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通过靶向 TM V-TMVI 结构域来实现 CXCR4:CXCL12 轴的变构调节,从而实现受体纳米簇的靶向。

Allosteric modulation of the CXCR4:CXCL12 axis by targeting receptor nanoclustering via the TMV-TMVI domain.

机构信息

Chemokine Signaling group, Department of Immunology and Oncology, Centro Nacional de Biotecnología/CSIC, Campus de Cantoblanco, Madrid, Spain.

Division of Diagnostics and Specialist Medicine, Department of Health, Medical and Caring Sciences, Linköping University, Linköping, Sweden.

出版信息

Elife. 2024 Sep 9;13:RP93968. doi: 10.7554/eLife.93968.

Abstract

CXCR4 is a ubiquitously expressed chemokine receptor that regulates leukocyte trafficking and arrest in both homeostatic and pathological states. It also participates in organogenesis, HIV-1 infection, and tumor development. Despite the potential therapeutic benefit of CXCR4 antagonists, only one, plerixafor (AMD3100), which blocks the ligand-binding site, has reached the clinic. Recent advances in imaging and biophysical techniques have provided a richer understanding of the membrane organization and dynamics of this receptor. Activation of CXCR4 by CXCL12 reduces the number of CXCR4 monomers/dimers at the cell membrane and increases the formation of large nanoclusters, which are largely immobile and are required for correct cell orientation to chemoattractant gradients. Mechanistically, CXCR4 activation involves a structural motif defined by residues in TMV and TMVI. Using this structural motif as a template, we performed in silico molecular modeling followed by in vitro screening of a small compound library to identify negative allosteric modulators of CXCR4 that do not affect CXCL12 binding. We identified AGR1.137, a small molecule that abolishes CXCL12-mediated receptor nanoclustering and dynamics and blocks the ability of cells to sense CXCL12 gradients both in vitro and in vivo while preserving ligand binding and receptor internalization.

摘要

趋化因子受体 4(CXCR4)是一种广泛表达的趋化因子受体,调节白细胞在稳态和病理状态下的迁移和停留。它还参与器官发生、HIV-1 感染和肿瘤发展。尽管 CXCR4 拮抗剂具有潜在的治疗益处,但只有一种,即阻断配体结合位点的plerixafor(AMD3100),已进入临床。成像和生物物理技术的最新进展提供了对该受体的膜组织和动力学的更深入理解。CXCL12 激活 CXCR4 会减少细胞膜上的 CXCR4 单体/二聚体数量,并增加大纳米簇的形成,这些纳米簇大部分是不可动的,并且对于正确的细胞定向到趋化因子梯度是必需的。从机制上讲,CXCR4 的激活涉及由 TMV 和 TMVI 中的残基定义的结构基序。我们使用该结构基序作为模板进行计算机分子建模,然后对小分子文库进行体外筛选,以鉴定不影响 CXCL12 结合的 CXCR4 的负变构调节剂。我们鉴定出 AGR1.137 是一种小分子,它可以消除 CXCL12 介导的受体纳米簇形成和动力学,并阻止细胞在体外和体内感知 CXCL12 梯度的能力,同时保留配体结合和受体内化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82df/11383527/f6da98e555a1/elife-93968-fig1.jpg

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