Bakos Eva, Homolya László
Institute of Enzymology, Hungarian Academy of Sciences, Budapest, Hungary.
Pflugers Arch. 2007 Feb;453(5):621-41. doi: 10.1007/s00424-006-0160-8. Epub 2006 Dec 23.
MRP1 (ABCC1) is a peculiar member of the ABC transporter superfamily for several aspects. This protein has an unusually broad substrate specificity and is capable of transporting not only a wide variety of neutral hydrophobic compounds, like the MDR1/P-glycoprotein, but also facilitating the extrusion of numerous glutathione, glucuronate, and sulfate conjugates. The transport mechanism of MRP1 is also complex; a composite substrate-binding site permits both cooperativity and competition between various substrates. This versatility and the ubiquitous tissue distribution make this transporter suitable for contributing to various physiological functions, including defense against xenobiotics and endogenous toxic metabolites, leukotriene-mediated inflammatory responses, as well as protection from the toxic effect of oxidative stress. In this paper, we give an overview of the considerable amount of knowledge which has accumulated since the discovery of MRP1 in 1992. We place special emphasis on the structural features essential for function, our recent understanding of the transport mechanism, and the numerous assignments of this transporter.
多药耐药相关蛋白1(ABCC1)在多个方面都是ABC转运蛋白超家族中的一个特殊成员。该蛋白具有异常广泛的底物特异性,不仅能够转运多种中性疏水化合物,如多药耐药蛋白1/ P-糖蛋白,还能促进大量谷胱甘肽、葡萄糖醛酸和硫酸盐结合物的外排。多药耐药相关蛋白1的转运机制也很复杂;一个复合底物结合位点允许各种底物之间存在协同作用和竞争。这种多功能性以及在组织中的广泛分布使得该转运蛋白适合参与多种生理功能,包括对外源生物和内源性有毒代谢物的防御、白三烯介导的炎症反应,以及免受氧化应激的毒性作用。在本文中,我们概述了自1992年发现多药耐药相关蛋白1以来积累的大量知识。我们特别强调了对其功能至关重要的结构特征、我们对转运机制的最新理解,以及该转运蛋白的众多功能。