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通过生物正交探针在炎症巨噬细胞中对衣康酸的化学蛋白质组学分析。

Chemoproteomic Profiling of Itaconation by Bioorthogonal Probes in Inflammatory Macrophages.

出版信息

J Am Chem Soc. 2020 Jun 24;142(25):10894-10898. doi: 10.1021/jacs.9b11962. Epub 2020 Jun 11.

Abstract

Itaconate is an anti-inflammatory metabolite involved in pathogen-macrophage interactions, but the mechanisms underlying its effect are not fully understood. Competitive cysteine profiling has been performed to interrogate itaconate's reactivity in cell lysates, but methods for analyzing targets of itaconation directly in living macrophages are still lacking. In this work, we developed a specific bioorthogonal probe, itaconate-alkyne (ITalk), for quantitative and site-specific chemoproteomic profiling of itaconation in inflammatory macrophages. ITalk recapitulates the anti-inflammatory property of itaconate and enables biochemical evaluation and proteomic analysis of its direct targets. Our study delineates the widespread landscape of itaconate substrates, providing a versatile tool and comprehensive resource for investigating its function.

摘要

衣康酸是一种参与病原体与巨噬细胞相互作用的抗炎代谢物,但它的作用机制尚未完全了解。已经进行了竞争性半胱氨酸分析,以探究衣康酸在细胞裂解物中的反应性,但在活巨噬细胞中直接分析衣康酸盐化的靶标的方法仍然缺乏。在这项工作中,我们开发了一种特异性的生物正交探针,衣康酸-炔(ITalk),用于定量和特异性化学蛋白质组学分析炎症巨噬细胞中的衣康酸盐化。ITalk 重现了衣康酸的抗炎特性,并能够对其直接靶标的生化评估和蛋白质组学分析。我们的研究描绘了衣康酸底物的广泛景观,为研究其功能提供了一种通用的工具和全面的资源。

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