生物
ULK1
自噬
遗传学
计算生物学
细胞生物学
进化生物学
激酶
蛋白激酶A
细胞凋亡
安普克
作者
Devanarayanan Siva Sankar,Jörn Dengjel
出处
期刊:Autophagy
[Informa]
日期:2024-10-12
卷期号:: 1-3
标识
DOI:10.1080/15548627.2024.2414386
摘要
The ULK1 kinase complex plays a crucial role in autophagosome biogenesis. To identify interactors or regulators of ULK1 complex assembly influencing autophagosome biogenesis, we performed an interaction proteomics screen. Employing both affinity purification and proximity labeling of N- and C-terminal tagged fusion proteins coupled to quantitative mass spectrometry, we identified 317 high-confidence interactors or neighbors of the four ULK1 complex members, including both member-specific and common interactors. Interactions with selective macroautophagy/autophagy receptors indicate the activation of selective autophagy pathways by 90 min of nutrient starvation. Focusing on the ULK1 effector protein BAG2, a common interactor identified by both approaches, we highlight that ULK1 phosphorylates BAG2, supporting the localization of the scaffold and autophagy inducer AMBRA1 to the ER, thereby positively regulating autophagy initiation.
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