| Literature DB >> 26504197 |
Pengfei Zhang1, Yixin Chen2, Yun Zeng3, Chenguang Shen4, Rui Li4, Zhide Guo1, Shaowei Li5, Qingbing Zheng4, Chengchao Chu1, Zhantong Wang6, Zizheng Zheng4, Rui Tian1, Shengxiang Ge4, Xianzhong Zhang1, Ning-Shao Xia5, Gang Liu7, Xiaoyuan Chen8.
Abstract
It is a critically important challenge to rapidly design effective vaccines to reduce the morbidity and mortality of unexpected pandemics. Inspired from the way that most enveloped viruses hijack a host cell membrane and subsequently release by a budding process that requires cell membrane scission, we genetically engineered viral antigen to harbor into cell membrane, then form uniform spherical virus-mimetic nanovesicles (VMVs) that resemble natural virus in size, shape, and specific immunogenicity with the help of surfactants. Incubation of major cell membrane vesicles with surfactants generates a large amount of nano-sized uniform VMVs displaying the native conformational epitopes. With the diverse display of epitopes and viral envelope glycoproteins that can be functionally anchored onto VMVs, we demonstrate VMVs to be straightforward, robust and tunable nanobiotechnology platforms for fabricating antigen delivery systems against a wide range of enveloped viruses.Keywords: antigen delivery system; cell membrane; nanobiotechnology; vaccine; virus-mimetic vesicle
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Year: 2015 PMID: 26504197 PMCID: PMC4653155 DOI: 10.1073/pnas.1505799112
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205