row), And the binding efficiency of EXOCP05 (AF750) reduced after mass of EXP was increased to 5-fold and 10-fold higher than that of CP05. However, it's found by comparing different fluorescence CP05 molecules (flow cytometry to chart: the third line) that, the binding efficiency of EXOCP05 (AF750) remained unchanged with increasing the mass ratio of FAM-CP05. It is suggested that EXP can competitively bind the binding sites of CP05 and exosomes, resulting in the decrease of binding efficiency. (B) shows quantitative analysis of the binding efficiency of polypeptides to exosomes. Different fluorescence-labeled CP05 (APC-Cy7, FAM) were co-incubated with exosomes, their binding efficiency is detected with flow cytometry. CP05 (AF750) means the binding efficiency of wherein exosome with CP05 (AF750). CP05 (FAM) means the binding efficiency of wherein exosome with CP05 (FAM); EXP (FAM) means the binding efficiency of wherein exosome with EXP (FAM). It's indicated by the results (as shown in the first row of the table) that the binding efficiency of CP05 (AF750) to exosomes remained the same (from 57% to 63.1%) when amounts of FAM-CP05 was increased after exosome and CP05 (AF750) were co-incubated with CP05 (FAM). However, after exosome and CP05 (AF750) were co-incubated with EXP (FAM) (the second row of the table), the binding efficiency of CP05 (AF750) was decreased (from 66.9% to 48.4%) as amounts of FAM-EXP was increased.

[0073] FIG. 3A shows a flow cytometry to detect the binding efficiency of EXP or CP05 to exosomes.

[0074] FIG. 3B shows a quantitative analysis of the binding efficiency of polypeptides to exosomes.

[0075] FIG. 4 shows target detection of EXP. (A) Silver staining and Western blot were used to detect the interest proteins band obtained by co-immunoprecipitation. Flag-tagged CP05 or EXP was incubated with anti-flag coated beads, and followed by co-incubation with cell lysates after removing the free peptides which were unconjugated with beads. The specific enriched proteins in the cell protein lysate were fished by using the polypeptide. Then the size distribution of the fishing strip was detected by silver staining, and the expression of different Tetraspanin family proteins in the fishing strip was detected by Western blot. It's shown by the results that there were distinct protein bands with sizes of about 45 kD and 25 kD appeared in the EXP group in comparison to the control group. It's confirmed by the western blot results that these the distinct protein bands are CD63 and CD81. (B) Immunoprecipitation was used to catch the target of EXP. The results are the same as above.

[0076] FIG. 4A shows that silver staining and Western blot were used to detect the interest proteins band obtained by co-immunoprecipitation.

[0077] FIG. 4B shows that immunoprecipitation was used to catch the target of EXP.

[0078] FIG. 5 shows the results of detecting the binding ability of EXP to exosomes from different sources, and the binding efficiency of CP05 and EXP with exosomes from different sources detected by Flow cytometry. FAM-labeled CP05 or EXP was co-incubated with exosomes derived from murine myotubes (EXOmyotube), cardiac sphere cells (CDC)(EXOCDC) and human serum (EXOserum), and the binding efficiency was detected with flow cytometry. It's shown by the results that the binding efficiency of CP05 to exosomes from different sources is about 70%, and the binding efficiency of the same amount of EXP with exosomes from corresponding sources was about 90%. When incubated with exosomes from different sources, EXP showed higher binding efficiency.

[0079] FIG. 6 shows exosomes morphology identification and application ability detection of exosomes in EXP captured serum. (A) Nano sight was used to detect the particle size of exosomes in serum captured by CP05 and EXP. It's shown by the results that the particle size of exosomes captured by EXP was about 50 nm, whose homogeneity was higher than that of exosomes recovered by ultra separation. (B) shows methods of CP05 and EXP capture and comparison of the number of exosomes in the equivalent ultra separated serum; (C) The morphology and size of exosomes captured by CP05 and EXP were detected by transmission electron microscopy. It's shown by the results that exosomes captured by EXP has typical bi-layer structure, and the size of exosomes captured by EXP was smaller than that of exosomes recovered by ultrafiltration. (D) Western blot was used to detect the marker protein capturing exosome. It's shown by the results that EXP captured marker proteins CD63, CD81 and HSC70 expressed by exosome. (E) The binding efficiency of exosomes in serum with CP05 and EXP was detected. It's shown by the results that: exosomes recovered by EXP could combine with CP05 and EXP, and the binding efficiency of EXP with recovered exosomes was 95.9%, much higher than that of CP05 (76.8%). (F) detection of the binding efficiency of exosome in serum with CP05 and EXP, it's shown by the results that the capture efficiency of exosomes in serum by EXP was 93.5%, higher than 83.3% of CP05.

