How does P-glycoprotein recognize its substrates?

被引:105
作者
Ueda, K [1 ]
Taguchi, Y [1 ]
Morishima, M [1 ]
机构
[1] Kyoto Univ, Grad Sch Agr, Div Appl Life Sci, Biochem Lab, Kyoto 60601, Japan
关键词
flippase; multidrug resistance; P-glycoprotein; substrate specificity; transporter;
D O I
10.1006/scbi.1997.0066
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We review how P-glycoprotein recognizes a wide variety of compounds and how it carries its substrates across membranes. Amino acid substitutions that affect the substrate specificity of P-glycoprotein have been found scattered throughout the molecule. In particular, some amino acid residues in the putative transmembrane domain (TM)1 together with TM5-6 and TM11-12 may help to govern substrate specificity. The features that substrates for P-glycoprotein share are also discussed. The amphipathy of a substrate may decide whether the substrate can be intercalated into the lipid bilayer of the membrane. In addition, only certain molecular volumes and tertiary structures may mab it possible for the substrate to fit into the substrate-binding site(s) of P-glycoprotein.
引用
收藏
页码:151 / 159
页数:9
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