Huang Ri-Bo, Du Qi-Shi, Wang Cheng-Hua, Chou Kuo-Chen
Guangxi Academy of Sciences, 98 Daling Road, Nanning, Guangxi 530004, China.
Biochem Biophys Res Commun. 2008 Dec 26;377(4):1243-7. doi: 10.1016/j.bbrc.2008.10.148. Epub 2008 Nov 6.
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.
甲型流感病毒M2质子通道长期以来一直寻求的三维结构最近通过高分辨率核磁共振成功确定[J.R.施内尔,J.J.周,甲型流感病毒M2质子通道的结构与机制,《自然》451(2008)591 - 595]。这样一项具有里程碑意义的工作为研究耐药性问题提供了坚实的结构基础。然而,从核磁共振结构揭示的作用机制与传统观点完全不同,因此容易被误解为与一些先前的生物学功能研究“相互矛盾”。为了澄清这种混淆,对这些功能研究进行了深入分析,特别是对第44位的D44N、D44A和N44D突变以及第27 - 38位的突变进行了分析。分析结果不仅为进一步验证核磁共振结构提供了令人信服的证据,也为应对耐药性问题以及开发针对H5N1禽流感病毒(对人类的一个迫在眉睫的威胁)的新型有效药物提供了非常有用的线索。