A general pattern for substrate recognition by P-glycoprotein

被引:457
|
作者
Seelig, A [1 ]
机构
[1] Univ Basel, Bioctr, Dept Biophys Chem, CH-4056 Basel, Switzerland
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1998年 / 251卷 / 1-2期
关键词
P-glycoprotein; substrate recognition; recognition pattern; hydrogen bonding; multidrug resistance;
D O I
10.1046/j.1432-1327.1998.2510252.x
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 actively transports a wide variety of chemically diverse compounds out of the cell. Based on a comparison of a hundred compounds previously tested as P-glycoprotein substrates, we suggest that a set of well-defined structural elements is required for an interaction with P-glycoprotein. The recognition elements are formed by two (type I unit) or three electron donor groups (type II unit) with a fixed spatial separation. Type I units consist of two electron donor groups with a spatial separation of 2.5+/-0.3 Angstrom. Type II units contain either two electron donor groups with a spatial separation of 4.6+/-0.6 Angstrom or three electron donor groups with a spatial separation of the outer two groups of 4.6+/-0.6 Angstrom. All molecules that contain at least one type I or one type II unit are predicted to be P-glycoprotein substrates. The binding to P-glycoprotein increases with the strength and the number of electron donor or hydrogen bonding acceptor groups forming the type I and type II units. Correspondingly, a high percentage of amino acids with hydrogen bonding donor side chains is found in the transmembrane sequences of P-glycoprotein relevant for substrate interaction. Molecules that minimally contain one type II unit are predicted to be inducers of P-glycoprotein over-expression.
引用
收藏
页码:252 / 261
页数:10
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