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The untapped potential of tyrosine-based G protein signaling

机译:基于酪氨酸的G蛋白信号的未开发潜力

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摘要

Tyrosine-based and trimeric G protein-based signaling are the two most widely studied and distinct mechanisms for signal transduction in eukaryotes. How each of them relay signals across the plasma membrane independently of each other has been extensively characterized; however, an understanding of how they work together remained obscure. Recently, a rapidly emerging paradigm has revealed that tyrosine based signals are relayed via G proteins, and that the cross-talk between the two hubs are more robustly and sophisticatedly integrated than was previously imagined. More importantly, by straddling the two signaling hubs that are most frequently targeted for their therapeutic significance, the tyrosine based G-protein signaling pathway has its own growing list of pathophysiologic importance, both as therapeutic target in a variety of disease states, and by paving the way for personalized medicine. The fundamental principles of this emerging paradigm and its pharmacologic potential are discussed. (C) 2016 Elsevier Ltd. All rights reserved.
机译:基于酪氨酸和三聚体G蛋白的信号传导是真核生物中信号转导的两种研究最广泛且截然不同的机制。它们中的每一个如何彼此独立地在质膜上传递信号已被广泛地表征。但是,对于它们如何一起工作的理解仍然很模糊。最近,一个迅速出现的范例表明,基于酪氨酸的信号是通过G蛋白传递的,并且两个集线器之间的串扰比以前想象的更牢固,更复杂。更重要的是,基于酪氨酸的G蛋白信号转导通路跨越了两个因治疗意义而最常被靶向的信号转导枢纽,其自身的病理生理学重要性列表不断增加,既可作为多种疾病状态下的治疗靶标,又可以铺路个性化医学的方式。讨论了这种新兴范式的基本原理及其药理潜力。 (C)2016 Elsevier Ltd.保留所有权利。

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