胞浆
化学
生物化学
化学生物学
TFAM公司
线粒体
毒性
马兜铃酸
热稳定性
蛋白质降解
泛素
DNA损伤
生物
DNA
炎症
氨基酸
细胞生物学
蛋白质组学
肾
阻抑素
热休克蛋白90
蛋白质生物合成
连接器
核糖体
作者
Yin Gong,Shanshan Zhang,Anying Wei,Xiang Ji,Xiaodan Chong,Jinfeng Cen,Xuan Zhao,Zimeng Luo,Zhipeng Pei,Guanchao Mao,Xinkang Zhang,Mingxue Sun,Zhiguo Sun,Zifei Yin,Zhengrong Zou,Wenqi Meng
标识
DOI:10.1002/advs.202513117
摘要
Exposure to aristolochic acids (AA) via the ingestion of AA-containing medicine or food is a significant risk factor for severe nephropathy. Despite decades of research, the direct molecular targets underlying AA toxicity remain elusive. In this study, a map of the AA-binding protein atlas in kidney tissues is constructed via the design and synthesis of an AA-based affinity probe. Among the AA-binding proteins, HIGD1A is identified as a high-affinity AA target (SPR: 59.6 nm; ITC: 195 nm) with significant thermostability changes upon AA binding. Furthermore, AA disrupted the HIGD1A-TFAM interaction, triggering TFAM degradation via the autophagy-lysosome pathway. This led to the accumulation of cytosolic mitochondrial DNA. This study also suggested that HIGD1A also contributed to AA-induced inflammation by increasing the cytosolic levels of oxidized mitochondrial DNA to activate the MAPK and NF-κB pathways. This study not only reveals an important target protein of AA but also provides novel inspiration and ideas for toxicology and chemical biology research.
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