[0080] FIG. 6A shows that Nano sight was used to detect the particle size of exosomes in serum captured by CP05 and EXP.

[0081] FIG. 6B shows methods of CP05 and EXP capture and comparison of the number of exosomes in the equivalent ultra separated serum.

[0082] FIG. 6C shows that the morphology and size of exosomes captured by CP05 and EXP were detected by transmission electron microscopy.

[0083] FIG. 6D shows that Western blot was used to detect the marker protein capturing exosome.

[0084] FIG. 6E shows the binding efficiency of exosomes in serum with CP05 and EXP.

[0085] FIG. 6F shows a detection of the binding efficiency of exosome in serum with CP05 and EXP.

[0086] FIG. 7 shows functional evaluation of EXP-mediated exosomes as delivery vector. Antisense oligonucleotide drugs PMO were covalently conjugated to CP05 or EXP to form the peptide-PMO conjugates CP05PMO and EXPPMO. CP05PMO and EXPPMO were co-incubated with exosomes to form EXOCP05PMO and EXOEXPPMO composition, in order to mediate in restoring the expression of dystrophin protein inmdx mousetibialis anterior (TA) muscles. Wherein, PMO means local injection of 2 g PMO into tibialis anterior muscles; CP05PMO means local injection of 2 μg CP05PMO into TA muscles; EXPPMO means local injection of 2 μg EXPPMO into TA muscles; EXOCP05PMO means that 2 μg CP05PMO was co-incubated with 2 g exosomes and injected into TA muscles, EXOEXPPMO means that 2 μg EXPPMO was co-incubated with 2 g exosomes and injected into TA muscles. (A) immunohistochemistry was used to detect distribution of dystrophin-positive myofibersinmuscle fiber tissues. (B) Quantitative analysis on the number of dystrophin-positive myofibers after injection of different compounds in mdx mouse TA tissue. It's shown by the results that recovery of dystrophin myofibers of EXOEXPPMO group is higher than that of EXOCP05PMO group, which suggests that EXP can mediate high-efficient PMO delivery. (C) Western blot is used to detect and compare the recovery level of dystrophin protein after treated with EXOEXPPMO or EXOCP05PMO, wherein C57 means TA tissue protein of wild-type mouse, mdx means dystrophin deficient TA tissue protein without treat. (D) Quantitative analysis on recovery level of dystrophin protein treated with EXOEXPPMO or EXOCP05PMO. The results is consistent to immunohistochemistry and staining results, which showed higher levels of dystrophin expression in EXOEXPPMO treating group than EXOCP05PMO group.

[0087] FIG. 7A shows a distribution of dystrophin-positive myofibers in muscle fiber tissues.

[0088] FIG. 7B shows a quantitative analysis on the number of dystrophin-positive myofibers after injection of different compounds in mdx mouse TA tissue.

[0089] FIG. 7C shows a recovery level of dystrophin protein after treated with EXOEXPPMO or EXOCP05PMO.

[0090] FIG. 7D shows a quantitative analysis on recovery level of dystrophin protein treated with EXOEXPPMO or EXOCP05PMO.

