4.6 Article

Severe acute respiratory syndrome coronavirus 7a accessory protein is a viral structural protein

Journal

JOURNAL OF VIROLOGY
Volume 80, Issue 15, Pages 7287-7294

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.00414-06

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Funding

  1. NIAID NIH HHS [R01 AI029984, AI 29984, R21 AI029984, N01 AI 30039, N01AI30039] Funding Source: Medline

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Severe acute respiratory syndrome coronavirus (SCoV) 7a protein is one of the viral accessory proteins. In expressing cells, 7a protein exhibits a variety of biological activities, including induction of apoptosis, activation of the mitogen-activated protein kinase signaling pathway, inhibition of host protein translation, and suppression of cell growth progression. Analysis of SCoV particles that were purified by either sucrose gradient equilibrium centrifugation or a virus capture assay, in which intact SCoV particles were specifically immunoprecipitated by anti-S protein monoclonal antibody, demonstrated that 7a protein was associated with purified SCoV particles. Coexpression of 7a protein with SCoV S, M, N, and E proteins resulted in production of virus-like particles (VLPs) carrying 7a protein, while 7a protein was not released from cells expressing 7a protein alone. Although interaction between 7a protein and another SCoV accessory protein, 3a, has been reported, 3a protein was dispensable for assembly of 7a protein into VLPs. S protein was not required for the 7a protein incorporation into VLPs, and yet 7a protein interacted with S protein in coexpressing cells. These data established that, in addition to 3a protein, 7a protein was a SCoV accessory protein identified as a SCoV structural protein.

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