Trincone Anna, Schwegmann-Weßels Christel
Institute for Virology, Department of Infectious Diseases, University of Veterinary Medicine Hannover, Bünteweg 17, 30559 Hannover, Germany.
Institute for Virology, Department of Infectious Diseases, University of Veterinary Medicine Hannover, Bünteweg 17, 30559 Hannover, Germany.
Virus Res. 2015 Apr 16;202:3-11. doi: 10.1016/j.virusres.2014.11.029. Epub 2014 Dec 4.
The spike protein S of transmissible gastroenteritis virus, an Alphacoronavirus, contains a tyrosine-based sorting signal that is responsible for ERGIC retention and may be important for a correct viral assembly process. To find out whether the S protein interacts with cellular proteins via this sorting signal, a pulldown assay with GST fusion proteins was performed. Filamin A has been identified as a putative interaction candidate. Immunofluorescence assays confirmed a co-localization between the TGEV S protein and filamin A. Further experiments have to be performed to prove a significant impact of filamin A on TGEV infection. Different approaches of several researchers for the identification of cellular interaction candidates relevant for coronavirus replication are summarized. These results may help in the future to identify the role of cellular proteins during coronavirus assembly at the ER-Golgi intermediate compartment.
可传播性胃肠炎病毒(一种甲型冠状病毒)的刺突蛋白S含有一个基于酪氨酸的分选信号,该信号负责内质网-高尔基体中间囊泡(ERGIC)滞留,并且可能对正确的病毒组装过程很重要。为了弄清楚S蛋白是否通过该分选信号与细胞蛋白相互作用,进行了用GST融合蛋白的下拉试验。细丝蛋白A已被确定为一个假定的相互作用候选物。免疫荧光试验证实了TGEV S蛋白与细丝蛋白A之间的共定位。必须进行进一步的实验来证明细丝蛋白A对TGEV感染的显著影响。总结了几位研究人员用于鉴定与冠状病毒复制相关的细胞相互作用候选物的不同方法。这些结果可能有助于未来确定细胞蛋白在冠状病毒于内质网-高尔基体中间囊泡组装过程中的作用。