摘要

beta-arrestin 1 and 2 (also known as arrestin 2 and 3) are homologous adaptor proteins that regulate seven-transmembrane receptor trafficking and signalling. Other proteins with predicted 'arrestin-like' structural domains but lacking sequence homology have been indicated to function like beta-arrestin in receptor regulation. We demonstrate that beta-arrestin2 is the primary adaptor that rapidly binds agonist-activated beta(2) adrenergic receptors (beta(2)ARs) and promotes clathrin-dependent internalization, E3 ligase Nedd4 recruitment and ubiquitin-dependent lysosomal degradation of the receptor. The arrestin-domain-containing (ARRDC) proteins 2, 3 and 4 are secondary adaptors recruited to internalized beta(2)AR-Nedd4 complexes on endosomes and do not affect the adaptor roles of beta-arrestin2. Rather, the role of ARRDC proteins is to traffic Nedd4-beta(2)AR complexes to a subpopulation of early endosomes.

  • 出版日期2013-2