Rowse Michael, Qiu Shihong, Tsao Jun, Yamauchi Yohei, Wang Guoxin, Luo Ming
Department of Microbiology, University of Alabama at Birmingham , 1025 18th Street South, Birmingham, Alabama 35294, United States.
Institute of Biochemistry, ETH Zurich , HPM E8.2, Otto-Stern-Weg 3, 8093 Zurich, Switzerland.
ACS Infect Dis. 2016 Jan 8;2(1):47-53. doi: 10.1021/acsinfecdis.5b00109. Epub 2015 Oct 22.
During cell entry of an enveloped virus, the viral membrane must be fused with the cellular membrane. The virus envelope has a unique structure consisting of viral proteins and a virus-specific lipid composition, whereas the host membrane has its own structure with host membrane proteins. Compound 136 was previously found to bind in close proximity to the viral envelope and inhibit influenza virus entry. We showed here that the 136-treated influenza virus still caused hemolysis. When liposomes were used as the target membrane for 136-treated viruses, aberrant fusion occurred; few liposomes fused per virion, and glycoproteins were not distributed evenly across fusion complexes. Additionally, large fusion aggregates did not form, and in some instances, neck-like structures were found. Based on previous results and hemolysis, fusion inhibition by 136 occurs post-scission but prior to lipid mixing.
在包膜病毒进入细胞的过程中,病毒膜必须与细胞膜融合。病毒包膜具有独特的结构,由病毒蛋白和病毒特异性脂质组成,而宿主膜则有其自身带有宿主膜蛋白的结构。先前发现化合物136在病毒包膜附近结合并抑制流感病毒进入。我们在此表明,经136处理的流感病毒仍会引起溶血。当脂质体用作经136处理的病毒的靶膜时,会发生异常融合;每个病毒粒子融合的脂质体很少,并且糖蛋白在融合复合物中分布不均匀。此外,没有形成大的融合聚集体,并且在某些情况下,发现了颈部样结构。根据先前的结果和溶血情况,136对融合的抑制作用发生在切割后但脂质混合之前。