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
相关论文
共 68 条
[1]  
AKIYAMA SI, 1988, MOL PHARMACOL, V33, P144
[2]   DISCRETE MUTATIONS INTRODUCED IN THE PREDICTED NUCLEOTIDE-BINDING SITES OF THE MDR1 GENE ABOLISH ITS ABILITY TO CONFER MULTIDRUG RESISTANCE [J].
AZZARIA, M ;
SCHURR, E ;
GROS, P .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (12) :5289-5297
[3]   EFFECTS OF INDOLE ALKALOIDS ON MULTIDRUG RESISTANCE AND LABELING OF P-GLYCOPROTEIN BY A PHOTOAFFINITY ANALOG OF VINBLASTINE [J].
BECK, WT ;
CIRTAIN, MC ;
GLOVER, CJ ;
FELSTED, RL ;
SAFA, AR .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 153 (03) :959-966
[4]  
BHAT UG, 1995, MOL PHARMACOL, V48, P682
[5]   INHIBITION OF ERYTHROCYTE GLUTATHIONE CONJUGATE TRANSPORT BY POLYETHOXYLATED SURFACTANTS [J].
BOARD, PG .
FEBS LETTERS, 1993, 315 (03) :298-300
[6]  
BOLLAG DM, 1995, CANCER RES, V55, P2325
[7]  
BORST P, 1995, ANNU REV MICROBIOL, V49, P427, DOI 10.1146/annurev.mi.49.100195.002235
[8]  
Buckingham LE, 1996, INT J CANCER, V65, P74
[9]   INTERNAL DUPLICATION AND HOMOLOGY WITH BACTERIAL TRANSPORT PROTEINS IN THE MDR1 (P-GLYCOPROTEIN) GENE FROM MULTIDRUG-RESISTANT HUMAN-CELLS [J].
CHEN, CJ ;
CHIN, JE ;
UEDA, K ;
CLARK, DP ;
PASTAN, I ;
GOTTESMAN, MM ;
RONINSON, IB .
CELL, 1986, 47 (03) :381-389
[10]  
CHIN KV, 1990, J BIOL CHEM, V265, P221