Patent Application
20090298955
The present invention relates to an altered virus capsid protein of SV40 and use thereof. According to the present invention, the cell tropism of a virus capsid protein, which can be expected to have potential applicability to gene therapy, drug delivery and the like, can be altered by biotechnological procedures. Since the virus capsid protein altered in such way has an ability to form a virus-like particle, particular genes, nucleic acids or pharmaceutically active substances can be encapsulated into the virus-like particle, and thus can be introduced into a particular cell, tissue or organ.
Conventional methods of gene transfection and drug delivery by virus vector and virus-like particles had depended on the efficient tropism of virus to the target cell, which is originally possessed by the virus particles. Therefore, the cell species in to which each biologically active substance was able to be introduced by such method were limited, depending on the cell or the organ tropism of the virus particles themselves. To overcome such limitations, development of technology to modify the cell tropism possessed by viruses themselves has long been studied especially with respect to non-enveloped viruses which are mostly composed of only proteins and nucleic acids, generally having stability and long term storage tolerance. As a method of this approach, insertion of a foreign peptide having high cell tropism into a capsid protein of virus can be assumed.
In addition, in mouse polyomavirus (Stubenrauch K, et al. Biochem J. 356:867-873; Shin YC, et al. J Virol., 77:11491-11498) and human papilloma virus (Slupetzky K, et al. J Gen Virol. 82:2799-804; Sadeyen J R, et al. Virology. 309:32-40), a peptide chain was inserted into each virus capsid protein using similar procedures, and particle formation by some of the capsid proteins having peptide insertion has been observed. However, there has been no report on examining presentation of an inserted peptide chain, particle-forming capability and cell tropism of an altered capsid protein simultaneously, and, the present study is the first time for this kind of study using SV40.
However, when alteration of amino acid sequence of the virus capsid protein was carried out by introducing foreign peptide into amino acid sequence of the virus capsid protein to alter the cell tropism of virus capsid protein, there had been such anxieties that most of the altered virus capsid protein lost particle-forming ability, or that desired characteristics of the altered capsid protein were not exerted because the introduced foreign peptide was not presented on the surface of the virus particle. Therefore, the present invention is directed to controlling specificity and efficiency of the introduction of a gene or a drug and the like to cells, by finding an appropriate insertion site for a foreign peptide in a capsid protein of a papovavirus which is infectious to primates, particularly of SV40 virus which can be expected to be highly safe to humans and have good structural stability, and then inserting the foreign peptide into the specified site, to control the cell tropism of the particles formed by the altered capsid protein.
To solve the above-described problems, the present inventors have searched for the insertion site so that the capsid protein can form a particle while the inserted peptide is presented, by inserting a foreign peptide into various regions (refer to
Thus, the present invention provides an altered capsid protein in which a foreign peptide sandwiched by 1 to several spacer amino acid residues is inserted into an amino acid residue constituting the surface of a capsid particle of a capsid protein of primate-infective papovavirus. The above-described primate-infective papovavirus includes, for example, SV40, JCB, BKV and the like. The above-described spacer amino acid residue includes, for example, glycine, serine, alanine, and the like.
More specifically, the present invention provides an altered capsid protein of SV40, in which a foreign peptide sandwiched by 1 to several glycine residues at each end is inserted into at least one of DE-loop and HI-loop of the capsid protein of SV40.
The capsid protein of SV40 is preferably SV40 VP1 capsid protein (SEQ ID NO: 13). The insertion site of the foreign peptide in the DE-loop is preferably positioned between the 127th and the 146th amino acids counted from the N-terminus of the SV40 VP1capsid protein, and the insertion site in the HI-loop is preferably positioned between the 268th and the 277th amino acids counted from the N-terminus of the SV40 VP1 capsid protein.
Further, another capsid protein, which can be used in the present invention, includes JCV (amino acid sequence is represented by SEQ ID NO: 13), BKV (amino acid sequence is represented by SEQ ID NO: 14), and the like. An expected possible insertion site of the foreign peptide into JCV is in between the 119th and 138th amino acids or in between the 260th and 269th amino acids counted from the N-terminus. Also, an expected possible insertion site of the foreign peptide into BKV is positioned between the 127th and 146th amino acids or positioned between the 268th and 277th amino acids counted from the N-terminus.
