相互作用体
非共价相互作用
化学
串扰
生物素化
计算生物学
生物化学
共价键
仿形(计算机编程)
蛋白质-蛋白质相互作用
对接(动物)
代谢物
血浆蛋白结合
生物
免疫系统
代谢途径
胞浆
细胞生物学
化学生物学
免疫沉淀
共价结合
代谢稳定性
结合位点
小分子
酶
生物物理学
质量细胞仪
作者
Yunzhu Meng,Chenlin Zhang,Ao Yu,Yuan Liu,Chu Wang
标识
DOI:10.1021/acschembio.6c00419
摘要
Itaconate (ITA) is an immunoregulatory metabolite that is significantly upregulated in macrophages during bacterial infection. It can mediate immune and metabolic responses through both covalent modifications and noncovalent interactions with key proteins. While covalent itaconation has been systematically mapped using chemical probes, the global landscape of noncovalent targets of itaconate remains poorly explored. Here, we applied the peptide-centric local stability assay (PELSA) to globally profile the interactome of ITA in macrophage lysates. PELSA successfully identified known ITA targets and assigned ITA-responsive regions that correspond to authentic binding pockets. Comparative profiling with a structurally similar metabolite, α-ketoglutarate (AKG), further revealed the functional crosstalk between the two ligands. We biochemically validated the cytosolic isocitrate dehydrogenase 1 (IDH1) as a target of ITA, in which noncovalent interaction played a critical functional role. This study provides a valuable resource and underscores the importance of metabolic crosstalk between ITA and AKG.
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