化学
胞外囊泡
免疫系统
细胞外
核糖核酸
细胞生物学
跟踪(教育)
计算生物学
微泡
生物化学
基因
遗传学
心理学
小RNA
教育学
生物
作者
Zheng Zhang,Zhuojun Luo,Yikai Liu,Subhransu S. Sahoo,Vamara Dembele,Meng‐Ju Wu,Nabeel Bardeesy,Fang Huang,Majid Kazemian,Kyle A. Cottrell,W. Andy Tao
摘要
RNA cargos in extracellular vesicles (EVs) mediate intercellular communication by engaging RNA-binding proteins (RBPs) in recipient cells. Here, we introduce extracellular RNA interactome capture through orthogonal labelings (ERICOL), a targeted cross-linking and quantitative chemical proteomic strategy based on metabolic labeling of RNAs and stable isotope labeling of proteins for systematic profiling of EV RBPs in recipient cells. Time-resolved analysis of tumor-derived EVs in Jurkat T cells revealed dynamic patterns of EV RNA uptake and RBP engagement. Further profiling in primary human CD8+ T cells treated with wild-type or IDH1 mutant intrahepatic cholangiocarcinoma (ICC)-derived EVs uncovered IDH1 mutation-driven alterations in the EV RBP landscape. ERICOL offers a powerful strategy for comprehensive profiling of EV RNA interactome dynamics and provides mechanistic insights into EV-mediated immune modulation.
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