The number of glycine residues is preferably 1 to 6, for example, 3 to 6 for each side of the foreign peptide.
The foreign peptide includes, for example, Flag sequence (Asp-Tyr-Lys-Asp-Asp-Asp-Asp-Lys) (SEQ ID NO: 1), Myc sequence (Glu-Gln-Lys-Leu-Ile-Ser-Glu-Glu-Asp-Leu) (SEQ ID NO: 4), HA sequence (Tyr-Pro-Tyr-Asp-Val-Pro-Asp-Tyr-Ala) (SEQ ID NO: 5), Tat-PTD sequence (Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg) (SEQ ID NO: 6), polylysine sequence (3) (Lys-Lys-Lys) (SEQ ID NO: 7), polylysine sequence (6) (Lys-Lys-Lys-Lys-Lys-Lys) (SEQ ID NO: 8), polylysine sequence (12) (Lys-Lys-Lys-Lys-Lys-Lys-Lys-Lys-Lys-Lys-Lys-Lys) (SEQ ID NO: 9), NGR sequence (Gln-Gly-Arg) (SEQ ID NO: 10), 6×His sequence (His-His-His-His-His-His) (SEQ ID NO: 11) or polylysine sequence (8) (Lys-Lys-Lys-Lys-Lys-Lys-Lys-Lys) (SEQ ID NO: 12) or anantig enepitope. An example of the antigen epitope includes TAT-PTD sequence of human immune deficiency syndrome (HIV) (Tyr-Gly-Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg) (SEQ ID NO: 2) and amino acid sequence 3×RGD comprising integrin recognition sequence (RGD) (Arg-Gly-Asp-Arg-Gly-Asp-Arg-Gly-Asp) (SEQ ID NO: 3).
The present invention also provides a virus-like particle formed from the altered capsid protein of SV40 described above.
The present invention further provides the above-described virus-like particle, in which a biologically active substance is encapsulated. The biologically active substance is, for example, a pharmaceutically active ingredient or a nucleic acid for gene therapy.
Further, the present invention provides a pharmaceutical composition comprising the above-described virus particle.
In
When a pharmaceutically active ingredient or a nucleic acid for gene therapy is introduced into a subject using a virus, a point of concern is safety thereof. Many viruses used as an introduction vector are sometimes pathogenic by themselves, and a structural protein of a virus sometimes has cytotoxicity. On the other hand, many papovaviruses such as SV40 do not exert pathological change even when infecting the host. Especially, with respect to SV40, in the background of its discovery, the virus has been injected to humans in a large scale as a contaminating virus in polio vaccine, and as to the emergence of a pathological disorder caused by the injection of SV40, there has been none reported.
At the present time, as these viruses are considered to be harmless or to have a very low pathogenesis to humans, the capsid protein thereof may be expected to provide high safety in use for gene transfection, drug delivery, or the like into humans, if the cell tropism of the capsid protein of the virus can be controlled successfully. Therefore, in the present invention, a capsid protein of SV40, preferably the VP1 capsid protein of SV40 is utilized.
In the present invention, the insertion site of the foreign peptide is within the DE-loop or within the HI-loop of the capsid protein of SV40. In the case of the SV40 VP1 capsid protein, the DE-loop is located between the 127th and the 146th amino acids, and the HI-loop is located between the 268th and the 277th amino acids counted from the N-terminus of the protein. Preferably, the foreign peptide is inserted in between the 137th and 138th amino acid in the DE-loop, or in between the 272nd and 275th amino acid in the HI-loop of the SV40 VP1 capsid protein.
The foreign peptide to be inserted needs to have 1 to several spacer amino acids, for example, glycine, alanine or serine, and preferably 1 to 9 amino acids, more preferably 1 to 6 amino acids, for example 3 to 6 amino acids are present in each side of the peptide. If the peptide has no such spacer amino acid, formation of virus-like particles becomes difficult.
A preferable foreign peptide is a peptide that can change the cell tropism of a virus-like particle by inserting into the above-described insertion site, and includes Flag sequence (Asp-Tyr-Lys-Asp-Asp-Asp-Asp-Lys) (SEQ ID NO: 1), TAT-PTD sequence as an antigen epitope of human immune deficiency syndrome virus (HIV) (Tyr-Gly-Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg) (SEQ ID NO: 2) or amino acid sequence 3×RGD comprising integrin recognition sequence (RGD) (Arg-Gly-Asp-Arg-Gly-Asp-Arg-Gly-Asp) (SEQ ID NO: 3).
