Huang Cheng, Narayanan Krishna, Ito Naoto, Peters C J, Makino Shinji
Department of Microbiology and Immunology, The University of Texas Medical Branch at Galveston, Galveston, TX 77555-1019, USA.
J Virol. 2006 Jan;80(1):210-7. doi: 10.1128/JVI.80.1.210-217.2006.
Severe acute respiratory syndrome coronavirus (SCoV) accessory protein 3a is a virus structural protein. We demonstrate here that 3a protein was released efficiently in membranous structures from various cell lines expressing 3a protein. A subpopulation of the released 3a protein is associated with detergent-resistant membranes. The presence of the YxxPhi and diacidic motifs, located within the cytoplasmic tail of the 3a protein, was not required for its efficient release. Analysis of supernatant from SCoV-infected cells with sucrose gradient sedimentation and virus capture assay indicated that the 3a protein was released from infected cells in two distinct populations, as a component of SCoV particles, and in membrane structures with a lower buoyant density. These data provide new insights into the biological properties of SCoV 3a protein.
严重急性呼吸综合征冠状病毒(SCoV)辅助蛋白3a是一种病毒结构蛋白。我们在此证明,3a蛋白在表达3a蛋白的各种细胞系的膜结构中有效释放。释放的3a蛋白的一个亚群与抗去污剂膜相关。3a蛋白胞质尾内的YxxPhi和双酸性基序的存在并非其有效释放所必需。用蔗糖梯度沉降和病毒捕获试验分析SCoV感染细胞的上清液表明,3a蛋白以两种不同的群体从感染细胞中释放出来,作为SCoV颗粒的一个组成部分,并存在于浮力密度较低的膜结构中。这些数据为SCoV 3a蛋白的生物学特性提供了新的见解。