Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1935885 | Biochemical and Biophysical Research Communications | 2008 | 5 Pages |
Abstract
Severe acute respiratory syndrome-associated coronavirus (SARS-CoV) is responsible for SARS infection. Nucleocapsid (N) protein of SARS-CoV encapsidates the viral RNA and plays an important role in virus particle assembly and release. In this study, the N protein of SARS-CoV was found to associate with B23, a phosphoprotein in nucleolus, in vitro and in vivo. Mapping studies localized the critical N sequences for this interaction to amino acid residues 175–210, which included a serine/arginine (SR)-rich domain. In vitro phosphorylation assay showed that the N protein inhibited the B23 phosphorylation at Thr199.
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Authors
Yingchun Zeng, Linbai Ye, Shengli Zhu, Hong Zheng, Peng Zhao, Weijia Cai, Liya Su, Yinglong She, Zhenghui Wu,