The foreign peptide further includes Myc sequence (Glu-Gln-Lys-Leu-Ile-Ser-Glu-Glu-Asp-Leu) (SEQ ID NO: 4), HA sequence (Tyr-Pro-Tyr-Asp-Val-Pro-Asp-Tyr-Ala) (SEQ ID NO: 5), 6×His sequence (His-His-His-His-His-His) (SEQ ID NO: 11), polylysine sequence (Lys-Lys-Lys-Lys-Lys-Lys-Lys-Lys) (SEQ ID NO: 12), Tat-PTD sequence (Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg) (SEQ ID NO: 6), polylysine sequence (3) (Lys-Lys-Lys) (SEQ ID NO: 7), polylysine sequence (6) (Lys-Lys-Lys-Lys-Lys-Lys) (SEQ ID NO: 8), polylysine sequence (12) (Lys-Lys-Lys-Lys-Lys-Lys-Lys-Lys-Lys-Lys-Lys-Lys) (SEQ ID NO: 9), NGR sequence (Gln-Gly-Arg) (SEQ ID NO: 10) and the like.
The present invention also relates to a virus-like particle formed from the above-described altered capsid protein. For the purpose of practical use, a biologically active substance, typically, a pharmaceutically active substance or a nucleic acid for gene therapy is encapsulated within the virus-like particle. The pharmaceutically active substance may be a compound having a low molecular weight, particularly an organic compound having a low molecular weight, or a compound having a high molecular weight such as polypeptides, protein or polysaccharides. Examples of such substances include anti-tumor agents such as adriamycin, cyclophosphamide, proteins having anti-tumor activity such as TNFα, Granzyme B, and the like.
In addition, a gene (a nucleic acid) for gene therapy is not particularly limited, and includes, for example, human normal genes such as adenosine deamidase gene, p53 gene, and the like; DNA which can express siRNA and suppress specific gene expression by RNA interference; siRNA itself, and the like.
The present invention will be explained more specifically by the Examples.
In this Example, focusing on 3 domains, the BC-loop, the HI-loop and the DE-loop, among domains presented at the outside of SV40 (see
In the next, Sf9 cells seeded in tissue culture dishes (IWAKI) having a diameter of 10 cm in the population of 1×107 cells per dish were infected with recombinant baculoviruses at an m.o.i. (Multiplicity of Infection) of 5 to 10, which can express each of altered type virus protein (VP1) of SV40. The recombinant baculoviruses, which can express each of altered type VP1proteins, were prepared using Bac-to-Bac Baculovirus Expression System produced by Invitrogen Corp.
At 72 hours after the infection by the recombinant baculoviruses, Sf-9 cells were recovered and washed twice with cooled phosphate buffered saline (PBS) . The recovered cells were suspended in 200 μl of ice-cooled buffer for sonication (20 mM Tris-HCl (pH 7.9), 1% (w/v) sodium deoxycholate (DOC), 2 mM PMSF, 1 μg/ml chymostatin, aprotinin, leupeptin, antipain, pepstatin), then disrupted by ultrasonication under ice-cooling for 20 seconds, followed by standing on ice bath for 20 seconds. After repeating this procedure 3 times, the disruption mixture was centrifuged under 15,000×g at 4° C. for 10 minutes to recover supernatant solution. Two μl of the recovered VP1 protein was subjected to Western blot analysis using anti-VP1 antibody to determine its expression (
After determination of the expression, 2 μl of the cell disruption mixture was diluted by 10 times over to 20 μl with 20 mM Tris-HCl (pH 7.9), and then fractionated by 20 to 40% (w/v) sucrose density-gradient centrifugation (at 55,000 rpm, at 4° C. for 1 hour) using Open Top Ultraclear Tube for SW51Ti (Beckman).
