细胞内
蛋白酶体
蛋白质降解
细胞生物学
胞浆
降级(电信)
化学
克拉斯
泛素
HEK 293细胞
转运蛋白
生物
细胞
计算生物学
蛋白质-蛋白质相互作用
血浆蛋白结合
内生
酿酒酵母
蛋白质稳定性
生物化学
酵母
生物物理学
蛋白质水解
靶蛋白
作者
Y Li,Zhicheng Jin,Sharif U. Ahmed,Jagotamoy Das,Reiner Bleher,Dingran Chang,Xiaozhou Yu,Connor D. Flynn,Jiajing Zhou,Xiaobing Hu,Kangfu Chen,Kimberly T. Riordan,Ranjit Atwal,Julia M. Mayes,Zongjie Wang,Shana O. Kelley
标识
DOI:10.1038/s41467-026-72967-8
摘要
Targeted protein degradation harnesses endogenous cellular machinery to eliminate disease-causing proteins, yet achieving phenotype-specific degradation across diverse cell types remains challenging. Here we show that antibody-enriched biomolecular condensates formed by liquid–liquid phase separation function as intracellular protein degradation tools, combining cytosolic trafficking with direct proteasome recruitment for targeted substrate clearance. These nanoscale condensates incorporate a short proteasome-targeting motif into phase-separation precursors, preserve antibody activity, enable direct proteasome recruitment, and improve delivery uniformity. When loaded with a mutation-specific antibody, these condensates selectively degrade oncogenic KRAS G12V without affecting wild-type KRAS in heterozygous cells, and suppress tumor growth in a KRAS G12V xenograft model. This strategy provides a modular platform for intracellular protein degradation that can be readily adapted by exchanging antibodies, without requiring genetic modification of cellular system. Targeted protein degradation has huge potential, but phenotype-specific degradation remains a difficulty. Here, a phase-separation biomolecular condensates as an intracellular degradation agent is developed, combining antibody-guided recognition with direct proteasome recruitment to enable phenotype-selective protein clearance.
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