[0091] FIG. 8 shows functional test of EXP mediated MV (microcapsules) as drug delivery vectors. (A) Western blot is used to identify and compare the expression of biomarker proteins of MV and exosomes. It's shown by the results that Tetraspanin family proteins like CD81, CD9 and CD63 were expressed in MV, but mitochondrial marker protein Cytochrome C was not expressed. (B) particle size distribution of MV from different sources were detected by Nanosight. MVmyot means microvesicles derived from differentiated muscle cells; MVurine means microvesicles derived from urine. (C) Examination of the binding efficiency of EXP and CP05 to MVmyo was detected by flow cytometer. It's shown by the results that the binding efficiency of EXP to MVmyotis significantly higher than that of CP05. (D) shows local test of PMO drug delivered by EXP mediated MV in tibialis anterior muscles, and recovery of dystrophin positive muscle fiber was detected by immunohistochemical staining. (E) Western blot was used to detect the recovery of dystrophin protein expression after MVEXPPMO treatment. (F) shows quantitative analysis of dystrophin protein after treated with MVEXPPMO.

[0092] FIG. 8A shows a expression of biomarker proteins of MV and exosomes.

[0093] FIG. 8B shows a particle size distribution of MV from different sources.

[0094] FIG. 8C shows a binding efficiency of EXP and CP05 to MVmyo.

[0095] FIG. 8D shows a local test of PMO drug delivered by EXP mediated MV in tibialis anterior muscles, and recovery of dystrophin positive muscle fiber.

[0096] FIG. 8E shows a recovery of dystrophin protein expression after MVEXPPMO treatment.

[0097] FIG. 8F shows a quantitative analysis of dystrophin protein after treated with MVEXPPMO.

[0098] FIG. 9 shows the targeted transport of exosomes delivered by EXP mediated brain target peptide RVG. TA—tibialis anterior muscle; Q—quadriceps; G—gastrocnemius; T—triceps; H—heart; S—spleen; K—kidney; Lu—lung; Li—liver; Br—brain; In—small intestine.

EMBODIMENTS

[0099] The present invention will be further illustrated with the following figures and specific examples, but the protection scope is not limited by these examples. Unless otherwise specified, the experimental procedures in which the specific conditions are not indicated in the following examples are generally carried out according to routine procedures, or conditions which can be inferred by those skilled in the art within the knowledge range, or according to the conditions recommended by the manufacturer. The reagents and apparatus referred to in the following examples are typically commercially available products, or products that can be obtained by other publicly available means.

Description of the Main Apparatus Involved in the Following Examples:

[0100]

TABLE-US-00001 Instrument name Company/country Flow cytometry BD FACS ArialII/USA Ultra clean bench Airtech/China high speed refrigerated centrifuge Eppendorf/Germany Electric Heating constant Temperature Tianjin Zhonghuan Experimental Electric Incubator Furnace Company limited./China High pressure steam sterilizer Sanyo company/Japan Positive fluorescence microscope Olympus BX51/Japan Inverted fluorescence microscope Olympus IX71/Japan Confocal fluorescence microscope Olympus Corporation/Japan Automatic microplate reader Bio-Tek Synergy HT/USA −80° C. low temperature refrigerator Sanyo company/Japan −20° C. low temperature refrigerator Haier Company/China Ice maker Grant company/United States Micronuclei acid analyzer NanoDrop 2000c/United States Vertical Gel Tank Bio-Rad/United States

[0101] The 1.sup.st group of examples: The polypeptide EXP of the invention.

[0102] This group of examples provides a polypeptide EXP, characterized in that, its amino acid sequence is set forth in SEQ ID NO. 1.

[0103] The 2.sup.nd group of examples: The drug delivery system of the invention.

[0104] This group of examples provides a drug delivery system, characterized in that, comprises the polypeptide EXP according to any of the Is group of examples and drug delivery vector.

[0105] In some examples, the polypeptide EXP binds to drug delivery vector via CD63 and/or CD81 site.

[0106] Preferably, the drug delivery vector is vector that can express and carry CD63 and/or CD81;

[0107] Preferably, the drug delivery vector can express or carry CD63 and/or CD81 is selected from exosome, extracellular microvesicle, liposome, nanoparticle, and/or, exosome, extracellular microvesicle attaching CD63 and/or CD81 protein.

