Virus-mimetic nanovesicles as a versatile antigen-delivery system

Proc Natl Acad Sci U S A. 2015 Nov 10;112(45):E6129-38. doi: 10.1073/pnas.1505799112. Epub 2015 Oct 26.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens / metabolism*
  • Drug Delivery Systems / methods*
  • Nanostructures / chemistry*
  • Nanotechnology / methods
  • Nanotechnology / trends
  • Phospholipids / analysis
  • Recombinant Proteins / metabolism
  • Surface-Active Agents / analysis
  • Transport Vesicles / chemistry*
  • Viral Vaccines / metabolism*

Substances

  • Antigens
  • Phospholipids
  • Recombinant Proteins
  • Surface-Active Agents
  • Viral Vaccines