Cornillez-Ty Cromwell T, Liao Lujian, Yates John R, Kuhn Peter, Buchmeier Michael J
Molecular and Integrative Neurosciences Department, The Scripps Research Institute, 10550 N. Torrey Pines Road, La Jolla, California 92037, USA.
J Virol. 2009 Oct;83(19):10314-8. doi: 10.1128/JVI.00842-09. Epub 2009 Jul 29.
The severe acute respiratory syndrome coronavirus (SARS-CoV) generates 16 nonstructural proteins (nsp's) through proteolytic cleavage of a large precursor protein. Although several nsp's exhibit catalytic activities that are important for viral replication and transcription, other nsp's have less clearly defined roles during an infection. In order to gain a better understanding of their functions, we attempted to identify host proteins that interact with nsp's during SARS-CoV infections. For nsp2, we identified an interaction with two host proteins, prohibitin 1 (PHB1) and PHB2. Our results suggest that nsp2 may be involved in the disruption of intracellular host signaling during SARS-CoV infections.
严重急性呼吸综合征冠状病毒(SARS-CoV)通过对一种大型前体蛋白进行蛋白水解切割产生16种非结构蛋白(nsp)。尽管几种nsp具有对病毒复制和转录很重要的催化活性,但其他nsp在感染过程中的作用尚不明确。为了更好地了解它们的功能,我们试图鉴定在SARS-CoV感染期间与nsp相互作用的宿主蛋白。对于nsp2,我们鉴定出它与两种宿主蛋白,即抑制素1(PHB1)和抑制素2(PHB2)相互作用。我们的结果表明,nsp2可能参与了SARS-CoV感染期间细胞内宿主信号传导的破坏。