Webb Tom R, Clark Adrian J L
Centre for Endocrinology, John Vane Science Centre, Charterhouse Square, London EC1M6BQ, United Kingdom.
Mol Endocrinol. 2010 Mar;24(3):475-84. doi: 10.1210/me.2009-0283. Epub 2009 Oct 23.
The melanocortin 2 receptor (MC2R) accessory protein, MRAP, is one of a growing number of G protein-coupled receptor accessory proteins that have been identified in recent years that add control and complexity to G protein-coupled receptor functional expression and signal transduction. MRAP interacts directly with MC2R and is essential for its trafficking from the endoplasmic reticulum to the cell surface, where it acts as the receptor for the pituitary hormone ACTH. In addition, MRAP2, a newly described homolog of MRAP, is also able to support the cell surface expression of MC2R. Although it is clear that MRAP is required for MC2R function, the mechanism of MRAP action is only beginning to be understood. Recent work has started to reveal some of these mechanisms and the MRAP domains involved in MC2R functional expression, and new data have shown a potential role for both MRAP and MRAP2 in the regulation of the other melanocortin receptors.
黑皮质素2受体(MC2R)辅助蛋白MRAP是近年来发现的越来越多的G蛋白偶联受体辅助蛋白之一,这些蛋白为G蛋白偶联受体的功能表达和信号转导增加了调控和复杂性。MRAP直接与MC2R相互作用,对于其从内质网运输到细胞表面至关重要,在细胞表面它作为垂体激素促肾上腺皮质激素(ACTH)的受体发挥作用。此外,MRAP2是新发现的MRAP同源物,也能够支持MC2R在细胞表面的表达。虽然很明显MRAP是MC2R功能所必需的,但MRAP的作用机制才刚刚开始被理解。最近的研究已经开始揭示其中一些机制以及参与MC2R功能表达的MRAP结构域,并且新数据表明MRAP和MRAP2在其他黑皮质素受体的调控中都具有潜在作用。