应力颗粒
蛋白质组学
核糖核蛋白
细胞生物学
颗粒(地质)
化学
计算生物学
基因敲除
生物物理学
生物
定量蛋白质组学
蛋白质组
聚类分析
生物化学
压力(语言学)
蛋白质生物合成
战斗或逃跑反应
异质核核糖核蛋白
肽序列
模块化设计
P-体
RNA结合蛋白
作者
S.C. Fujita,Miyu Murata,Hyun‐Woo Rhee,Shin-Ichi Tate,Kyota Yasuda
标识
DOI:10.1016/j.biocel.2026.106961
摘要
Stress granules (SGs) are membraneless ribonucleoprotein condensates that form under stress and dissolve during recovery. While assembly mechanisms are well characterized, the temporal organization of disassembly remains incompletely understood. Here, we performed time-resolved proximity proteomics across SG disassembly (0-50 min recovery; n = 3) using G3BP1 as bait, identifying 79 proteins with robust temporal dynamics. Unsupervised clustering resolved five kinetic modules: early-increase, early-decrease/late-increase, transient-drop at ∼40 min, early-decrease, and zig-zag patterns. The transient-drop module was enriched for RNA-processing factors, consistent with transient changes in RNA-processing factor engagement. SYNCRIP, an hnRNP family protein in the early-decrease/late-increase module, showed characteristic biphasic dynamics during recovery. Functional validation demonstrated that SYNCRIP knockdown specifically impairs late-phase SG clearance-increasing granule size at 50 min recovery-without affecting formation. Together, our data provide a modular temporal map of SG disassembly and establish SYNCRIP as a functionally validated factor required for late-phase clearance.
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