Peptide domain involved in the interaction between membrane protein and nucleocapsid protein of SARS-associated coronavirus

J Biochem Mol Biol. 2005 Jul 31;38(4):381-5. doi: 10.5483/bmbrep.2005.38.4.381.

Abstract

Severe acute respiratory syndrome (SARS) is an emerging infectious disease associated with a novel coronavirus (CoV) that was identified and molecularly characterized in 2003. Previous studies on various coronaviruses indicate that protein-protein interactions amongst various coronavirus proteins are critical for viral assembly and morphogenesis. It is necessary to elucidate the molecular mechanism of SARS-CoV replication and rationalize the anti-SARS therapeutic intervention. In this study, we employed an in vitro GST pull-down assay to investigate the interaction between the membrane (M) and the nucleocapsid (N) proteins. Our results show that the interaction between the M and N proteins does take place in vitro. Moreover, we provide an evidence that 12 amino acids domain (194-205) in the M protein is responsible for binding to N protein. Our work will help shed light on the molecular mechanism of the virus assembly and provide valuable information pertaining to rationalization of future anti-viral strategies.

MeSH terms

  • Amino Acid Sequence
  • Coronavirus M Proteins
  • Coronavirus Nucleocapsid Proteins
  • Glutathione Transferase / genetics
  • Glutathione Transferase / metabolism
  • Membrane Fusion / physiology*
  • Molecular Sequence Data
  • Nucleocapsid Proteins / metabolism*
  • Protein Binding
  • Protein Interaction Mapping
  • Protein Structure, Tertiary
  • Recombinant Proteins / genetics
  • Recombinant Proteins / isolation & purification
  • Recombinant Proteins / metabolism*
  • Sequence Homology, Amino Acid
  • Severe acute respiratory syndrome-related coronavirus / metabolism*
  • Viral Matrix Proteins / metabolism*
  • Virus Assembly*

Substances

  • Coronavirus M Proteins
  • Coronavirus Nucleocapsid Proteins
  • M protein, SARS-CoV
  • Nucleocapsid Proteins
  • Recombinant Proteins
  • Viral Matrix Proteins
  • Glutathione Transferase