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Human papilloma virus L1L2 capsid protein interaction site and applications thereof

A technology of L1 protein and site, applied in the field of molecular virology, can solve problems such as limited application value and lack of experimental data

Active Publication Date: 2014-12-24
XIAMEN UNIV +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, these studies lack the support of experimental data, and the described areas of action of L1 and L2 are too broad, and the application value is limited

Method used

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  • Human papilloma virus L1L2 capsid protein interaction site and applications thereof
  • Human papilloma virus L1L2 capsid protein interaction site and applications thereof
  • Human papilloma virus L1L2 capsid protein interaction site and applications thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0058] Embodiment 1: Computer analysis predicts the interaction site of HPV16L1 and HPV16L2

[0059] The Discovery Studio software used for protein structure analysis and simulation in this laboratory was purchased from Accelrys, USA. Discovery Studio software was used to analyze the surface amino acids of HPVL1 pentamer that might interact with L2, and the amino acid solvent accessibility surfaces (solvent accessibility surfaces, SAS) were evaluated. SAS represents the ratio of the surface area of ​​the amino acid that can be exposed to the solvent to the surface area of ​​the entire amino acid, which is an index that reflects the degree of exposure of the amino acid. The larger the value, the higher the degree of exposure of the amino acid to the surface of the protein structure (Le Grand, S.M., Eyrand, V .An algorithm for the representation and computatio of suermolecular surface and volumes. J.Comp.Chen.1989,10:868-871). Among them, 23 sites were screened out, and their...

Embodiment 2

[0064] Embodiment 2: Construction of 23 pAAV-16L1 site mutation plasmids

[0065]Gene cloning is carried out by site-directed mutagenesis PCR reaction, using the pAAV-HPV16L1 plasmid constructed in this laboratory (gifted by Professor John T. Schiller of NIH, wherein the DNA sequence of HPV16L1 is as SEQ NO: 25 of the present invention) as a template (abbreviated as H16L1), the primers and products of each PCR reaction are shown in Table 2, use the primers designed in Table 3 to carry out PCR amplification, and perform PCR reaction in PCR instrument (Biometra, T3), and the amplification conditions are set as:

[0066] Denaturation at 94°C for 10 minutes, 25 cycles (denaturation at 94°C for 50 seconds, annealing at a specified temperature for a certain time, extension at 72°C for 6 minutes), and finally extension at 72°C for 10 minutes.

[0067] The amplified product was added with 2 μL DpnI restriction endonuclease, treated at 37° C. for 60 minutes, and then transformed into...

Embodiment 3

[0077] Embodiment 3: preparation of 23 HPV16 mutant pseudoviruses

[0078] The wild-type pAAV-16L1 plasmid obtained in Example 2 or 23 mutant pAAV-16L1 plasmids and pAAV-HPV16L2 plasmids (gifted by Professor John T. Schiller of NIH; those skilled in the art can construct by themselves, respectively) using calcium phosphate transfection method Other blank plasmids can also be used for enzyme digestion and recombination) and the plasmid pcDNA3.1-EGFP containing the reporter gene (for the construction method, see Lu Wuxun et al., Acta Biological Engineering, 2006, volume 22: 990-995) each with a total of 40 μg 293FT cells (purchased from Invitrogen) cultured in a 10 cm cell culture dish were transfected to prepare pseudoviruses or mutated pseudoviruses. Regarding the preparation of pseudoviruses, refer to Lu Wuxun et al., Acta Biological Engineering, 2006, volume 22: pages 990-995, and also refer to the following steps:

[0079] Add 40 μg each of the wild-type or mutant pAAV-1...

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Abstract

The invention belongs to the field of molecular virology, and particularly relates to a binding site of interacting a major capsid protein L1 and a secondary capsid protein L2 of a human papilloma virus L1L2. The protein binding site and an area can serve as target sites for preventing HPV infection and diseases such as a cervical cancer caused HPV infection. The invention further relates to an HPV mutant type L1 protein. The invention further relates to a medicament composition and applications of the preparation medicament composition in treating and / preventing and / adjuvantly treating HPV infection and diseases such as a cervical cancer caused by HPV infection.

Description

technical field [0001] The present invention relates to the field of molecular virology. In particular, the present invention relates to the binding site where the human papillomavirus major capsid protein L1 interacts with the minor capsid protein L2. The protein binding site can be used as a target site for preventing HPV infection and diseases caused by HPV infection, such as cervical cancer. The present invention also relates to HPV mutant L1 protein. The present invention also relates to a pharmaceutical composition and the use of the pharmaceutical composition for treating and / preventing and / assistingly treating HPV infection or diseases caused by HPV infection, such as cervical cancer. Background technique [0002] Human papillomavirus (Human Papillomavirus, HPV) belongs to the family Papillomaviridae (Papillomaviridae) papillomavirus genus, is a non-enveloped DNA virus. The virus genome is a double-stranded closed-circle DNA with a size of about 7.2-8kb and 8 open...

Claims

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Application Information

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IPC IPC(8): C07K14/025C12N15/37C12N15/70C12N15/85C12N1/21C07K19/00C12N7/00C12N7/04A61K39/12A61K48/00A61P31/20A61P35/00G01N33/68C12R1/93
CPCC07K14/005C07K2319/00C12N2710/20022C12N2710/20023C12N2710/22034G01N33/68G01N2800/7028
Inventor 李少伟吴坤宝张丽刘亚静王大宁俞海张军夏宁邵
Owner XIAMEN UNIV
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