Characterization of the Lassa virus matrix protein Z: electron microscopic study of virus-like particles and interaction with the nucleoprotein (NP)

Virus Res. 2004 Mar 15;100(2):249-55. doi: 10.1016/j.virusres.2003.11.017.

Abstract

Lassa virus is the causative agent of a hemorrhagic fever endemic in west Africa. The RNA genome of Lassa virus encodes the glycoprotein precursor GP-C, a nucleoprotein (NP), the viral polymerase L and a small protein Z (11 kDa). Here, we analyze the role of Z protein for virus maturation. We have recently shown that expression of Z protein in the absence of other viral proteins is sufficient for the release of enveloped Z-containing particles. In this study, we examined particles secreted into the supernatant of a stably Z protein-expressing CHO cell line by electron microscopy. The observed Z-induced virus-like particles did not significantly differ in their morphology and size from Lassa virus particles. Mutation of two proline-rich domains within Z which are known to drastically reduce the release of virus-like particles, had no effect on the cellular localization of the protein nor on its membrane-association. Furthermore, we present evidence that Z interacts with the NP. We assume that Z recruits NP to cellular membranes where virus assembly takes place. We conclude from our data that Lassa virus Z protein plays an essential role in Lassa virus maturation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Amino Acid Substitution
  • Arenavirus / genetics
  • Binding Sites
  • Carrier Proteins / genetics*
  • Carrier Proteins / metabolism
  • Carrier Proteins / ultrastructure*
  • Genome, Viral
  • Lassa virus / genetics
  • Lassa virus / ultrastructure*
  • Molecular Sequence Data
  • Mutation
  • Nucleoproteins / metabolism*
  • Nucleoproteins / ultrastructure
  • RNA, Viral / genetics
  • RNA-Binding Proteins
  • Sequence Alignment
  • Sequence Deletion
  • Sequence Homology, Amino Acid
  • Viral Matrix Proteins / genetics*
  • Viral Matrix Proteins / metabolism
  • Viral Matrix Proteins / ultrastructure*

Substances

  • Carrier Proteins
  • Nucleoproteins
  • RNA, Viral
  • RNA-Binding Proteins
  • Viral Matrix Proteins
  • protein Z, Lassa virus