Hundsrucker C, Rosenthal W, Klussmann E
Leibniz-Institut für Molekulare Pharmakologie, Campus Berlin-Buch, Robert-Rössle-Strasse 10, D-13125 Berlin, Germany.
Biochem Soc Trans. 2006 Aug;34(Pt 4):472-3. doi: 10.1042/BST0340472.
Adaptor or scaffolding proteins are at the basis of multiprotein complexes that spatially and temporally co-ordinate the propagation and integration of a broad range of cellular events. One class of scaffolding proteins are AKAPs (A-kinase-anchoring proteins). They sequester PKA (protein kinase A) and other signalling molecules including phosphodiesterases, other protein kinases and protein phosphatases to specific subcellular compartments. AKAP-dependent protein-protein interactions play a role in many physiologically relevant processes. For example, AKAP-PKA interactions are essential for the vasopressin-mediated water re-absorption in renal collecting duct principal cells or beta-adrenoceptor-induced increases in cardiac myocyte contractility. Here, we discuss recently developed peptide disruptors of AKAP-PKA interactions. Such peptides are valuable tools to study the relevance of PKA anchoring in cellular processes.
衔接蛋白或支架蛋白是多蛋白复合物的基础,这些复合物在空间和时间上协调广泛细胞事件的传播和整合。一类支架蛋白是A激酶锚定蛋白(AKAPs)。它们将蛋白激酶A(PKA)和其他信号分子(包括磷酸二酯酶、其他蛋白激酶和蛋白磷酸酶)隔离到特定的亚细胞区室。依赖AKAP的蛋白质-蛋白质相互作用在许多生理相关过程中发挥作用。例如,AKAP-PKA相互作用对于血管加压素介导的肾集合管主细胞中水的重吸收或β-肾上腺素能受体诱导的心肌细胞收缩力增加至关重要。在这里,我们讨论了最近开发的AKAP-PKA相互作用的肽干扰剂。此类肽是研究PKA锚定在细胞过程中的相关性的有价值工具。