Samples of fractions obtained from 20 to 40% (w/v) sucrose density-gradient centrifugation were analyzed for VLP forming capability of the altered VP1 by Western blotting using anti-VP1 antibody. Peak of VP1-VLP formed by wild type VP1 protein (hereinafter, referred to as Wt-VLP) was detected in 8th through 10th fractions (
Two hundreds micro litter of the cell disruption mixture was fractionated by 20 to 50% (w/v) cesium chloride density-gradient centrifugation (at 35,000 rpm, at 4° C. for 3 hours) using Open Top Ultraclear Tube for SW51Ti (Beckman). After ultracentrifugation, 5 μl each of fractionated samples were transferred and adsorbed on a copper mesh coated with carbon collodion membrane, followed by washing with pure water, then stained using 2 to 6% uranium acetate solution and dried. Observation was carried out using a HITACHI H-7500 Electron Microscope. It was confirmed that the altered type VP1 having Flag sequence insertion in DE-loop or HI-loop formed virus-like particles with almost the same shape and size as that formed from Wt-VLP. The results of analysis on the virus-like particle-forming capability of altered type VP1 were summarized in the following Table 1 (
In this Example, what effect the number of glycine residues to be added to each side of a Flag sequence inserted into the loop domain has on the formation of virus-like particles of the altered type VP1 was studied.
Using HI-loop of the above-described loop domains as a target site, altered type VP1 genes inserted with Flag sequence having 0 to 6 glycine residues in each side thereof were prepared according to the same procedures as described in Examples 1 and 2. The results are shown in
In addition, from the results of Western blotting analysis of the samples fractionated by sucrose density-gradient centrifugation using anti-VP1 antibody, it was found that efficiency of the formation of virus-like particles of the sample added with 3 glycine residues was better than the sample added with 1 or 2 residues. From the above findings, it was shown that for the formation of virus-like particles by the altered type VP1 inserted with Flag sequence, glysine residue is necessary as a spacer for both sides thereof, and that the number is preferably at least 3 residues.
To determine whether the Flag sequence inserted as an epitope into the altered type VP1 actually works as an epitope, immunoprecipitation was carried out using an anti-Flag antibody. Twenty μl of altered type virus-like particle (altered type VLP) prepared by the same method as described in the last paragraph of Example 2 was added with phosphate buffered saline (PBS) to give 100 μl, and then agitated gently at 4 C. for 1 hour together with 50 μl of anti-Flag M2 Affinity Gel (Sigma). After agitation, the gel was washed twice with 250 μl of phosphate buffered saline (PBS), and then eluted using 1 μg/μl of Flag peptide. The eluate sample was subjected to Western blotting using anti-VP1 antibody. By this experiment, it was confirmed that only the altered type VLP having insertion of Flag sequence in the DE-loop and the altered type VLP having insertion of Flag sequence in the HI-loop could bind to anti-Flag antibody (
Analysis of the Function of Flag Sequence in the Virus-Like Particle Formed from Altered Type VP1
To determine whether the inserted Flag sequence still retains function as an epitope in the altered type VLP after the VLP is formed, the following experiment was carried out. Altered type VLPs of 60 ng each were prepared according to the same procedures as described in Example 1 and Example 2, and each of altered type VLPs was mixed with 9 μg of anti-Flag antibody (Sigma) and anti-His antibody (Sigma) , respectively, and agitated gently at 4° C. for 1 hour. After agitation, each mixture was fractionated by 20 to 40% (w/v) sucrose density-gradient centrifugation, followed by Western blotting. When anti-Flag antibody was used, both VP1 and anti-Flag antibody were detected at the peak fractions of fraction number 9 and 10. On the other hand, when anti-His antibody was used, only VP1 was detected at the peak fraction (
To prepare a large amount of altered type virus-like particles, Sf9 cells seeded in 10 tissue culture dishes (IWAKI) with a diameter of 15 cm with a population of 3×107 cells per dish were infected with each of recombinant baculoviruses, which expresses each altered type virus protein (VP1) of SV40, at an m.o.i. (Multiplicity of Infection) of 5 to 10.
At 72 hours after the recombinant baculovirus infection, Sf-9 cells were recovered and washed twice with cooled phosphate buffered saline (PBS). The recovered cells were suspended in 10 ml of ice-cooled buffer for sonication (20 mM Tris-HCl (pH 7.9), 1% (w/v) sodium deoxycholate (DOC), 2 mM PMSF, 1 μg/ml chymostatin, aprotinin, leupeptin, antipain, pepstatin), then disrupted by ultrasonication under ice-cooling for 10 minutes. After repeating this procedure twice, the cell disruption mixture was centrifuged under 15,000×g at 4° C. for 10 minutes to recover the supernatant solution.
