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用多功能细胞内变构探针标记 CC 趋化因子受体 2。

Labeling of CC Chemokine Receptor 2 with a Versatile Intracellular Allosteric Probe.

机构信息

Leiden Academic Centre for Drug Research, Division of Medicinal Chemistry, Leiden 2333 CC, The Netherlands.

出版信息

ACS Chem Biol. 2024 Sep 20;19(9):2070-2080. doi: 10.1021/acschembio.4c00439. Epub 2024 Aug 26.

DOI:10.1021/acschembio.4c00439
PMID:39186040
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11420878/
Abstract

Interest in affinity-based probes (AfBPs) as novel tools to interrogate G protein-coupled receptors (GPCRs) has gained traction in recent years. AfBPs represent an interesting and more versatile alternative to antibodies. In the present study, we report the development and validation of AfBPs that target the intracellular allosteric pocket of CCR2, a GPCR of interest for the development of therapies targeting autoimmune and inflammatory diseases and also cancer. Owing to the two-step labeling process of these CCR2 AfBPs through the incorporation of a click handle, we were successful in applying our most efficient probe in a variety of experiments and making use of multiple different detection techniques, such as SDS-PAGE and LC/MS-based proteomics. Collectively, this novel probe shows high selectivity, versatility, and applicability. Hence, this is a valuable alternative for CCR2-targeting antibodies and other traditional tool compounds and could aid in target validation and engagement in drug discovery.

摘要

近年来,人们对基于亲和力的探针(AfBPs)作为研究 G 蛋白偶联受体(GPCRs)的新型工具产生了浓厚的兴趣。AfBPs 是一种有趣且更具多功能性的抗体替代物。在本研究中,我们报告了针对 CCR2 细胞内变构口袋的 AfBPs 的开发和验证,CCR2 是一种 GPCR,对于开发针对自身免疫和炎症性疾病以及癌症的治疗方法具有重要意义。由于通过引入点击手柄对这些 CCR2 AfBPs 进行两步标记过程,我们成功地在各种实验中应用了我们最有效的探针,并利用了多种不同的检测技术,如 SDS-PAGE 和基于 LC/MS 的蛋白质组学。总的来说,这种新型探针具有高选择性、多功能性和适用性。因此,它是 CCR2 靶向抗体和其他传统工具化合物的有价值的替代品,并可用于靶标验证和药物发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8bc/11420878/8b8fadad1b31/cb4c00439_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8bc/11420878/b333dfc37c0d/cb4c00439_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8bc/11420878/5d6a46a4e23c/cb4c00439_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8bc/11420878/df0abf11614f/cb4c00439_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8bc/11420878/e91211b3e732/cb4c00439_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8bc/11420878/dc9a9887af55/cb4c00439_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8bc/11420878/8b8fadad1b31/cb4c00439_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8bc/11420878/b333dfc37c0d/cb4c00439_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8bc/11420878/5d6a46a4e23c/cb4c00439_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8bc/11420878/df0abf11614f/cb4c00439_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8bc/11420878/e91211b3e732/cb4c00439_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8bc/11420878/dc9a9887af55/cb4c00439_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8bc/11420878/8b8fadad1b31/cb4c00439_0005.jpg

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