Aquaporins - Expression, purification and characterization

被引:17
作者
Bill, Roslyn M. [1 ]
Hedfalk, Kristina [2 ]
机构
[1] Aston Univ, Coll Hlth & Life Sci, Birmingham B4 7ET, W Midlands, England
[2] Gothenburg Univ, Dept Chem & Mol Biol, Box 462, S-40530 Gothenburg, Sweden
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2021年 / 1863卷 / 09期
基金
瑞典研究理事会; 英国生物技术与生命科学研究理事会;
关键词
Aquaporin; Water channel; Recombinant production; Proteoliposomes; X-RAY-STRUCTURE; PRELIMINARY CRYSTALLOGRAPHIC ANALYSIS; EUKARYOTIC MEMBRANE-PROTEINS; WATER-CHANNEL; STRUCTURAL BASIS; CRYSTAL-STRUCTURE; SELECTIVITY; CRYSTALLIZATION; RECONSTITUTION; RESOLUTION;
D O I
10.1016/j.bbamem.2021.183650
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aquaporin water channels facilitate the bi-directional flow of water and small, neutral solutes down an osmotic gradient in all kingdoms of life. Over the last two decades, the availability of high-quality protein has underpinned progress in the structural and functional characterization of these water channels. In particular, recombinant protein technology has guaranteed the supply of aquaporin samples that were of sufficient quality and quantity for further study. Here we review the features of successful expression, purification and characterization strategies that have underpinned these successes and that will drive further breakthroughs in the field. Overall, Escherichia coli is a suitable host for prokaryotic isoforms, while Pichia pastoris is the most commonly-used recombinant host for eukaryotic variants. Generally, a two-step purification procedure is suitable after solubilization in glucopyranosides and most structures are determined by X-ray following crystallization.
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页数:10
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