In an Open Top Ultraclear Tube for SW41Ti (Beckman), 1.5 ml each of cesium chloride solutions with different densities (50%, 40%, 30%, 20% (w/v)) were overlaid in the order of decreasing density, then 5 ml of the above-described cell disruption mixture was overlaid on the top of the cesium chloride layers. After that, the tube was centrifuged using SW41Ti rotor at 30,000 rpm, at 4° C. for 3 hours. The white layer of virus-like particles of SV40 formed in the midpoint of the density gradient was recovered and diluted with 37% (w/v) cesium chloride solution. Thereafter, the diluted solution was transferred to an Open Top Ultraclear Tube for SW55Ti and centrifuged at 50,000 rpm using SW55Ti rotor at 4° C. for 20 hours, and the layer of virus-like particles formed again was recovered.
For the purpose of studying the effects of each inserted motif on the processes of adsorption and internalization of the altered type virus-like particles (Flag virus-like particles, 3×RGD virus-like particles, and TAT-PTD virus-like particles) into the cells, the following experiments were carried out.
HeLa cells (human uterine cervix cancer cells) were seeded in a tissue culture dish (IWAKI) with a diameter of 10 cm in a population of 1×106 cells per dish. Also, the wild type virus-like particles and the altered type virus-like particles prepared in Example 7 were diluted with phosphate buffered saline (PBS) to give the concentrations of 4×104, 4×105, and 4×106 particles per cell.
Each of the wild type virus-like particles and the altered type virus-like particles (4×104, 4×105, and 4×106 VLPs/cell) prepared as described above was added with culture medium (DMEM+10% FBS) to make 1 ml each, and inoculated on the above described HeLa cells, followed by rocking every 15 minutes at room temperature. After 4 times of rocking, 9 ml each of culture medium was added and incubated at 37° C. for 1 hour. Thereafter, the samples were recovered and washed twice with phosphate buffered saline (PBS). The HeLa cells were recovered by two different methods in accordance with the intended use.
To detect both of the virus-like particles adhered on the surface of HeLa cells and the virus-like particles internalized into the cells, HeLa cells were recovered using a scraper (IWAKI).
For the purpose of detecting only internalized virus-like particles, 1 ml of 0.25% Trypsin-EDTA (Gibco) was added to each tissue culture dish with a diameter of 10 cm, and the cells were incubated at 37° C. for 5 minutes, then cells detached from the dishes were recovered.
The cells recovered by the above-described method were washed twice with phosphate buffered saline (PBS), and suspended in 200 μl of ice-cooled buffer for sonication, then disrupted by ultrasonication for 60 seconds. The disruption mixture was subjected to Western blotting analysis using anti-VP1 antibody to detect the VP1 proteins both adsorbed on and internalized into the HeLa cells. The results are shown in Table 3.
Also, the results are shown in
A shows the electron microscopic pictures of particles consisted of virus capsid protein in which TAT-PTD or 3×RGD amino acid sequence was inserted into HI-loop thereof. Each particle was almost spherical with a diameter of about 50 nm, and had seemingly no difference from the wild type particle (not shown herein) . The black bars at the bottoms indicate 100 nm in length.
Wild type particles and particles consisted of virus capsid protein, in which Flag, 3×RGD or TAT-PTD amino acid sequence was inserted, were each infected to CV-1 cells; after standing for 1 hour cells were recovered, then an amount of internalized particles (an amount of VP1) was detected by Western blotting (B and C). By varying the amount of particles infected as shown by “Input”, comparison of the amounts of VP1 detected in the cells was tried. “Cell associated” means that the infected cells were recovered without using proteolytic enzymes such as trypsin, and detection of the particles of both adsorbed on the cell surface and internalized into the cells was tried. “Internalized” means that recovery of the infected cells was carried out by trypsin treatment, for the purpose of quantitatively determining only the particles (VP1) remaining in the cells by digesting the particles adsorbed on the surface of the cell.
