Inside and outside of virus-like particles HBc and HBc/4M2e: A comprehensive study of the structure

Biophys Chem. 2023 Feb:293:106943. doi: 10.1016/j.bpc.2022.106943. Epub 2022 Dec 5.

Abstract

Hepatitis B virus core antigen (HBc) with the insertion of four external domains of the influenza A M2 protein (HBc/4M2e) form virus-like particles whose structure was studied using a combination of molecular modeling and cryo-electron microscopy (cryo-EM). It was also shown that self-assembling of the particles occurs inside bacterial cells, but despite the big inner volume of the core shell particle, purified HBc/4M2e contain an insignificant amount of bacterial proteins. It was shown that a fragment of the M2e corresponding to 4M2e insertion is prone to formation of amyloid-like fibrils. However, as the part of the immunodominant loop, M2e insertion does not show a tendency to intermolecular interaction. A full-atomic HBc-4M2e model with the resolution of about 3 Å (3.13 Å for particles of Т = 4 symmetry, 3.7 Å for particles of Т = 3 symmetry) was obtained by molecular modeling methods based on cryo-EM data.

Keywords: Cryo-electron microscopy; Hepatitis B virus core antigen; Influenza virus; Molecular modeling; Structural analysis; Virus-like particles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cryoelectron Microscopy
  • Hepatitis B Core Antigens* / chemistry
  • Hepatitis B virus / chemistry
  • Models, Molecular
  • Viral Matrix Proteins* / chemistry

Substances

  • Hepatitis B Core Antigens
  • M2 protein, Influenza A virus
  • Viral Matrix Proteins