[0108] In other examples, the drug delivery system also includes: pharmacodynamically active molecule; the pharmacodynamically active molecule is selected from polypeptide, nucleic acid, and small molecule compound that can covalently connect with EXP.

[0109] Preferably, the polypeptide that can covalently connect with EXP is selected from muscle-targeting peptide-M12, liver cancer-targeting peptide-P47, cranial nerve-targeting peptide-RVG and other functional polypeptide, for example, N1ND.

[0110] Preferably, the small molecule compound that can covalently connect with EXP is selected from Phosphorodiamidate Morpholino Oligomer (PMO).

[0111] Preferably, the nucleic acid that can covalently connect with EXP is selected from neutral, uncharged PMO or PNA.

[0112] The polypeptide that can covalently connect with EXP can also be a targeting peptide targeting different tissues, or a functional polypeptide of any sequence. Since peptide synthesis is a very mature technology, EXP is also a kind of peptide, which can be artificially synthesized with any other peptide, and any polypeptide can be synthesized with EXP. This is also the advantage of EXP, which can be synthesized with any sequence of polypeptide through mature artificial polypeptide synthesis technology.

[0113] The 3.sup.rd group of examples: The targeted drug delivery system of the invention.

[0114] The present group of examples provides a targeted drug delivery system, characterized in that, comprises the polypeptide EXP according to any of the 1.sup.st group of examples, drug delivery vector and targeting peptide.

[0115] In some embodiments, the polypeptide EXP binds to drug delivery vector via CD63 and/or CD81 site.

[0116] Preferably, the drug delivery vector is vector that can express or carry CD63 and/or CD81; the vector that can express or carry CD63 and/or CD81 is selected from exosome, extracellular microvesicle, liposome and nanoparticle, exosome, extracellular microvesicle attaching CD63 and/or CD81 protein.

[0117] In further embodiments, said targeted drug delivery system also includes: pharmadynamically active molecule; the pharmadynamically active molecule is selected from polypeptide and nucleic acid molecule that can covalently connect with EXP;

[0118] Preferably, the polypeptide that can covalently connect with EXP is selected from M12, P47, RVG or N1ND.

[0119] Preferably, the nucleic acid molecule that can covalently connect with EXP is selected from Phosphorodiamidate Morpholino Oligomer (PMO).

[0120] The 4.sup.th group of examples: the enhanced drug delivery vector of the invention.

[0121] This group of embodiments provides the enhanced drug delivery vector, characterized in that, is drug delivery vector that is linked or modified by the polypeptide EXP according to any of the 1.sup.st group of examples.

[0122] In some embodiments, the polypeptide EXP binds to the drug delivery vector via CD63 and/or CD81 site.

[0123] Preferably, the drug delivery vector is vector that can express or carry CD63 and/or CD81; the vector that can express or carry CD63 and/or CD81 is selected from exosome, extracellular microvesicle, plasmid that can express CD63 and/or CD81.

[0124] The 5.sup.th group examples: a transport enhanced drug of the invention.

[0125] This group of embodiments provides a transport enhanced drug, characterized in that, the effective component of the drug is loaded on the enhanced drug delivery vector according to any of the 4.sup.th group of examples.

[0126] For example, the nucleotide sequence of a specific polypeptide drug HMGN1 and the nucleotide sequence of EXP can be loaded into the gene expression vector (e.g., lentiviral vector: pCDH-CMVpuro-insulin-HMGN1). The polypeptide of HMGN1 and EXP can be expressed through said gene expression vector and binded to CD63/CD81 on drug delivery vector via EXP to form the structure of polypeptide+EXP+drug, i.e., Thus the polypeptide transport enhanced drug can be obtained.

[0127] For short peptide less than 60 amino acids, no gene expression system is needed; for peptides or proteins larger than 60 amino acids, gene expression vectors are needed.

[0128] In other embodiments, nucleic acid drug PMO can be covalently conjugated with EXP to obtain a complex structure PMO-EXP of nucleic acid drug, subsequently PMO-EXP can bind to CD63 and/or CD81 on drug delivery vector via EXP to generate a structure of PMO-EXP-drug delivery vector, namely, nucleic acid transport enhanced drug is obtained.

