Mechanisms of drug/H+ antiport: complete cysteine-scanning mutagenesis and the protein engineering approach.

Abstract:

:The notorious difficulty of elucidating structures of membrane transporters by crystallography has long prevented our understanding of active transport mechanism coupled with ion/proton transport. The determination of the first crystal structure of the drug/H+ antiporter AcrB was a breakthrough for structure-based understanding of drug/H+ antiport. However, although AcrB is a major multidrug exporter in Gram-negative organisms, the majority of bacterial drug exporters are major facilitator superfamily (MFS) drug transporters. As no crystal structures have been solved for MFS transporters, the alternative protein-engineering methods are still very useful for estimating structures and functions of drug/H+ antiporters. This review describes this alternative approach for investigating the structure and function of tetracycline/H+ antiporters.

journal_name

Curr Opin Chem Biol

authors

Tamura N,Konishi S,Yamaguchi A

doi

10.1016/j.cbpa.2003.08.014

subject

Has Abstract

pub_date

2003-10-01 00:00:00

pages

570-9

issue

5

eissn

1367-5931

issn

1879-0402

pii

S1367593103001170

journal_volume

7

pub_type

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