Exploring Diverse Signaling Mechanisms of G Protein-Coupled Receptors through Structural Biology.

IF 2.1 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of biochemistry Pub Date : 2024-03-25 DOI:10.1093/jb/mvae018
Ryoji Suno
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Abstract

Recent advancements in structural biology have facilitated the elucidation of complexes involving G protein-coupled receptors (GPCRs) and their associated signal transducers, including G proteins and arrestins. A comprehensive analysis of these structures provides profound insights into the dynamics of signaling mechanisms. These structural revelations can potentially guide the development of drugs to minimize side effects through targeted and selective signaling. Understanding the binding modes of different signal-selective ligands is imperative for future drug research and development. Here, we conduct a comparative examination of the structural details of various GPCR-signal transducer complexes and delve into the molecular basis of the currently proposed signal selectivity.

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通过结构生物学探索 G 蛋白偶联受体的多种信号机制。
结构生物学的最新进展有助于阐明涉及 G 蛋白偶联受体(GPCR)及其相关信号转导物(包括 G 蛋白和抑制蛋白)的复合物。通过对这些结构的全面分析,可以深入了解信号传递机制的动态。这些结构上的启示有可能为药物开发提供指导,通过有针对性和选择性的信号传导将副作用降到最低。了解不同信号选择性配体的结合模式对于未来的药物研究和开发至关重要。在此,我们对各种 GPCR 信号转导复合物的结构细节进行了比较研究,并深入探讨了目前提出的信号选择性的分子基础。
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来源期刊
Journal of biochemistry
Journal of biochemistry 生物-生化与分子生物学
CiteScore
4.80
自引率
3.70%
发文量
101
审稿时长
4-8 weeks
期刊介绍: The Journal of Biochemistry founded in 1922 publishes the results of original research in the fields of Biochemistry, Molecular Biology, Cell, and Biotechnology written in English in the form of Regular Papers or Rapid Communications. A Rapid Communication is not a preliminary note, but it is, though brief, a complete and final publication. The materials described in Rapid Communications should not be included in a later paper. The Journal also publishes short reviews (JB Review) and papers solicited by the Editorial Board.
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