[0129] The 6.sup.th group of examples: a targeted drug of the invention.

[0130] This group of embodiments provides a targeted drug, characterized in that, the drug composition of the targeted drug is included in the targeted drug delivery system according to any of the 3.sup.rd group of examples.

[0131] For example, PMO covalently conjugated to EXP can be used for treating DMD.

[0132] The 7.sup.th group of examples: An extracellular vesicle recovery kit of the invention.

[0133] This group of embodiments provides a extracellular vesicle recovery kits characterized in that, comprises the polypeptide EXP according to any of the 1 group of examples.

[0134] In further embodiments, said extracellular vesicle recovery kit also includes conventional reagent for recovering and purifying extracellular vesicle.

[0135] Preferably, said conventional reagent for recovering and purifying extracellular vesicle includes:

[0136] More preferably, the polypeptide EXP is coated on nickel bead, or magnetic bead, or covalently linked to microsphere or nanobead by mature chemical processing.

[0137] In some embodiments, the extracellular vesicle is selected from exosome and/or microvesicle.

[0138] The 8.sup.th group of examples: A disease diagnosis kit of the invention

[0139] This group of embodiments provides a disease diagnosis kit, characterized in that, the disease diagnosis markers are exosome surface protein molecule and disease-related specific protein molecule, such as liver cancer specific antigen AFP; the kit includes the polypeptide EXP according to any of the 1.sup.st group of examples.

[0140] For example, for the diagnosis of tumor or muscle dystrophic patients, just like CP05 in the prior art, EXP can be adhered to the magnetic bead to capture free exosome, and whether suffering from the disease can be diagnosed by detect concentration of exosome.

[0141] In further embodiments, said diagnostic kit also comprises reagent for recovering and purifying exosome.

[0142] Preferably, the reagent for purifying exosome includes: nickel bead coated with polypeptide EXP; binding buffer of pH7.4 with a formula of 50 mM imidazole, 500 mM sodium chloride, 20 mM disodium hydrogen phosphate; washing solution of pH7.4 with a formula of 75 mM imidazole, 500 mM sodium chloride, 20 mM disodium hydrogen phosphate; eluent of pH7.4 with the formula of 500 mM imidazole, 500 mM sodium chloride, 20 mM disodium hydrogen phosphate; all above reagents are commercially available.

[0143] Preferably, the exosome is selected from exosome from human serum, and/or exosome from human urine, and/or free exosome from other source, and/or exosome from cell culture supernatant.

[0144] The 9.sup.th group of examples: a method for purifying extracellular vesicle of the invention.

[0145] This group of embodiments provides a method for purifying extracellular vesicle, characterized in that, comprises binding or capturing the extracellular vesicle with the polypeptide EXP according to any of the 1.sup.st group of examples.

[0146] In further embodiments, the method for purifying microvesicles also includes:

[0147] Step 1: His labeled EXP and CP05 (100 μg) were combined with 40 μL nickel beads in 200 μL binding solution at 4° C. for 1 h under rotation.

[0148] Step 2: 1 mL of pre-centrifuged serum (4400 g, centrifugation for 20 min; 13000 g, centrifugation for 5 min) was added to the nickel beads coated with His-EXP and His-CP05, and was incubated at 4° C. for 30 min under rotation.

[0149] Step 3: discarding the serum and washing off non-specific binding with the washing buffer for 3 times (10 min each time).

[0150] Step 4: adding 100 μL of the elution buffer to recover the extracellular vesicle.

[0151] In some embodiments, the extracellular vesicle is selected from exosome and/or microvesicle.

[0152] The 10.sup.th group of examples: Use of the polypeptide EXP in pharmacy.

[0153] This group of embodiments provides use of said polypeptide EXP according to any of the 1.sup.st group of examples in pharmacy.

[0154] In specific embodiments, the use includes that said polypeptide EXP is connected with the drug delivery vector to obtain the enhanced drug delivery vector based on the polypeptide EXP-vector complex.

