一种基于 APEX2 的具有时间特异性的近距离依赖性生物素化测定法,用于研究酿酒酵母自噬过程中的蛋白质相互作用。

Autophagy Pub Date : 2024-10-01 Epub Date: 2024-07-03 DOI:10.1080/15548627.2024.2366749
Yasmina Filali-Mouncef, Alexandre Leytens, Prado Vargas Duarte, Mattia Zampieri, Jörn Dengjel, Fulvio Reggiori
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引用次数: 0

摘要

自噬体的生物生成是一个复杂的过程,由 Atg(自噬相关)蛋白之间的动态相互作用协调,并以特定货物的周转为特征。蛋白质组分析是揭示蛋白质-蛋白质相互作用网络的核心,当与依赖于近距离的生物素化或近距离标记(PL)方法相结合时,它们还能检测瞬时和微弱的相互作用。然而,作为研究自噬的主要模型之一,目前用于酵母菌的近距离标记程序无法保持时间特异性,因此无法在自噬诱导后的精确时间点识别相互作用和货物。在这里,我们提出了一种新的基于抗坏血酸过氧化物酶 2(APEX2)的 PL 方案,它适用于酵母,能保持时间特异性,并能通过 Western 印迹或蛋白质组学发现邻近蛋白。作为概念验证,我们应用这种新方法鉴定了Atg8和Atg9的相互作用者,并在富氮和氮饥饿条件下检测到了已知的结合伙伴以及潜在的未表征伙伴。此外,作为概念验证,我们还证实了 Atg8 和 Faa1 之间的空间接近相互作用。我们相信,对于所有研究酵母自噬机制和作用的研究人员来说,这一方案将是一个新的重要实验工具,同时也是研究这一模式生物中其他细胞通路的重要工具:缩写:APEX2,抗坏血酸过氧化物酶 2;Atg,自噬相关;BP,生物素苯酚;Cvt,细胞质到液泡靶向;ER,内质网;LN2,液氮;MS,质谱;PAS,吞噬细胞组装位点;PL,接近标记;PE,磷脂酰乙醇胺;PPINs,蛋白质-蛋白质相互作用网络;PPIs,蛋白质-蛋白质相互作用;RT,室温;SARs,选择性自噬受体;WT,野生型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An APEX2-based proximity-dependent biotinylation assay with temporal specificity to study protein interactions during autophagy in the yeast Saccharomyces cerevisiae.

Autophagosome biogenesis is a complex process orchestrated by dynamic interactions between Atg (autophagy-related) proteins and characterized by the turnover of specific cargoes, which can differ over time and depending on how autophagy is stimulated. Proteomic analyses are central to uncover protein-protein interaction networks and when combined with proximity-dependent biotinylation or proximity labeling (PL) approaches, they also permit to detect transient and weak interactions. However, current PL procedures for yeast Saccharomyces cerevisiae, one of the leading models for the study of autophagy, do not allow to keep temporal specificity and thus identify interactions and cargoes at a precise time point upon autophagy induction. Here, we present a new ascorbate peroxidase 2 (APEX2)-based PL protocol adapted to yeast that preserves temporal specificity and allows uncovering neighbor proteins by either western blot or proteomics. As a proof of concept, we applied this new method to identify Atg8 and Atg9 interactors and detected known binding partners as well as potential uncharacterized ones in rich and nitrogen starvation conditions. Also, as a proof of concept, we confirmed the spatial proximity interaction between Atg8 and Faa1. We believe that this protocol will be a new important experimental tool for all those researchers studying the mechanism and roles of autophagy in yeast, but also other cellular pathways in this model organism.Abbreviations: APEX2, ascorbate peroxidase 2, Atg, autophagy-related; BP, biotin phenol; Cvt, cytoplasm-to-vacuole targeting; ER, endoplasmic reticulum; LN2, liquid nitrogen; MS, mass spectrometry; PAS, phagophore assembly site; PL, proximity labeling; PE, phosphatidylethanolamine; PPINs, protein-protein interaction networks; PPIs, protein-protein interactions; RT, room temperature; SARs, selective autophagy receptors; WT, wild-type.

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