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Severe acute respiratory syndrome coronavirus protein 7a interacts with hSGT

  • Burtram C. Fielding
  • , Vithiagaran Gunalan
  • , Timothy H.P. Tan
  • , Chih Fong Chou
  • , Shuo Shen
  • , Sehaam Khan
  • , Seng Gee Lim
  • , Wanjin Hong
  • , Yee Joo Tan
  • Agency for Science, Technology and Research, Singapore
  • University of the Western Cape

Research output: Contribution to journalArticlepeer-review

35 Citations (Scopus)

Abstract

Severe acute respiratory syndrome coronavirus (SARS-CoV) 7a is an accessory protein with no known homologues. In this study, we report the interaction of a SARS-CoV 7a and small glutamine-rich tetratricopeptide repeat-containing protein (SGT). SARS-CoV 7a and human SGT interaction was identified using a two-hybrid system screen and confirmed with interaction screens in cell culture and cellular co-localization studies. The SGT domain of interaction was mapped by deletion mutant analysis and results indicated that tetratricopeptide repeat 2 (aa 125-158) was essential for interaction. We also showed that 7a interacted with SARS-CoV structural proteins M (membrane) and E (envelope), which have been shown to be essential for virus-like particle formation. Taken together, our results coupled with data from studies of the interaction between SGT and HIV-1 vpu indicated that SGT could be involved in the life-cycle, possibly assembly of SARS-CoV.

Original languageEnglish
Pages (from-to)1201-1208
Number of pages8
JournalBiochemical and Biophysical Research Communications
Volume343
Issue number4
DOIs
Publication statusPublished - 19 May 2006
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Accessory protein
  • ORF 7a
  • Protein-protein interaction
  • SARS-CoV
  • SGT
  • TPR

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Molecular Biology
  • Cell Biology

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