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趋化因子受体 N 端电荷决定了对翻译后修饰的依赖,以有效捕获配体,并随后被防御肽增强。

Chemokine Receptor N-Terminus Charge Dictates Reliance on Post-Translational Modifications for Effective Ligand Capture and Following Boosting by Defense Peptides.

机构信息

Department of Biomedical Sciences, University of Copenhagen, 2200 Copenhagen, Denmark.

Copenhagen Center for Glycomics, University of Copenhagen, 2200 Copenhagen, Denmark.

出版信息

Int J Mol Sci. 2024 Oct 9;25(19):10854. doi: 10.3390/ijms251910854.

Abstract

The chemokine receptors CCR1 and CCR5 display overlapping expression patterns and ligand dependency. Here we find that ligand activation of CCR5, not CCR1, is dependent on N-terminal receptor O-glycosylation. Release from O-glycosylation dependency is obtained by increasing CCR5 N-terminus acidity to the level of CCR1. Ligand activation of CCR5, not CCR1, drastically improves in the absence of glycosaminoglycans (GAGs). Ligand activity at both CCR1 and CCR5 is boosted by positively charged/basic peptides shown to interact with acidic chemokine receptor N-termini. We propose that receptors with an inherent low N-terminus acidity rely on post-translational modifications (PTMs) to efficiently compete with acidic entities in the local environment for ligand capture. Although crucial for initial ligand binding, strong electrostatic interactions between the ligand and the receptor N-terminus may counteract following insertion of the ligand into the receptor binding pocket and activation, a process that seems to be aided in the presence of basic peptides. Basic peptides bind to the naked CCR1 N-terminus, not the CCR5 N-terminus, explaining the loss of boosting of ligand-induced signaling via CCR5 in cells incapable of glycosylation.

摘要

趋化因子受体 CCR1 和 CCR5 表现出重叠的表达模式和配体依赖性。在这里,我们发现 CCR5 的配体激活依赖于 N 端受体 O-糖基化,而不是 CCR1。通过将 CCR5 N 端酸度提高到 CCR1 水平,可以获得对 O-糖基化依赖性的释放。在缺乏糖胺聚糖 (GAGs) 的情况下,CCR5 的配体激活而非 CCR1 的配体激活大大改善。显示与酸性趋化因子受体 N 端相互作用的带正电荷/碱性肽可增强 CCR1 和 CCR5 的配体活性。我们提出,具有固有低 N 端酸度的受体依赖于翻译后修饰 (PTM),以有效地与局部环境中的酸性实体竞争配体捕获。尽管对于初始配体结合至关重要,但配体与受体 N 端之间的强静电相互作用可能会阻碍配体插入受体结合口袋并激活,这一过程似乎在存在碱性肽的情况下得到帮助。碱性肽与裸露的 CCR1 N 端结合,而不是 CCR5 N 端结合,这解释了在不能糖基化的细胞中,通过 CCR5 诱导的信号转导失去增强的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a19a/11477141/2799ae64ca01/ijms-25-10854-g001.jpg

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