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Interactions of SARS Coronavirus Nucleocapsid Protein with the host cell proteasome subunit p42

Supporting Files Public Domain


Details

  • Alternative Title:
    Virol J
  • Personal Author:
  • Description:
    Background

    Severe acute respiratory syndrome-associated coronavirus (SARS-CoV) spreads rapidly and has a high case-mortality rate. The nucleocapsid protein (NP) of SARS-CoV may be critical for pathogenicity. This study sought to discover the host proteins that interact with SARS-CoV NP.

    Results

    Using surface plasmon resonance biomolecular interaction analysis (SPR/BIA) and matrix-assisted laser desorption/ionization time of flight (MALDI-TOF) mass spectrometry, we found that only the proteasome subunit p42 from human fetal lung diploid fibroblast (2BS) cells bound to SARS-CoV NP. This interaction was confirmed by the glutathione S-transferase (GST) fusion protein pulldown technique. The co-localization signal of SARS-CoV NP and proteasome subunit p42 in 2BS cells was detected using indirect immunofluorescence and confocal microscopy. p42 is a subunit of the 26S proteasome; this large, multi-protein complex is a component of the ubiquitin-proteasome pathway, which is involved in a variety of basic cellular processes and inflammatory responses.

    Conclusion

    To our knowledge, this is the first report that SARS-CoV NP interacts with the proteasome subunit p42 within host cells. These data enhance our understanding of the molecular mechanisms of SARS-CoV pathogenicity and the means by which SARS-CoV interacts with host cells.

  • Subjects:
  • Source:
    Virol J. 2010; 7:99.
  • Document Type:
  • Volume:
    7
  • Collection(s):
  • Main Document Checksum:
    urn:sha256:403a781bf845584bfe421cc3bbca7a6185645ab41483292771d684db2702661f
  • Download URL:
  • File Type:
    Filetype[PDF - 771.54 KB ]
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