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首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >Conformational transitions and interactions underlying the function of membrane embedded receptor protein kinases
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Conformational transitions and interactions underlying the function of membrane embedded receptor protein kinases

机译:膜嵌入受体蛋白激酶功能的构象转变和相互作用

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Among membrane receptors, the single-span receptor protein kinases occupy a broad but specific functional niche determined by distinctive features of the underlying transmembrane signaling mechanisms that are briefly overviewed on the basis of some of the most representative examples, followed by a more detailed discussion of several hierarchical levels of organization and interactions involved. All these levels, including single-molecule interactions (e.g., dimerization, liganding, chemical modifications), local processes (e.g. lipid membrane perturbations, cytoskeletal interactions), and larger scale phenomena (e.g., effects of membrane surface shape or electrochemical potential gradients) appear to be closely integrated to achieve the observed diversity of the receptor functioning. Different species of receptor protein kinases meet their specific functional demands through different structural features defining their responses to stimulation, but certain common patterns exist. Signaling by receptor protein kinases is typically associated with the receptor dimerization and clustering, ligand-induced rearrangements of receptor domains through allosteric conformational transitions with involvement of lipids, release of the sequestered lipids, restriction of receptor diffusion, cytoskeleton and membrane shape remodeling. Understanding of complexity and continuity of the signaling processes can help identifying currently neglected opportunities for influencing the receptor signaling with potential therapeutic implications. This article is part of a Special Issue entitled: Interactions between membrane receptors in cellular membranes edited by Kalina Hristova. (C) 2017 Elsevier B.V. All rights reserved.
机译:在膜受体中,单跨度受体蛋白激酶占据通过基于一些最具代表性示例的潜在跨膜信号传导机制的独特特征而确定的宽但特异性的功能性,其次是更详细的讨论涉及的几个组织水平和互动。所有这些水平,包括单分子相互作用(例如,二聚,韧带,化学修饰),局部方法(例如脂质膜扰动,细胞骨架相互作用)和更大的尺度现象(例如,膜表面形状或电化学潜在梯度的影响)出现密切合并以实现观察到的受体功能的多样性。不同种类的受体蛋白激酶通过不同的结构特征来满足其特定的功能需求,这些特征定义它们对刺激的反应,但存在某些常见的模式。受体蛋白激酶的信号传导通常与受体二聚化和聚类,通过脂质累及的血糖构象转变,释放螯合脂质的释放,受体扩散,细胞骨架和膜形状重塑的限制。了解信号传导过程的复杂性和连续性可以有助于识别目前忽略了影响的受体信号,具有潜在的治疗意义。本文是标题的特殊问题的一部分:Kalina Hristova编辑细胞膜中膜受体之间的相互作用。 (c)2017 Elsevier B.v.保留所有权利。

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