Transport of haloacids across biological membranes

被引:6
|
作者
Su, Xianbin [1 ]
Li, Ruihong [2 ]
Kong, Ka-Fai [3 ]
Tsang, Jimmy S. H. [3 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Ctr Syst Biomed, Key Lab Syst Biomed, Minist Educ, Shanghai 200240, Peoples R China
[2] Shanghai Qual Safety Ctr Agr Prod, Shanghai 200335, Peoples R China
[3] Univ Hong Kong, Sch Biol Sci, Mol Microbiol Lab, Pokfulam Rd, Hong Kong, Hong Kong, Peoples R China
来源
关键词
Haloacids transporter; Carboxylate transporter; MCTI; SLC5A8; Deh4p; Dehp2; MITOCHONDRIAL PYRUVATE CARRIER; PSEUDOMONAS-PUTIDA PP3; INTRACELLULAR PH INDICATOR; CONTROLLED CLINICAL-TRIAL; AMINO-ACID-TRANSPORT; FLUORO-BETA-ALANINE; PERFUSED RAT-LIVER; ESCHERICHIA-COLI; ANTITUMOR-ACTIVITY; DEHALOGENASE GENE;
D O I
10.1016/j.bbamem.2016.09.017
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
Haloacids are considered to be environmental pollutants, but some of them have also been tested in clinical research. The way that haloacids are transported across biological membranes is important for both biodegradation and drug delivery purposes. In this review, we will first summarize putative haloacids transporters and the information about haloacids transport when studying carboxylates transporters. We will then introduce MCT1 and SLC5A8, which are respective transporter for antitumor agent 3-bromopyruvic acid and dichloroacetic acid, and monochloroacetic acid transporters Deh4p and Dehp2 from a haloacids-degrading bacterium. Phylogenetic analysis of these haloacids transporters and other monocarboxylate transporters reveals their evolutionary relationships. Haloacids transporters are not studied to the extent that they deserve compared with their great application potentials, thus future inter-discipline research are desired to better characterize their transport mechanisms for potential applications in both environmental and clinical fields. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:3061 / 3070
页数:10
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