Liu Ying, Yang Jichun, Chen Li-Ming
Key Laboratory of Molecular Biophysics of Ministry of Education, Department of Biophysics and Molecular Physiology, School of Life Science and Technology, Huazhong University of Science and TechnologyWuhan, China.
Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University Health Science CenterBeijing, China.
Front Physiol. 2015 Dec 1;6:355. doi: 10.3389/fphys.2015.00355. eCollection 2015.
The solute carrier SLC4 family consists of 10 members, nine of which are [Formula: see text] transporters, including three Na(+)-independent Cl(-)/[Formula: see text] exchangers AE1, AE2, and AE3, five Na(+)-coupled [Formula: see text] transporters NBCe1, NBCe2, NBCn1, NBCn2, and NDCBE, as well as "AE4" whose Na(+)-dependence remains controversial. The SLC4 [Formula: see text] transporters play critical roles in pH regulation and transepithelial movement of electrolytes with a broad range of demonstrated physiological relevances. Dysfunctions of these transporters are associated with a series of human diseases. During the past decades, tremendous amount of effort has been undertaken to investigate the topological organization of the SLC4 transporters in the plasma membrane. Based upon the proposed topology models, mutational and functional studies have identified important structural elements likely involved in the ion translocation by the SLC4 transporters. In the present article, we review the advances during the past decades in understanding the structure and function of the SLC4 transporters.
溶质载体SLC4家族由10个成员组成,其中9个是[公式:见正文]转运蛋白,包括3种不依赖Na⁺的Cl⁻/[公式:见正文]交换体AE1、AE2和AE3,5种与Na⁺偶联的[公式:见正文]转运蛋白NBCe1、NBCe2、NBCn1、NBCn2和NDCBE,以及其对Na⁺的依赖性仍存在争议的“AE4”。SLC4[公式:见正文]转运蛋白在pH调节和电解质的跨上皮转运中发挥关键作用,具有广泛的已证实的生理相关性。这些转运蛋白的功能障碍与一系列人类疾病相关。在过去几十年中,人们付出了巨大努力来研究SLC4转运蛋白在质膜中的拓扑结构。基于提出的拓扑模型,突变和功能研究已经确定了可能参与SLC4转运蛋白离子转运的重要结构元件。在本文中,我们综述了过去几十年在理解SLC4转运蛋白的结构和功能方面取得的进展。