Substrate recognition and transport by multidrug resistance protein 1 (ABCC1)

被引:221
作者
Deeley, RG [1 ]
Cole, SPC [1 ]
机构
[1] Queens Univ, Inst Canc Res, Div Canc Biol & Genet, Kingston, ON K7L 3N6, Canada
关键词
multidrug resistance protein 1; leukotriene C-4; glutathione; atomic homology model; site-directed; mutagenesis; organic anion transport; ABC transporter; multidrug resistance;
D O I
10.1016/j.febslet.2005.12.036
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
Multidrug resistance protein (MRP) 1 belongs to the 'C' branch of the ABC transporter superfamily. MRP1 is a high-affinity transporter of the cysteinyl leukotriene C-4 and is responsible for the systemic release of this cytokine in response to an inflammatory stimulus. However, the substrate specificity of MRP1 is extremely broad and includes many organic anion conjugates of structurally unrelated endo- and xenobiotics. In addition, MRP1 transports unmodified hydrophobic compounds, such as natural product type chemotherapeutic agents and mutagens, such as aflatoxin B-1. Transport of several of these compounds has been shown to be dependent on the presence of reduced glutathione (GSH). More recently, GSH has also been shown to stimulate the transport of some conjugated compounds, including sulfates and glucuronides. Here, we summarize current knowledge of the substrate specificity and modes of transport of MRP1 and discuss how the protein may recognize its structurally diverse substrates. (c) 2005 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1103 / 1111
页数:9
相关论文
共 102 条
[1]   Membrane topology and glycosylation of the human multidrug resistance-associated protein [J].
Bakos, E ;
Hegedus, T ;
Hollo, Z ;
Welker, E ;
Tusnady, GE ;
Zaman, GJR ;
Flens, MJ ;
Varadi, A ;
Sarkadi, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (21) :12322-12326
[2]  
Bakos É, 2000, J CELL SCI, V113, P4451
[3]   Functional multidrug resistance protein (MRP1) lacking the N-terminal transmembrane domain [J].
Bakos, E ;
Evers, R ;
Szakács, G ;
Tusnády, GE ;
Welker, E ;
Szabó, K ;
de Haas, M ;
van Deemter, L ;
Borst, P ;
Váradi, A ;
Sarkadi, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (48) :32167-32175
[4]   Membrane transport proteins with complete replacement of transmembrane helices with polyalanine sequences remain functional [J].
Bao, XY ;
Chen, YY ;
Lee, SH ;
Lee, SC ;
Reuss, L ;
Altenberg, GA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (10) :8647-8650
[5]   Differential modulation of the human liver conjugate transporters MRP2 and MRP3 by bile acids and organic anions [J].
Bodó, A ;
Bakos, E ;
Szeri, F ;
Váradi, A ;
Sarkadi, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (26) :23529-23537
[6]   Molecular modeling correctly predicts the functional importance of Phe594 in transmembrane Helix 11 of the multidrug resistance protein, MRP1 (ABCC1) [J].
Campbell, JD ;
Koike, K ;
Moreau, C ;
Sansom, MSP ;
Deeley, RG ;
Cole, SPC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (01) :463-468
[7]   RETRACTED: Structure of MsbA from E-coli:: A homolog of the multidrug resistance ATP binding cassette (ABC) transporters (Retracted Article. See vol 314, pg 1875, 2006) [J].
Chang, G ;
Roth, CB .
SCIENCE, 2001, 293 (5536) :1793-1800
[8]   RETRACTED: Structure of MsbA from Vibrio cholera:: A multidrug resistance ABC transporter homolog in a closed conformation (Retracted Article. See vol 369, pg 596, 2007) [J].
Chang, G .
JOURNAL OF MOLECULAR BIOLOGY, 2003, 330 (02) :419-430
[9]   Reversal of drug resistance mediated by multidrug resistance protein (MRP) 1 by dual effects of agosterol A on MRP1 function [J].
Chen, ZS ;
Aoki, S ;
Komatsu, M ;
Ueda, K ;
Sumizawa, T ;
Furukawa, T ;
Okumura, H ;
Ren, XQ ;
Belinsky, MG ;
Lee, K ;
Kruh, GD ;
Kobayashi, M ;
Akiyama, S .
INTERNATIONAL JOURNAL OF CANCER, 2001, 93 (01) :107-113
[10]  
COLE SPC, 1994, CANCER RES, V54, P5902