Yuan Xiaoling, Li Jianyong, Shan Yajun, Yang Zhen, Zhao Zhenhu, Chen Bo, Yao Zhenyu, Dong Bo, Wang Shengqi, Chen Jiapei, Cong Yuwen
Department of Pathophysiology, Beijing Institute of Radiation Medicine, No. 27 Taiping Road, Beijing, 100850, China.
Virus Res. 2005 May;109(2):191-202. doi: 10.1016/j.virusres.2005.01.001.
SARS-CoV 3a protein was a unique protein of SARS coronavirus (SARS-CoV), which was identified in SARS-CoV infected cells and SARS patients' specimen. Recent studies revealed that 3a could interact specifically with many SARS-CoV structural proteins, such as M, E and S protein. Expressed 3a protein was reported to localize to Golgi complex in SARS-CoV infected cells. In this study, it was shown that 3a protein was mainly located in Golgi apparatus with different tags at N- or C-terminus. The localization pattern was similar in different transfected cells. With the assay of truncated 3a protein, it was shown that 3a might contain three transmembrane regions, and the second or third region was properly responsible for Golgi localization. By ultra-centrifugation experiment with different extraction buffers, it was confirmed that 3a was an integral membrane protein and embedded in the phospholipid bilayer. Immunofluorescence assay indicated that 3a was co-localized with M protein in Golgi complex in co-transfected cells. These results provide a new insight for further study of the 3a protein on the pathogenesis of SARS-CoV.
严重急性呼吸综合征冠状病毒(SARS-CoV)的3a蛋白是SARS冠状病毒(SARS-CoV)的一种独特蛋白,在SARS-CoV感染的细胞和SARS患者的标本中被鉴定出来。最近的研究表明,3a蛋白可以与许多SARS-CoV结构蛋白特异性相互作用,如M、E和S蛋白。据报道,在SARS-CoV感染的细胞中,表达的3a蛋白定位于高尔基体复合物。在本研究中,结果表明,在N端或C端带有不同标签的3a蛋白主要位于高尔基体。在不同的转染细胞中,定位模式相似。通过对截短的3a蛋白的检测,结果表明3a蛋白可能含有三个跨膜区域,第二个或第三个区域对高尔基体定位起主要作用。通过使用不同提取缓冲液的超速离心实验,证实3a是一种整合膜蛋白,嵌入磷脂双分子层中。免疫荧光检测表明,在共转染细胞中,3a蛋白与M蛋白在高尔基体复合物中共定位。这些结果为进一步研究3a蛋白在SARS-CoV发病机制中的作用提供了新的见解。