《普通生理学杂志》前100年的载体、交换体和共转运体。

The Journal of General Physiology Pub Date : 2018-08-06 Epub Date: 2018-07-20 DOI:10.1085/jgp.201812078
Michael L Jennings
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引用次数: 6

摘要

转运蛋白、泵和通道是催化溶质跨膜运动的蛋白质。单溶质载体、偶联交换体和偶联共转运体统称为转运体,它们不同于导电离子通道、水通道和atp水解泵。研究转运体机制的主要概念框架是交替通路模型,该模型包括渗透屏障两侧的底物结合和释放事件以及涉及内向和外向构象状态之间构象变化的易位事件。1948年,《普通生理学杂志》开始发表关于红细胞葡萄糖转运体的研究,这是第一个被动力学表征的转运体,随后在20世纪60年代开始发表了关于速率、化学计量、不对称、电压依赖性和偶联交换体和共转运体调节的文章。在20世纪80年代cDNA克隆和测序出现之后,异种表达系统和定点诱变使得鉴定特定氨基酸残基的功能作用成为可能。在过去的二十年中,转运蛋白的结构使得在分子水平上提出转运蛋白功能的特定模型成为可能。在这里,我们回顾了JGP文章对我们目前对溶质转运机制的理解的贡献。无论主题是动力学、能量学、调控、诱变还是基于结构的建模,这些文章的一个共同特征是定量的、机械的方法,导致对转运蛋白功能的持久见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Carriers, exchangers, and cotransporters in the first 100 years of the <i>Journal of General Physiology</i>.

Carriers, exchangers, and cotransporters in the first 100 years of the <i>Journal of General Physiology</i>.

Carriers, exchangers, and cotransporters in the first 100 years of the <i>Journal of General Physiology</i>.

Carriers, exchangers, and cotransporters in the first 100 years of the Journal of General Physiology.
Transporters, pumps, and channels are proteins that catalyze the movement of solutes across membranes. The single-solute carriers, coupled exchangers, and coupled cotransporters that are collectively known as transporters are distinct from conductive ion channels, water channels, and ATP-hydrolyzing pumps. The main conceptual framework for studying transporter mechanisms is the alternating access model, which comprises substrate binding and release events on each side of the permeability barrier and translocation events involving conformational changes between inward-facing and outward-facing conformational states. In 1948, the Journal of General Physiology began to publish work that focused on the erythrocyte glucose transporter—the first transporter to be characterized kinetically—followed by articles on the rates, stoichiometries, asymmetries, voltage dependences, and regulation of coupled exchangers and cotransporters beginning in the 1960s. After the dawn of cDNA cloning and sequencing in the 1980s, heterologous expression systems and site-directed mutagenesis allowed identification of the functional roles of specific amino acid residues. In the past two decades, structures of transport proteins have made it possible to propose specific models for transporter function at the molecular level. Here, we review the contribution of JGP articles to our current understanding of solute transporter mechanisms. Whether the topic has been kinetics, energetics, regulation, mutagenesis, or structure-based modeling, a common feature of these articles has been a quantitative, mechanistic approach, leading to lasting insights into the functions of transporters.
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