Recent progress in understanding the mechanism of P-glycoprotein-mediated drug efflux

被引:179
作者
Loo, TW
Clarke, DM [1 ]
机构
[1] Univ Toronto, Dept Med, Toronto, ON, Canada
[2] Univ Toronto, Dept Biochem, Toronto, ON, Canada
关键词
P-glycoprotein; ABC transporter; substrate binding pocket; ATPase activity; thiol cross-linking; induced-fit mechanism;
D O I
10.1007/s00232-005-0792-1
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
P-glycoprotein (P-gp) is an ATP-dependent drug pump that can transport a broad range of hydrophobic compounds out of the cell. The protein is clinically important because of its contribution to the phenomenon of multidrug resistance during AIDS/HIV and cancer chemotherapy. P-gp is a member of the ATP-binding cassette (ABC) family of proteins. It is a single polypeptide that contains two repeats joined by a linker region. Each repeat has a transmembrane domain consisting of six transmembrane segments followed by a hydrophilic domain containing the nucleotide-binding domain. In this mini-review, we discuss recent progress in determining the structure and mechanism of human P-glycoprotein.
引用
收藏
页码:173 / 185
页数:13
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