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A激酶锚定蛋白:从结构到功能

AKAPs: from structure to function.

作者信息

Colledge M, Scott J D

机构信息

Howard Hughes Medical Institute, L-474, Vollum Institute, Oregon Health Sciences University, 3181 SW Sam Jackson Park Road, Portland, OR 97201, USA.

出版信息

Trends Cell Biol. 1999 Jun;9(6):216-21. doi: 10.1016/s0962-8924(99)01558-5.

Abstract

Compartmentalization of signalling molecules through association with anchoring proteins ensures specificity in signal transduction by placing enzymes close to their appropriate effectors and substrates. For example, 'A-kinase anchoring proteins' (AKAPs) bind to the regulatory subunit of cAMP-dependent protein kinase (PKA) to direct the kinase to discrete intracellular locations. Recently, functional studies aimed at disrupting AKAP-PKA complexes have demonstrated a role for anchored PKA in various cellular processes, including gene transcription, hormone-mediated insulin secretion and ion-channel modulation. By binding to additional signalling molecules, AKAPs might function to coordinate multiple components of signal-transduction pathways.

摘要

通过与锚定蛋白结合实现信号分子的区室化,可将酶置于其合适的效应器和底物附近,从而确保信号转导的特异性。例如,“A激酶锚定蛋白”(AKAPs)与环磷酸腺苷依赖性蛋白激酶(PKA)的调节亚基结合,将该激酶导向细胞内特定位置。最近,旨在破坏AKAP-PKA复合物的功能研究表明,锚定的PKA在多种细胞过程中发挥作用,包括基因转录、激素介导的胰岛素分泌和离子通道调节。通过与其他信号分子结合,AKAPs可能起到协调信号转导通路多个组分的作用。

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