Casar Berta, Crespo Piero
Instituto de Biomedicina y Biotecnología de Cantabria, Consejo Superior de Investigaciones Científicas (CSIC) - Universidad de Cantabria Santander, Spain.
Front Cell Dev Biol. 2016 May 31;4:49. doi: 10.3389/fcell.2016.00049. eCollection 2016.
ERK1/2 MAP Kinases become activated in response to multiple intra- and extra-cellular stimuli through a signaling module composed of sequential tiers of cytoplasmic kinases. Scaffold proteins regulate ERK signals by connecting the different components of the module into a multi-enzymatic complex by which signal amplitude and duration are fine-tuned, and also provide signal fidelity by isolating this complex from external interferences. In addition, scaffold proteins play a central role as spatial regulators of ERKs signals. In this respect, depending on the subcellular localization from which the activating signals emanate, defined scaffolds specify which substrates are amenable to be phosphorylated. Recent evidence has unveiled direct interactions among different scaffold protein species. These scaffold-scaffold macro-complexes could constitute an additional level of regulation for ERK signals and may serve as nodes for the integration of incoming signals and the subsequent diversification of the outgoing signals with respect to substrate engagement.
ERK1/2丝裂原活化蛋白激酶通过由细胞质激酶的连续层级组成的信号模块,对多种细胞内和细胞外刺激做出反应而被激活。支架蛋白通过将模块的不同组件连接成一个多酶复合物来调节ERK信号,通过该复合物可微调信号幅度和持续时间,并且还通过将该复合物与外部干扰隔离来提供信号保真度。此外,支架蛋白作为ERK信号的空间调节剂发挥核心作用。在这方面,根据激活信号发出的亚细胞定位,特定的支架蛋白决定了哪些底物易于被磷酸化。最近的证据揭示了不同支架蛋白种类之间的直接相互作用。这些支架-支架大复合物可能构成ERK信号的额外调节水平,并可能作为整合传入信号以及随后关于底物参与的传出信号多样化的节点。