As seen in B and C, Wt particles were able to adsorb on the cells (see Cell associated) and also intrude into the cells (see Internalized), while it was observed that the Flag-inserted particles were inhibited at the adsorption step (B). Also, 3×RGD-inserted particles were able to adsorb on the cell similarly to Wt, but internalization thereof was inefficient (C). On the other hand, it was clearly demonstrated that the TAT-PTD-inserted particles were able to intrude into the cells similarly to the Wt particles (C)
These results indicate that introduction of a peptide chain itself leads to losing the cell tropism of original capsid protein, and also a new cell tropism can be acquired by introducing such a peptide chain as TAT-PTD.
Wild type particles (Wt) or particles consisted of virus protein in which Flag (Flag-DE2) or TAT-PTD (Tat-PTD-DE2) amino acids have been inserted into DE-loop were each infected to HeLa cells, and after 2 hour cells were recovered, then the amount of internalized particles (an amount of VP1) was detected by Western blotting. In the recovery of the cells, the particles adsorbed on the surface of the cells were degraded by trypsin, and only the particles internalized into the cells were detected. As shown by “Input”, almost the same amount of particles were used for the introduction into the cells. As shown by “Internalized”, the amount of VP1 detected in the cells was almost nothing for Flag-DE2, and slightly lower but comparable for TAT-PTD-DE2 as compared to that for Wt. These results indicate that, as observed similarly when a peptide chain is inserted into HI-loop, introduction of a peptide chain into DE-loop itself leads to losing the cell tropism of original capsid protein, and a new cell tropism can be acquired by introducing such a peptide chain as TAT-PTD (
Analysis of the function of altered type virus-like particle (2)
The experiment described in Example 8 was repeated. In this regard, however, instead of the method using trypsin, observation by a confocal microscope was carried out. Flag-HI1 having an insertion of the Flag sequence in the HI-loop, 3×RGD-HI1 having an insertion of the 3×RGD sequence (RGD-RGD-RGD) in the HI-loop, Flag-DE2 having an insertion of the Flag sequence in the DE-loop and 3×RGD-DE2 having an insertion of the 3×RGD sequence (RGD-RGD-RGD) in the DE-loop, and wild type VLP (Wt) were tested. The results of detection using anti-VP1 antibody and observation using a confocal microscope are shown in
In
As the results of the above-described experiment, 3×RGD-HI1 and 3×RGD-DE2 having an insertion of the 3×RGD sequence (RGD-RGD-RGD) in the HI-loop or the DE-loop were endocytosed by the cells at the same level as observed for wild type VLP. The results are summarized in Table 3.
TAT-PTD sequence of human immune deficiency syndrome virus (HIV) (Tyr-Gly-Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg) (SEQ ID NO: 2) or amino acid sequence 3×RGD comprising integrin recognition sequence (RGD) (Arg-Gly-Asp-Arg-Gly-Asp-Arg-Gly-Asp) (SEQ ID NO: 3), or Flag sequence (Asp-Tyr-Lys-Asp-Asp-Asp-Asp-Lys) (SEQ ID NO: 1) and the like were introduced into the surface loops, specifically between the 136th and 139th or between the 272nd and 275th amino acids of the VP1 amino acid sequence of SV40 capsid protein, and then particles were formed with these altered type VP1s. The altered type VP1s were able to form particles regardless of the amino acid sequence introduced.
In addition, the inserted amino acid sequences were able to be recognized by antibody without denaturing the altered type VP1, and therefore, those sequences were presented on the surface of the particles. Using such particles, introduction into CV-1 cells or HeLa cells was tested. As the results, the Flag-inserted altered type particles were mostly unable to adsorb to the cells. On the other hand, the particles inserted with 3×RGD were able to adsorb to the cells, but the internalization efficiency thereof was lower compared to that of the wild type. However, the particles inserted with TAT-PTD sequence were able to adsorb to the cells and internalized, and efficiency thereof was slightly higher than that of the particles comprising wild type VP1. Namely, it is indicated that the cell tropism originally possessed by the virus capsid protein is inactivated by insertion of a peptide chain, but a new cell tropism is provided by the function of inserted peptide chain.
By the insertion of a foreign peptide chain into the right position of a virus capsid protein, efficient presentation of the peptide chain could be achieved without inhibiting particle formation of the capsid protein. By this insertion of a peptide chain, the cell tropism originally possessed by the virus capsid protein was inhibited, and the cell tropism of the particle could be controlled with the inserted peptide chain.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2005-039102 | Feb 2005 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2006/303209 | 2/16/2006 | WO | 00 | 12/9/2008 |
