In vitro method for disassmbly/reassembly of papillomavirus virus-like particles (VLPs). Homogeneous VLP and cavsomere compositions produced by said methods: use thereof as vehicle for improved purification, and delivery of active agents
A method of disassembly/reassembly of papillomavinis VLPs is provided. The resultant VLPs have enhanced homogeneity, present conformational, neutralizing PV epitopes, and therefore are useful prophylactic and diagnostic agents. Further, these VLPs can be used to encapsulate desired moieties, e.g., therapeutic or diagnostic agents, or marker” DNAs, and the resultant VLPs used as in vivo delivery vehicles or as pseudovirions for evaluating vaccine efficacy.
1. A method of producing purified human papillomavirus (HPV) virus-like particles (VLPs) comprising:
purifying a recombinantly expressed HPV L1 protein or truncated version thereof in the presence of at least one reducing agent that maintains said recombinantly expressed HPV L1 protein or truncated version thereof in a form other than a VLP; and
assembling said recombinantly expressed HPV L1 protein or truncated version thereof into purified human papillomavirus virus-like particles (VLPs).
2. The method of claim 1 wherein said human papillomavirus VLPs are selected from the group consisting of HPV-6, HPV-11, HPV-16, HPV-18, HPV-30, HPV-31, HPV-33, HPV-35, HPV-39, HPV-41, HPV-42, HPV-43, HPV-44, HPV-45, HPV-52, HPV-54, HPV-55, HPV-56, HPV-58, HPV-70, and mixtures thereof.
3. The method of claim 2 wherein said human papillomavirus VLP is an HPV-16 VLP.
4. The method of claim 2 wherein said human papillomavirus VLPs are HPV-16 VLPs and HPV-18 VLPs.
5. The method of claim 2 wherein said human papillomavirus VLP is an HPV-11 VLP.
6. The method of claim 1 wherein said reducing agent is a sulfhydryl reducing agent.
7. The method of claim 6 wherein said sulfhydryl reducing agent is β-mercaptoethanol.
8. The method of claim 1 wherein assembly of said HPV L1 protein or truncated version thereof is induced by oxidation or removal of said reducing agent.
9. A method of producing purified human papillomavirus (HPV) virus-like particles (VLPs), comprising:
purifying a recombinantly expressed HPV L1 protein or truncated version thereof in the presence of at least one reducing agent that maintains said recombinantly expressed HPV L1 protein or truncated version thereof in a form other than a VLP; and
assembling said recombinantly expressed HPV L1 protein or truncated version thereof into purified human papillomavirus virus-like particles (VLPs) by removing or oxidizing said at least one reducing agent.
10. The method of claim 9 wherein said human papillomavirus VLPs are selected from the group consisting of HPV-6, HPV-11, HPV-16, HPV-18, HPV-30, HPV-31, HPV-33, HPV-35, HPV-39, HPV-41, HPV-42, HPV-43, HPV-44, HPV-45, HPV-52, HPV-54, HPV-55, HPV-56, HPV-58, HPV-70, and mixtures thereof.
11. The method of claim 10 wherein said human papillomavirus VLP is an HPV-16 VLP.
12. The method of claim 10 wherein said human papillomavirus VLPs are HPV-16 VLPs and HPV-18 VLPs.
13. The method of claim 10 wherein said human papillomavirus VLP is an HPV-11 VLP.
14. The method of claim 9 wherein said reducing agent is a sulfhydryl reducing agent.
15. The method of claim 14 wherein said sulfhydryl reducing agent is β-mercaptoethanol.