细胞生物学
自噬
化学
降级(电信)
计算生物学
细胞
蛋白质降解
生物
可视化
蛋白质-蛋白质相互作用
程序性细胞死亡
血浆蛋白结合
领域(数学分析)
细胞凋亡
细胞生长
靶蛋白
蛋白质稳定性
HEK 293细胞
蛋白质结构域
焊剂(冶金)
纳米技术
作者
Keke Zhang,Ji Cheng,Jing‐Yi Zhang,Li‐Juan Tang,Fenglin Wang,Xia Chu,Jian‐Hui Jiang
摘要
Macroautophagy is central to cellular homeostasis and emerges as a promising avenue for targeted degradation. However, there is still a lack of efficient approaches allowing for visualizing macroautophagic flux and degradation. Here we develop a semi-synthetic LC3-interacting degrader (SLID) that enables fluorogenic imaging of macroautophagic activities and visualization of targeted degradation. SLID is engineered by fusing LC3-interacting regions (LIRs) to a self-labeling tag and an oligomeric motif, with the LIRs for binding to autophagosomes, the oligomeric motif for enhancing the binding, and the self-labeling tag for visualizing autophagosome formation using a pH indicator. SLID is further coupled to an antibody domain through a dimerization-induced proximity system, allowing chemically inducible degradation of target proteins. We show that this SLID platform permits efficient degradation of diverse target proteins such as disease-associated aggregation-prone proteins and phase-separated condensates. SLID also reveals elevated macroautophagic activities in senescent cells, and is repurposed for inducing senescent cell apoptosis via degradation of pro-survival and anti-apoptotic proteins. Our study highlights the great promise of SLID as a versatile tool for studying macroautophagy and targeted protein degradation.
科研通智能强力驱动
Strongly Powered by AbleSci AI