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解析细胞因子信号抑制蛋白家族蛋白的可药用性及免疫作用

Unravelling the druggability and immunological roles of the SOCS-family proteins.

作者信息

Lynch Dylan M, Forrester Beth, Webb Thomas, Ciulli Alessio

机构信息

Centre for Targeted Protein Degradation, Division of Biological Chemistry and Drug Discovery, School of Life Sciences, University of Dundee, Dundee, United Kingdom.

出版信息

Front Immunol. 2024 Nov 29;15:1449397. doi: 10.3389/fimmu.2024.1449397. eCollection 2024.

DOI:10.3389/fimmu.2024.1449397
PMID:39676878
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11638205/
Abstract

The Suppressor of Cytokine Signalling (SOCS) protein family play a critical role in cytokine signalling and regulation of the JAK/STAT pathway with functional consequences to the immune response. Members of this family are implicated in multiple different signalling cascades that drive autoimmune diseases and cancer, through their binding to phosphotyrosine modified proteins as well as ubiquitination activity as part of Cullin5 RING E3 ligases. Here we review the SOCS family members CISH and SOCS1-SOCS7, with a focus on their complex role in immunity. The interactome and signalling network of this protein family is discussed, and the intricate mechanisms through which SOCS proteins alter and manage the immune system are assessed. We offer structural insights into how SOCS proteins engage their interacting partners and native substrates at the protein-protein interaction level. We describe how this knowledge has enabled drug discovery efforts on SOCS proteins to date and propose strategies for therapeutic intervention using small molecules, either via direct inhibition or leveraging their E3 ligase activity for targeted protein degradation.

摘要

细胞因子信号转导抑制因子(SOCS)蛋白家族在细胞因子信号转导以及JAK/STAT通路的调控中发挥关键作用,对免疫反应具有功能性影响。该家族成员通过与磷酸酪氨酸修饰蛋白结合以及作为Cullin5 RING E3连接酶的一部分进行泛素化活性,参与多种不同的信号级联反应,这些反应驱动自身免疫性疾病和癌症的发生。在此,我们综述SOCS家族成员CISH和SOCS1 - SOCS7,重点关注它们在免疫中的复杂作用。讨论了该蛋白家族的相互作用组和信号网络,并评估了SOCS蛋白改变和调控免疫系统的复杂机制。我们从蛋白质 - 蛋白质相互作用层面,提供了关于SOCS蛋白如何与它们的相互作用伙伴和天然底物结合的结构见解。我们描述了迄今为止基于这些知识在SOCS蛋白上开展的药物研发工作,并提出了使用小分子进行治疗干预的策略,包括直接抑制或利用其E3连接酶活性进行靶向蛋白降解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ba/11638205/8550ec3c309e/fimmu-15-1449397-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ba/11638205/aec6dcf910d0/fimmu-15-1449397-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ba/11638205/0f82448c9260/fimmu-15-1449397-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ba/11638205/ee5458fd767f/fimmu-15-1449397-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ba/11638205/2d804efb39a7/fimmu-15-1449397-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ba/11638205/9901e26b4b21/fimmu-15-1449397-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ba/11638205/8550ec3c309e/fimmu-15-1449397-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ba/11638205/aec6dcf910d0/fimmu-15-1449397-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ba/11638205/fac8ecca1b03/fimmu-15-1449397-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ba/11638205/0f82448c9260/fimmu-15-1449397-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ba/11638205/d2fec4551a9c/fimmu-15-1449397-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ba/11638205/ee5458fd767f/fimmu-15-1449397-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ba/11638205/2d804efb39a7/fimmu-15-1449397-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ba/11638205/9901e26b4b21/fimmu-15-1449397-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ba/11638205/8550ec3c309e/fimmu-15-1449397-g008.jpg

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2
knockout mice exhibit similar outcomes to malaria infection despite altered hematopoietic responses.基因敲除小鼠尽管造血反应发生了改变,但对疟疾感染表现出相似的结果。
Front Microbiol. 2023 Nov 2;14:1288876. doi: 10.3389/fmicb.2023.1288876. eCollection 2023.
3
SOCS-JAK-STAT inhibitors and SOCS mimetics as treatment options for autoimmune uveitis, psoriasis, lupus, and autoimmune encephalitis.
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Am J Transl Res. 2025 Mar 15;17(3):1780-1791. doi: 10.62347/VIVI6495. eCollection 2025.
SOCS-JAK-STAT 抑制剂和 SOCS 模拟物作为治疗自身免疫性葡萄膜炎、银屑病、狼疮和自身免疫性脑炎的选择。
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Structure-based design of a phosphotyrosine-masked covalent ligand targeting the E3 ligase SOCS2.基于结构设计靶向E3连接酶SOCS2的磷酸酪氨酸屏蔽共价配体
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