Dessauer Carmen W
Department of Integrative Biology and Pharmacology, University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
Mol Pharmacol. 2009 Nov;76(5):935-41. doi: 10.1124/mol.109.059345. Epub 2009 Aug 14.
The formation of multiprotein complexes is a repeated theme in biology ranging from the regulation of the extracellular signal-regulated kinase and cAMP signaling pathways to the formation of postsynaptic density complexes or tight junctions. A-kinase anchoring proteins (AKAPs) are well known for their ability to scaffold protein kinase A and components upstream and downstream of cAMP production, including G protein-coupled receptors, cAMP-dependent Rap-exchange factors, and phosphodiesterases. Specific adenylyl cyclase (AC) isoforms have also been identified as components of AKAP complexes, namely AKAP79, Yotiao, and mAKAP. In this review, we summarize recent evidence for AC-AKAP complexes and requirements for compartmentalization of cAMP signaling. The ability of AKAPs to assemble intricate feedback loops to control spatiotemporal aspects of cAMP signaling adds yet another dimension to the classic cAMP pathway.
多蛋白复合物的形成是生物学中的一个常见主题,涵盖从细胞外信号调节激酶和cAMP信号通路的调节到突触后致密复合物或紧密连接的形成。A激酶锚定蛋白(AKAPs)以其能够搭建蛋白激酶A以及cAMP产生上游和下游成分(包括G蛋白偶联受体、cAMP依赖性Rap交换因子和磷酸二酯酶)的支架而闻名。特定的腺苷酸环化酶(AC)同工型也已被鉴定为AKAP复合物的成分,即AKAP79、Yotiao和mAKAP。在本综述中,我们总结了AC-AKAP复合物的最新证据以及cAMP信号分隔的要求。AKAP组装复杂反馈回路以控制cAMP信号时空方面的能力为经典的cAMP途径增添了另一个维度。