描述动态线粒体-内质网接触部位的指南。

Antigoni Diokmetzidou, Luca Scorrano
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引用次数: 0

摘要

细胞器曾经被认为是独立的实体,但现在已经确定它们通过蛋白质系链和脂质相互作用维持的特殊膜接触来相互作用。其中,线粒体-内质网接触位点(MERCS)成为钙信号、脂质代谢和线粒体动力学的中枢。在这里,我们批判性地评估了MERC可视化和量化的当前方法,调查了分子工具箱的选择性扰动,并强调了常见的实验陷阱。我们还讨论了关键的概念问题——从结构和功能的角度定义merc,解决栓系因素之间的冗余,以及区分merc介导的原发性效应和继发性细胞反应。最后,我们建议将成像、精确生化分离、蛋白质组学和功能分析相结合的综合策略将是解决MERC生理和病理动力学方面悬而未决的问题所必需的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A guide to characterizing the dynamic mitochondria-endoplasmic reticulum contact sites.

Organelles were once regarded as discrete entities, but it is now established that they interact through specialized membrane contacts maintained by protein tethers and lipid interactions. Among these, mitochondria-endoplasmic reticulum contact sites (MERCS) emerged as hubs for calcium signaling, lipid metabolism, and mitochondrial dynamics. Here, we critically appraise current methodologies for MERC visualization and quantification, survey the molecular toolbox for their selective perturbation, and highlight common experimental pitfalls. We also discuss key conceptual issues-defining MERCs on structural and functional grounds, addressing redundancy among tethering factors, and distinguishing primary MERC-mediated effects from secondary cellular responses. Finally, we propose that an integrative strategy combining imaging, precise biochemical isolation, proteomics, and functional assays will be essential to resolve outstanding questions about MERC dynamics in physiology and pathology.

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