首页 | 本学科首页   官方微博 | 高级检索  
     


An in-depth analysis of the biological functional studies based on the NMR M2 channel structure of influenza A virus
Authors:Huang Ri-Bo  Du Qi-Shi  Wang Cheng-Hua  Chou Kuo-Chen
Affiliation:a Guangxi Academy of Sciences, 98 Daling Road, Nanning, Guangxi 530004, China
b College of Life Science and Technique, Guangxi University, 100 University Road, Nanning, Guangxi 530004, China
c College of Chemistry and Life Science, Tianjin Normal University, Tianjin, 300074, China
d Gordon Life Science Institute, San Diego, CA 92130, USA
Abstract:The long-sought three-dimensional structure of the M2 proton channel of influenza A virus was successfully determined recently by the high-resolution NMR [J.R. Schnell, J.J. Chou, Structure and mechanism of the M2 proton channel of influenza A virus, Nature 451 (2008) 591-595]. Such a milestone work has provided a solid structural basis for studying drug-resistance problems. However, the action mechanism revealed from the NMR structure is completely different from the traditional view and hence prone to be misinterpreted as “conflicting” with some previous biological functional studies. To clarify this kind of confusion, an in-depth analysis was performed for these functional studies, particularly for the mutations D44N, D44A and N44D on position 44, and the mutations on positions 27-38. The analyzed results have provided not only compelling evidences to further validate the NMR structure but also very useful clues for dealing with the drug-resistance problems and developing new effective drugs against H5N1 avian influenza virus, an impending threat to human beings.
Keywords:Membrane protein channel   Virus   Drug-resistance   Rimantadine   Molecular wedge   Allosteric inhibition mechanism   Long-range interaction
本文献已被 ScienceDirect PubMed 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号