BAG3 蛋白相互作用在心肌病中的作用

Huiqi Qu, JuFang Wang, Alexandre Rosa Campos, Hakon Hakonarson, Arthur Feldman
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摘要

背景:Bcl-2-associated athanogene 3(BAG3)在细胞蛋白质质量控制(PQC)中发挥着维持蛋白质组稳定性的重要功能。BAG3 基因突变会导致心肌病。由于 BAG3 在心肌病中的作用以及 BAG3 蛋白相互作用的复杂性,鉴于多功能伴侣 BAG3 在心肌细胞中的重要性,利用体外心肌细胞模型了解这些蛋白相互作用非常重要:方法:使用高压液相色谱耦合串联质谱(LC-MS/MS)技术和 BioID 技术在人 AC16 心肌细胞系中进行实验检测:结果:在特发性心肌病和/或缺血性疾病中富集的所有 28 个标志基因组中都发现了与 BAG3 相互作用的蛋白质。在同时富集于特发性心肌病和缺血性疾病的 24 个标志基因集中,15 个基因集中至少有 3 个蛋白质与 BAG3 相互作用:本研究强调了 BAG3 蛋白的相互作用,揭示了心肌病中受影响的关键基因组,有助于解释 BAG3 保护心脏作用的分子机制。此外,本研究还强调了与 BAG3 相互作用的蛋白质的复杂性,这意味着 BAG3 会产生不必要的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of BAG3 protein interactions in cardiomyopathies
Background: Bcl-2-associated athanogene 3 (BAG3) plays an important function in cellular protein quality control (PQC) maintaining proteome stability. Mutations in the BAG3 gene result in cardiomyopathies. Due to its roles in cardiomyopathies and the complexity of BAG3-protein interactions, it is important to understand these protein interactions given the importance of the multifunctional cochaperone BAG3 in cardiomyocytes, using an in vitro cardiomyocyte model. Methods: The experimental assay was done using high pressure liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS) in the human AC16 cardiomyocyte cell line with the BioID technology. Results: Proteins with BAG3-interaction were identified in all the 28 hallmark gene sets enriched in idiopathic cardiomyopathies and/or ischemic disease. Among the 24 hallmark gene sets enriched in both idiopathic cardiomyopathies and ischemic disease, 15 gene sets had at least 3 proteins with BAG3-interaction. Conclusions: This study highlights BAG3 protein interactions, unveiling the key gene sets affected in cardiomyopathies, which help to explain the molecular mechanisms of the cardioprotective effects of BAG3. In addition, this study also highlighted the complexity of proteins with BAG3 interactions, implying unwanted effects of BAG3.
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