[0155] In further embodiments, said use also includes: the drug molecule is connected with the EXP-vector complex to obtain the drug based on the drugs molecule-EXP-vector complex.

[0156] In some further embodiments, said use also includes: targeting peptide is further connected with the drug molecule-EXP-vector complex to obtain targeted drug.

[0157] The 11.sup.th group of examples: use of the polypeptide EXP in manufacturing disease diagnostic reagent in the present invention

[0158] This group of embodiments provides use of the polypeptide EXP of any of the 1.sup.st group of examples in manufacturing disease diagnostic reagent.

[0159] In specific embodiments, the application includes: the polypeptide EXP is connected with the exosome.

[0160] In some embodiments, said exosome is derived from human serum, human urine, or other source.

Experimental Example 1: Flow Cytometry Assay was Used to Detect the Binding Capacity of EXP and Other Peptides to Exosome

[0161] 1.1 Flow Cytometry is Used to Detect the Binding Capacity of EXP and Other Peptides to Exosome.

[0162] (1) FAM-labeled CP05 and other peptides respectively with amount of 0.06 g were mixed with exosome from different source like dC2C12, CDC and serum respectively with amount of 10 μg, and DPBS is used to make up a deficiency to 200 μl in volume with.

[0163] (2) The mixture prepared as described in (1) was incubated at 4° C. for 2-4 hrs under rotation in vertical shaker.

[0164] (3) the binding efficiency was detected with flow cytometry.

[0165] The results were shown in FIG. 1(A).

[0166] 1.2 Detection on the Capacity Entering Cells of Exosome-Mediated CP05 and Other Peptides.

[0167] (1) C2C12 cells were digested, counted and seeded into 24-well plates (4×10.sup.4/well) and grown at 5% CO.sub.2 at 37° C. for 12 hrs.

[0168] (2) FAM-labeled CP05 and other peptides were incubated for 4 hrs as described in 1.1.

[0169] (3) the incubated EXO.sub.EXP and EXO.sub.CP05 were respectively added into C2C12 cells and incubated in serum-free DMEM medium for another 24 hrs by changing medium.

[0170] (4) Dead cells and fluorescent molecule non-specifically bound to the surface of cells were washed off with DPBS 24 hrs later.

[0171] (5) Cells were digested with 0.25% trypsin.

[0172] (6) centrifugation was performed at 1000 rpm for 5 min and the supernatant was discarded.

[0173] (7) Cell precipitates were re-suspended with 500 μlDPBS.

[0174] (8) centrifugation was performed at 1000 rpm for 5 min and the cell precipitates were washed twice.

[0175] (9) Cell precipitates were resuspended with 200 μl DPBS.

[0176] (10) the percentage of FITC-positive cells after adding EXO.sub.CP05 and EXO.sub.EXP was analyzed by Flow cytometry.

[0177] The results were shown in FIGS. 1(B) and (C).

Experimental Example 2: Detection of the Binding Stability of EXP and CP05 to Exosome

[0178] (1) C2C12 cells were digested, counted and seeded into 24-well plates (4×10.sup.4/well) and grown at 37° C. under 5% CO.sub.2 for 12 hrs.

[0179] (2) FAM-labeled EXP and CP05 (20 μg) were respectively incubated with DiI-labeled exosomes (10 μg) at 4° C. for 4 hrs under rotation.

[0180] (3) The incubated EXO.sub.EXP and EXO.sub.CP05 respectively were added into C2C12 cells and after changing medium, cells were cultured in serum-free DMEM medium at 37° C.

[0181] (4) after being cultured for different time (6 hrs, 12 hrs, 24 hrs, 48 hrs), cells were washed by DPBS.

[0182] (5) Cells were fixed with 4% paraformaldehyde at room temperature for 30 min, and were mounted.

[0183] (6) The co-localization efficiency of exosome (Dil) and polypeptide (FAM) and fluorescence energy transfer at different time-points were observed with confocal microscopy.

[0184] The results were shown in FIG. 2.

