Structure of the multidrug resistance P-glycoprotein

被引:111
作者
Higgins, CF [1 ]
Callaghan, R
Linton, KJ
Rosenberg, MF
Ford, RC
机构
[1] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Clin Biochem, Oxford OX3 9DS, England
[2] Univ Oxford, John Radcliffe Hosp, Imperial Canc Res Fund Labs, Inst Mol Med, Oxford OX3 9DS, England
[3] Univ Manchester, Inst Sci & Technol, Dept Biochem & Appl Mol Biol, Manchester M60 1QD, Lancs, England
关键词
P-glycoprotein; protein structure; membrane protein; ABC transporters;
D O I
10.1006/scbi.1997.0067
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In order to elucidate the mechanism by which the multidrug resistance P-glycoprotein extrudes cytotoxic drugs from the cell, and particularly the number and nature of the drug binding site(s), knowledge of the structure of P-gp is essential. A considerable body of genetic and biochemical data has accrued which gives insights into P-gp structure and function. These data are critically reviewed, particularly in relation to the low resolution structure of P-gp which has recently been determined by electron microscopy. P-gp is one of the best characterised of the ABC transporters and these structure-function studies may have more general implications.
引用
收藏
页码:135 / 142
页数:8
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