Sexton P M, Albiston A, Morfis M, Tilakaratne N
Molecular Pharmacology Laboratory, Department of Pharmacology, The University of Melbourne, Victoria 3010, Australia.
Cell Signal. 2001 Feb;13(2):73-83. doi: 10.1016/s0898-6568(00)00143-1.
Our understanding of G protein-coupled receptor (GPCR) function has recently expanded to encompass novel protein interactions that underlie both cell-surface receptor expression and the exhibited phenotype. The most notable examples are those involving receptor activity modifying proteins (RAMPs). RAMP association with the calcitonin (CT) receptor-like receptor (CRLR) traffics this receptor to the cell surface where individual RAMPs dictate the expression of unique phenotypes. A similar function has been ascribed to RAMP interaction with the CT receptor (CTR) gene product. This review examines our current state of knowledge of the mechanisms underlying RAMP function.
我们对G蛋白偶联受体(GPCR)功能的理解最近有所扩展,涵盖了细胞表面受体表达和所表现出的表型背后的新型蛋白质相互作用。最显著的例子是那些涉及受体活性调节蛋白(RAMP)的相互作用。RAMP与降钙素(CT)受体样受体(CRLR)的结合将该受体转运至细胞表面,在那里单个RAMP决定独特表型的表达。RAMP与CT受体(CTR)基因产物的相互作用也被认为具有类似功能。本综述探讨了我们目前对RAMP功能潜在机制的了解情况。