Experimental Example 3: Evaluation of Competitive Binding Capacity of Exosome Between EXP and CP05

[0185] (1) AF750-labeled CP05 (0.06 μg) was respectively incubated with FAM-labeled CP05 (0.06 μg, 0.3 μg) or FAM-labeled EXP (0.06 μg, 0.3 μg) and exosome (10 μg), and DPBS was used to make up a deficiency to 200 μl.

[0186] (2) Incubated for 4 hrs at 4° C. under rotation.

[0187] (3) Flow cytometry was used to examine the percentage of FITC- and APC-positive exosomes.

[0188] The results were shown in FIG. 3.

Experimental Example 4: Validation of EXP Target Detection

[0189] (1) 100 μg EXP or 100 μg CP05 were respectively mixed with 30 μl activated magnetic beads and incubated overnight at 4° C.

[0190] (2) The magnetic beads were recovered after washing off polypeptides that were unbound to magnetic beads with PBST.

[0191] (3) C2C12 cells were lysed with non-denatured tissue lysis buffer for 30 min on ice and centrifuged at 12000 rpm to recover supernatant.

[0192] (4) The supernatant of C2C12 lysis was added to the recovered magnetic beads and incubated for 2 hrs at 4° C.

[0193] (5) The supernatant was discarded and the precipitates were washed with PBST under rotation for 3 times (5 min each time) to wash off the nonspecific binding protein, and then PBST was discarded.

[0194] (6) 1× loading buffer (100 μl) was added into the precipitates and 50 μl sample was loaded into SDS-PAGE gels.

[0195] (7) The gels were stained with silver dyes or transferred to membrane and hybridized with CD63, CD9, CD81, CD82 antibodies.

[0196] The results were shown in FIG. 4.

Experimental Example 5: Comparison on Binding Efficiency of EXP and Exosomes from Different Sources

[0197] (1) 0.06 μg FAM-labeled CP05 and 0.06 μg of different peptides were respectively mixed with 10 μg exosome from dC2C12, CDC, serum, and DPBS was used to make up a deficiency to 200 μl.

[0198] (2) The mixture was incubated for 2-4 hrs at 4° C. under rotation in vertical shaker.

[0199] (3) The binding efficiency was detected with flow cytometry.

[0200] The results were shown in FIG. 5.

Experimental Example 6: Characterization and Functional Validation of Exosome Captured from Serum by EXP

[0201] (1) His-tagged EXP and CP05 (100 μg) were respectively mixed with 4 μl nickel beads in 200 μl binding solution at 4° C. for 1 h under rotation.

[0202] (2) 1 ml pre-centrifuged serum was added to His-EXP and His-CP05 coated nickel beads (centrifuged at 4400 g for 20 min, followed by 13000 g for 5 min), and then incubated at 4° C. for 30 min;

[0203] (3) The serum was discarded and the nonspecific binding was washed with the washing solution for 3 times, 10 min each time.

[0204] (4) 100 μl eluent was used to recover extracellular vesicles.

[0205] 6.1 Measurement of the Size of Captured Exosomes.

[0206] (1) 20 μl of exosomes recovered from elution were diluted into 1 ml of PBS.

[0207] (2) Nanosight was used to detect the size distribution of captured exosomes.

[0208] The results were shown in FIGS. 6(A) and (B).

[0209] 6.2 Morphological Identification of Captured Exosomes.

[0210] (1) 10 μl of recovered exosomes by elution and 10 μl of recovered exosomes by ultra-centrifugation were added with the same volume of 4% PFA for fixing.

[0211] (2) 10 μl exosomes fixing solution were absorbed onto the copper mesh for 20 min at room temperature.

[0212] (3) 100 μl PBS was dropped on the sealing membrane, with the copper mesh facing down, and unfixed exosomes on the copper mesh were washed off.

[0213] (4) For fixation, the copper mesh was transferred to 1% glutaraldehyde for 5 min.

[0214] (5) 100 μl H.sub.2O was dropped on the sealing membrane with the copper mesh facing down, and the copper mesh was washed for 8 times, 2 min each time.

[0215] (6) Transfer the copper mesh to 50 μl uranium oxalate solution (pH=7) and stain for 5 mm.

