Transmembrane remote conformational suppression of the Gly-332 mutation of the Tn10-encoded metal-tetracycline/H+ antiporter

被引:9
作者
Kawabe, T
Yamaguchi, A
机构
[1] Osaka Univ, Inst Sci & Ind Res, Dept Cell Membrane Biol, Ibaraki, Osaka 567, Japan
[2] Osaka Univ, Fac Pharmaceut Sci, Suita, Osaka 567, Japan
来源
FEBS LETTERS | 1999年 / 457卷 / 01期
关键词
tetracycline; drug resistance; drug export; site-directed mutagenesis;
D O I
10.1016/S0014-5793(99)01032-7
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
Gly-332 is a conformationally important residue of the Tn10-encoded metal-tetracycline/H+ antiporter (TetA(B)), which was found by random mutagenesis and confirmed by site-directed mutagenesis, A bulky side chain at position 332 is deleterious to the transport function. A spontaneous second-site suppressor revertant was isolated from G332S mutant and identified as the Ala-354 --> Asp mutant, Gly-332 and Ala-354 are located on opposite ends of transmembrane segment XI, As judged from [C-14]NEM binding to Cys mutants, the residue at position 354, which is originally exposed to water, was buried in the membrane by a G332S mutation through a remote conformational change of transmembrane segment XI, This effect is the same as that of a G62L mutation at position 30 through transmembrane segment II [Kimura, T,, Sawai, T, and Yamaguchi, A. (1997) Biochemistry 36, 6941-6946], Interestingly, the G332S mutation mas also suppressed by the L30S mutation, and the G62L mutation was moderately suppressed by the A354D mutation. These results indicate the presence of a close conformational relationship between the flanking regions of the transmembrane segments II and XI. (C) 1999 Federation of European Biochemical Societies.
引用
收藏
页码:169 / 173
页数:5
相关论文
共 31 条