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原核生物与真核生物钾离子通道之间的进化联系。

Evolutionary link between prokaryotic and eukaryotic K+ channels.

作者信息

Derst C, Karschin A

机构信息

Institute for Normal and Pathological Physiology, University of Marburg, Germany.

出版信息

J Exp Biol. 1998 Oct;201(Pt 20):2791-9.

PMID:9866872
Abstract

Considering the importance of K+ channels in controlling the crucial K+ gradient across the plasma membranes of all living cells, it comes as no surprise that, besides being present in every eukaryotic cell, these integral membrane proteins have recently also been identified in prokaryotes. Today, approximately a dozen successfully completed and many more ongoing sequencing projects permit a search for genes related to K+ channels in the genomes of both eubacteria and archaea. The coding regions of homologues show a remarkable variety in primary structure. They predict membrane proteins with one, two, three and six hydrophobic segments surrounding a putative K(+)-selective pore (H5) and the presence or absence of a cytosolic putative NAD(+)-binding domain (PNBD) that probably senses the reducing power of the cell. The analysis of kinships on the basis of phylogenetic algorithms identifies sequences closely related to eukaryotic voltage-dependent Kv channels, but also defines members of a primordial class of prokaryotic K+ channel (containing the 2TMS/PNBD motif). Considering the unique mechanisms that may account for the assembly of modern proteins from different ancestral genes, and with more primary sequence data soon to appear, a scheme for the evolutionary origin of K+ channels comes within reach.

摘要

鉴于钾离子通道对于控制所有活细胞跨质膜的关键钾离子梯度具有重要意义,这些整合膜蛋白除了存在于每个真核细胞中外,最近还在原核生物中被发现,这也就不足为奇了。如今,大约有十几个已成功完成以及更多正在进行的测序项目,使得人们能够在真细菌和古细菌的基因组中寻找与钾离子通道相关的基因。同源物的编码区在一级结构上表现出显著的多样性。它们预测的膜蛋白具有一个、两个、三个和六个围绕假定的钾离子选择性孔(H5)的疏水片段,以及一个胞质假定的NAD⁺结合结构域(PNBD)的存在与否,该结构域可能感知细胞的还原能力。基于系统发育算法的亲缘关系分析确定了与真核电压依赖性Kv通道密切相关的序列,但也定义了原核钾离子通道原始类别的成员(包含2TMS/PNBD基序)。考虑到可能解释由不同祖先基因组装现代蛋白质的独特机制,并且随着更多一级序列数据即将出现,钾离子通道的进化起源方案已触手可及。

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