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本文引用的文献

1
Transmembrane communication: general principles and lessons from the structure and function of the M2 proton channel, K⁺ channels, and integrin receptors.跨膜通讯:从 M2 质子通道、钾离子通道和整合素受体的结构与功能中得到的一般原理和启示。
Annu Rev Biochem. 2011;80:211-37. doi: 10.1146/annurev-biochem-091008-152423.
2
Multiple Proton Confinement in the M2 Channel from the Influenza A Virus.甲型流感病毒M2通道中的多质子限制
J Phys Chem C Nanomater Interfaces. 2010 Oct 21;114(48):20856-20863. doi: 10.1021/jp107431g.
3
Insight into the mechanism of the influenza A proton channel from a structure in a lipid bilayer.从脂质双层中的结构深入了解甲型流感质子通道的机制。
Science. 2010 Oct 22;330(6003):509-12. doi: 10.1126/science.1191750.
4
Mechanisms of proton conduction and gating in influenza M2 proton channels from solid-state NMR.固态 NMR 研究流感 M2 质子通道的质子传导和门控机制。
Science. 2010 Oct 22;330(6003):505-8. doi: 10.1126/science.1191714.
5
Ion binding to KcsA: implications in ion selectivity and channel gating.离子与 KcsA 的结合:对离子选择性和通道门控的影响。
Biochemistry. 2010 Nov 9;49(44):9480-7. doi: 10.1021/bi101235v.
6
Conformational plasticity of the influenza A M2 transmembrane helix in lipid bilayers under varying pH, drug binding, and membrane thickness.甲型流感病毒M2跨膜螺旋在不同pH值、药物结合及膜厚度条件下脂质双层中的构象可塑性
Biochim Biophys Acta. 2011 Jan;1808(1):415-23. doi: 10.1016/j.bbamem.2010.09.014. Epub 2010 Sep 29.
7
Influenza virus M2 protein mediates ESCRT-independent membrane scission.流感病毒 M2 蛋白介导了不依赖于 ESCRT 的膜分裂。
Cell. 2010 Sep 17;142(6):902-13. doi: 10.1016/j.cell.2010.08.029.
8
Solution NMR structure of the V27A drug resistant mutant of influenza A M2 channel.甲型流感 M2 通道 V27A 耐药突变体的溶液 NMR 结构。
Biochem Biophys Res Commun. 2010 Oct 8;401(1):58-63. doi: 10.1016/j.bbrc.2010.09.008. Epub 2010 Sep 15.
9
Influence of solubilizing environments on membrane protein structures.增溶环境对膜蛋白结构的影响。
Trends Biochem Sci. 2011 Feb;36(2):117-25. doi: 10.1016/j.tibs.2010.07.005. Epub 2010 Aug 18.
10
Proton and cation transport activity of the M2 proton channel from influenza A virus.甲型流感病毒 M2 质子通道的质子和阳离子转运活性。
Proc Natl Acad Sci U S A. 2010 Aug 31;107(35):15409-14. doi: 10.1073/pnas.1009997107. Epub 2010 Aug 16.

甲型流感病毒 M2 质子通道的功能和抑制的结构与动力学机制。

Structural and dynamic mechanisms for the function and inhibition of the M2 proton channel from influenza A virus.

机构信息

Department of chemistry, University of Pennsylvania, 231 south, 34th st, Philadelphia, PA 19104, USA.

出版信息

Curr Opin Struct Biol. 2011 Feb;21(1):68-80. doi: 10.1016/j.sbi.2010.12.002. Epub 2011 Jan 17.

DOI:10.1016/j.sbi.2010.12.002
PMID:21247754
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3039100/
Abstract

The M2 proton channel from influenza A virus, a prototype for a class of viral ion channels known as viroporins, conducts protons along a chain of water molecules and ionizable sidechains, including His37. Recent studies highlight a delicate interplay between protein folding, proton binding, and proton conduction through the channel. Drugs inhibit proton conduction by binding to an aqueous cavity adjacent to M2's proton-selective filter, thereby blocking access of proton to the filter, and altering the energetic landscape of the channel and the energetics of proton-binding to His37.

摘要

甲型流感病毒的 M2 质子通道是一类被称为病毒离子通道的病毒通道的原型,它沿着一系列水分子和可离子化侧链(包括 His37)传导质子。最近的研究强调了蛋白质折叠、质子结合以及质子通过通道传导之间的微妙相互作用。药物通过与 M2 的质子选择性过滤器相邻的水腔结合来抑制质子传导,从而阻止质子进入过滤器,并改变通道的能量景观以及质子与 His37 结合的能量。