化学
细胞生物学
生物物理学
线粒体
生物化学
过氧化氢
生物素化
基质(化学分析)
活性氧
酶
5-羟甲基胞嘧啶
海马结构
氧化还原
过氧亚硝酸盐
纳米技术
链霉亲和素
基质金属蛋白酶
体内
计算机科学
氧化应激
KEAP1型
磷酸化
线粒体基质
细胞信号
生物
酿酒酵母
信号转导
计算生物学
氢
酵母
寡核苷酸
突变体
核糖核酸
作者
Boyi Chen,Hongyang Guo,Zhijian Yan,Wenjie Lu,Chun Li,Shuai Xu,Yanling Zhang,Haodong Guo,Shaopeng Sun,Xuege Sun,Shangxun Zhao,Qiaoling Shangguan,Yidong Chen,Lei Lü,Zhaofa Wu,Ying Chen,Wei Qin
出处
期刊:
[Cold Spring Harbor Laboratory]
日期:2026-03-15
被引量:2
标识
DOI:10.64898/2026.03.13.711744
摘要
Proximity labeling (PL) technologies like APEX2 have transformed spatial multi-omics in live cells, but their long-standing dependence on hydrogen peroxide (H₂O₂) disrupts redox signaling and prevents use in live animals. Here we introduce H₂O₂-independent APEX2 (Hi-APEX), which uses a clickable tetrazine-phenol probe, requiring no enzyme engineering. We show that APEX2 directly catalyzes TP radical formation without H₂O₂ via a mechanism requiring the probe’s tetrazine group and a key histidine residue. We benchmarked Hi-APEX-based spatial multi-omics by mapping the mitochondrial matrix and dynamic secretomes. Hi-APEX significantly outperforms traditional APEX in capturing redox-sensitive processes such as stress response and ferroptosis, enabling discovering authentic stress granule components and protein interaction networks for mitochondria-localized GPx4. One mGPx4 interactor TRMT61B—known to regulate mitochondrial m¹A modifications—promotes ferroptosis. Crucially, Hi-APEX achieves full in vivo compatibility, enabling direct PL in tumor xenografts and hippocampal neurons, thereby expanding PL-based spatial multi-omics from cellular systems to living organisms.
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