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磷酸化后的 Pin1 催化构象调节:细胞信号转导和药物发现中的独特检查点。

Pin1-catalyzed conformational regulation after phosphorylation: A distinct checkpoint in cell signaling and drug discovery.

机构信息

Departments of Biochemistry and Oncology, Schulich School of Medicine & Dentistry, Western University, London, ON N6G 2V4, Canada.

Robarts Research Institute, Schulich School of Medicine & Dentistry, Western University, London, ON N6G 2V4, Canada.

出版信息

Sci Signal. 2024 Jun 18;17(841):eadi8743. doi: 10.1126/scisignal.adi8743.

Abstract

Protein phosphorylation is one of the most common mechanisms regulating cellular signaling pathways, and many kinases and phosphatases are proven drug targets. Upon phosphorylation, protein functions can be further regulated by the distinct isomerase Pin1 through cis-trans isomerization. Numerous protein targets and many important roles have now been elucidated for Pin1. However, no tools are available to detect or target cis and trans conformation events in cells. The development of Pin1 inhibitors and stereo- and phospho-specific antibodies has revealed that cis and trans conformations have distinct and often opposing cellular functions. Aberrant conformational changes due to the dysregulation of Pin1 can drive pathogenesis but can be effectively targeted in age-related diseases, including cancers and neurodegenerative disorders. Here, we review advances in understanding the roles of Pin1 signaling in health and disease and highlight conformational regulation as a distinct signal transduction checkpoint in disease development and treatment.

摘要

蛋白质磷酸化是调节细胞信号通路的最常见机制之一,许多激酶和磷酸酶已被证实是药物靶点。磷酸化后,蛋白质的功能可以通过 Pin1 的顺反异构酶进一步调节。现在已经阐明了 Pin1 的许多蛋白质靶标和许多重要作用。然而,目前还没有工具可用于检测或靶向细胞中的顺式和反式构象事件。Pin1 抑制剂和立体和磷酸特异性抗体的开发表明,顺式和反式构象具有不同且通常相反的细胞功能。由于 Pin1 的失调导致的构象变化会引发疾病,但在与年龄相关的疾病(包括癌症和神经退行性疾病)中可以有效地靶向这些变化。在这里,我们综述了对 Pin1 信号在健康和疾病中的作用的理解进展,并强调构象调节作为疾病发展和治疗中的一个独特的信号转导检查点。

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