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通过连续半胱氨酸诱变揭示的钠通道孔结构

Structure of the sodium channel pore revealed by serial cysteine mutagenesis.

作者信息

Pérez-García M T, Chiamvimonvat N, Marban E, Tomaselli G F

机构信息

Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

出版信息

Proc Natl Acad Sci U S A. 1996 Jan 9;93(1):300-4. doi: 10.1073/pnas.93.1.300.

Abstract

The pores of voltage-gated cation channels are formed by four intramembrane segments that impart selectivity and conductance. Remarkably little is known about the higher order structure of these critical pore-lining or P segments. Serial cysteine mutagenesis reveals a pattern of side-chain accessibility that contradicts currently favored structural models based on alpha-helices or beta-strands. Like the active sites of many enzymes of known structure, the sodium channel pore consists of irregular loop regions.

摘要

电压门控阳离子通道的孔道由四个膜内片段形成,这些片段赋予通道选择性和导电性。对于这些关键的孔道内衬或P片段的高级结构,人们所知甚少。连续半胱氨酸诱变揭示了一种侧链可及性模式,这与目前基于α螺旋或β链的主流结构模型相矛盾。与许多已知结构的酶的活性位点一样,钠通道孔道由不规则的环区组成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6384/40226/f8d949fba035/pnas01505-0312-a.jpg

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