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Multidrug resistance protein 1 is not associated to detergent-resistant membranes
Authors:Cerf Emilie  Gasper Régis  Belani Jitendra D  Rychnovsky Scott  Chang Xiu-Bao  Buyse Frédéric  Ruysschaert Jean-Marie
Institution:Structure et Fonction des Membranes Biologiques, Centre de Biologie Structurale et de Bioinformatique, Université Libre de Bruxelles, Boulevard du Triomphe, B-1050 Brussels, Belgium.
Abstract:Multidrug resistance protein 1 (MRP1) is a member of the ATP-binding cassette superfamily. Using the energy provided by ATP hydrolysis, it transports a broad spectrum of substrates across the plasma membrane, including hormones, leukotriene C(4), bile salts, and anti-cancer drugs. Recent works have suggested that P-glycoprotein is associated to cholesterol and sphingolipid-rich membrane microdomains and that cholesterol upregulates its ATPase and drug transport activities. Confocal microscopy experiments and Triton X-100 extraction of detergent-resistant membranes provide evidence that MRP1 is not located in raft-like structures and that its activity is downregulated by cholesterol. The data are discussed in terms of cholesterol-protein interaction and topology.
Keywords:ABC  ATP-binding cassette  AMP  adenosine monophosphate  ATP  adenosine triphosphate  CFTR  cystic fibrosis transmembrane conductance regulator  CRAC  cholesterol recognition/interaction amino acid consensus  DRM  detergent-resistant membrane  HEK  human embryonic kidney  LTC4  leukotriene C4  MβCD  methyl-β-cyclodextrin  MDR  multidrug resistance  MRP  Multidrug resistance protein  NBD  nucleotide-binding domain  Pgp  P-glycoprotein  SSD  sterol sensing domain  TMD  transmembrane domain
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