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

Journal

FEBS LETTERS
Volume 580, Issue 4, Pages 1103-1111

Publisher

WILEY
DOI: 10.1016/j.febslet.2005.12.036

Keywords

multidrug resistance protein 1; leukotriene C-4; glutathione; atomic homology model; site-directed; mutagenesis; organic anion transport; ABC transporter; multidrug resistance

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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.

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