[0216] (7) the copper mesh was transferred to 50 μl methylcellulose-uranium oxalate on ice for 10 min.

[0217] (8) the copper mesh was taken out of methylcellulose-uranium oxalate and dried in air after drawing redundant liquid.

[0218] (9) the morphology of exosomes was observed with transmission electron microscopy.

[0219] The results were shown in FIG. 6C.

[0220] 6.3 Detection on Protein Expression of Captured Exosomes.

[0221] (1) 5 × loading buffer was added to 30 μl exosomes recovered by elution and 10 μg exosomes recovered by ultracentrifugation, and denatured at 100° C.

[0222] (2) The samples were loaded onto 10% SDS-PAGE and run for 1.5 hrs.

[0223] (3) protein transfer onto membrane at 250 mA for 2.5 hrs.

[0224] (4) the membrane was blocked for 2 hrs at 4° C.

[0225] (5) the primary antibodies (CD63, CD81, CD9, HSC90, Alix) were added and incubated overnight.

[0226] (6) the membrane was washed for 3 times with PBST, 10 min each time.

[0227] (7) the secondary antibody was incubated with the membrane for 2 hrs at 4° C.

[0228] (8) the membrane was washed with PBST for 3 times, 15 min each time.

[0229] (9) the membrane was developed.

[0230] The results were shown in FIG. 6(D).

Experimental Example 7: Exp Mediated the Functional Test of Exosomes Transporting PMO

[0231] 7.1 Immunohistochemical Staining of Muscle Tissues.

[0232] (1) anterior muscles (TA) of treated mdx mice was cut into 8-μm thick sections by freezing microtome;

[0233] (2) the sections was soaked in PBS for 15 min, blocking buffer containing 20% fetal bovine serum (FBS) and 20% goat serum (NGS) was added for blocking for 1 hour;

[0234] (3) the blocking buffer was discarded and dystrophin primary antibody (1:3000) was added for incubating for 2 hrs;

[0235] (4) the sections were washed with PBS for 3 times, and the fluorophore-labeled secondary antibody was added and incubated for 1 hr;

[0236] (5) the sections were washed with PBS for 3 times, mounted, dried in air and observed through the fluorescence microscope.

[0237] The results were shown in FIG. 7(A).

[0238] 7.2 Western Blot Staining

[0239] (1) 5× loading buffer was added to 50 μg different muscle samples and boiled at 72° C. for 5 min.

[0240] (2) the samples were loaded onto 4-6% SDS-PAGE gel and run for 2.5 hrs.

[0241] (3) proteins onto the membrane was transferred at 110 mA for 18 hrs.

[0242] (4) the membrane was blocked for 2 hrs at 4° C.

[0243] (5) the primary antibodies (dystrophin and α-actinin) was incubated with the membrane overnight.

[0244] (6) the membrane was washed with PBST for 3 times, 10 min each time.

[0245] (7) the membrane was incubated with secondary antibodies for 2 hrs at 4° C.

[0246] (8) the membrane was washed with PBST for 3 times, 15 min each time.

[0247] (9) the membrane was developed.

[0248] The results were shown in FIG. 7(C).

Example 8: Functional Evaluation on MV Mediated by EXP as Drug Delivery Vector

[0249] 8.1 The Procedures for MV Recovery.

[0250] (1) the cell supernatant or urine was balanced and centrifuged at 4500 g for 20 min at 4° C.

[0251] (2) the supernatant was collected with precipitate discarded and centrifuged at 13000 g for 5 min at 4° C.

[0252] (3) the supernatant was collected with precipitate discarded and centrifuged at 20000 g for 90 min at 4° C.

[0253] (4) the supernatant was discarded and the precipitate was resuspended with 1 ml PBS, and centrifuged at 20000 g for 90 min at 4° C.

[0254] (5) the supernatant was discarded and the precipitate was resuspended with 100 μl of PBS.

[0255] (6) Western Blot was used to detect the expression of biomarker protein, and nanosight was used to detect the size distribution of particles, their procedures were as above.

[0256] The results were shown in FIG. 8(A), 8(B).