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离子稳态、通道与转运体:细胞机制的最新进展

Ion homeostasis, channels, and transporters: an update on cellular mechanisms.

作者信息

Dubyak George R

机构信息

Department of Physiology and Biophysics, School of Medicine, Case Western Reserve University, 2119 Abington Road, Cleveland, OH 44106-4970, USA.

出版信息

Adv Physiol Educ. 2004 Dec;28(1-4):143-54. doi: 10.1152/advan.00046.2004.

Abstract

The steady-state maintenance of highly asymmetric concentrations of the major inorganic cations and anions is a major function of both plasma membranes and the membranes of intracellular organelles. Homeostatic regulation of these ionic gradients is critical for most functions. Due to their charge, the movements of ions across biological membranes necessarily involves facilitation by intrinsic membrane transport proteins. The functional characterization and categorization of membrane transport proteins was a major focus of cell physiological research from the 1950s through the 1980s. On the basis of these functional analyses, ion transport proteins were broadly divided into two classes: channels and carrier-type transporters (which include exchangers, cotransporters, and ATP-driven ion pumps). Beginning in the mid-1980s, these functional analyses of ion transport and homeostasis were complemented by the cloning of genes encoding many ion channels and transporter proteins. Comparison of the predicted primary amino acid sequences and structures of functionally similar ion transport proteins facilitated their grouping within families and superfamilies of structurally related membrane proteins. Postgenomics research in ion transport biology increasingly involves two powerful approaches. One involves elucidation of the molecular structures, at the atomic level in some cases, of model ion transport proteins. The second uses the tools of cell biology to explore the cell-specific function or subcellular localization of ion transport proteins. This review will describe how these approaches have provided new, and sometimes surprising, insights regarding four major questions in current ion transporter research. 1) What are the fundamental differences between ion channels and ion transporters? 2) How does the interaction of an ion transport protein with so-called adapter proteins affect its subcellular localization or regulation by various intracellular signal transduction pathways? 3) How does the specific lipid composition of the local membrane microenvironment modulate the function of an ion transport protein? 4) How can the basic functional properties of a ubiquitously expressed ion transport protein vary depending on the cell type in which it is expressed?

摘要

维持主要无机阳离子和阴离子高度不对称的浓度稳态是质膜和细胞内细胞器膜的一项主要功能。这些离子梯度的稳态调节对大多数功能至关重要。由于离子带电,其跨生物膜的移动必然需要内在膜转运蛋白的协助。从20世纪50年代到80年代,膜转运蛋白的功能特性和分类一直是细胞生理学研究的主要焦点。基于这些功能分析,离子转运蛋白大致分为两类:通道和载体型转运蛋白(包括交换体、协同转运体和ATP驱动的离子泵)。从20世纪80年代中期开始,对离子转运和稳态的这些功能分析通过克隆许多离子通道和转运蛋白的编码基因得到了补充。对功能相似的离子转运蛋白预测的一级氨基酸序列和结构进行比较,有助于将它们归类到结构相关膜蛋白的家族和超家族中。离子转运生物学的后基因组学研究越来越多地涉及两种强大的方法。一种方法涉及在某些情况下在原子水平阐明模型离子转运蛋白的分子结构。第二种方法使用细胞生物学工具来探索离子转运蛋白的细胞特异性功能或亚细胞定位。本综述将描述这些方法如何为当前离子转运蛋白研究中的四个主要问题提供了新的、有时令人惊讶的见解。1)离子通道和离子转运蛋白之间的根本区别是什么?2)离子转运蛋白与所谓的衔接蛋白的相互作用如何影响其亚细胞定位或通过各种细胞内信号转导途径进行调节?3)局部膜微环境的特定脂质组成如何调节离子转运蛋白的功能?4)普遍表达的离子转运蛋白的基本功能特性如何根据其表达的细胞类型而变化?

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