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VDACs Post-Translational Modifications Discovery by Mass Spectrometry: Impact on Their Hub Function

期刊

出版社

MDPI
DOI: 10.3390/ijms222312833

关键词

voltage dependent anion channel; cysteine overoxidation; deamidation; hydroxyapatite; high-resolution mass spectrometry; post-translational modifications

资金

  1. Piano della Ricerca di Ateneo PIACERI 2020 of the University of Catania, Italy
  2. MIUR PNR Proof of Concept 2018 grant [PEPSLA POC 01_00054]

向作者/读者索取更多资源

VDAC (voltage-dependent anion selective channel) proteins, also known as mitochondrial porins, are crucial in cellular processes, metabolism regulation, and survival pathways due to their abundance and function as cellular hubs. Their structural characterization poses challenges due to high hydrophobicity, low solubility, and difficulty in isolation, leading to a need for analysis as components of a complex mixture. Recent advancements in tools such as nano-reversed phase ultra-high performance liquid chromatography (nanoRP-UHPLC) and ultra-sensitive high-resolution mass spectrometry (HRMS) have greatly contributed to the understanding of post-translational modifications (PTMs) of VDAC proteins.
VDAC (voltage-dependent anion selective channel) proteins, also known as mitochondrial porins, are the most abundant proteins of the outer mitochondrial membrane (OMM), where they play a vital role in various cellular processes, in the regulation of metabolism, and in survival pathways. There is increasing consensus about their function as a cellular hub, connecting bioenergetics functions to the rest of the cell. The structural characterization of VDACs presents challenging issues due to their very high hydrophobicity, low solubility, the difficulty to separate them from other mitochondrial proteins of similar hydrophobicity and the practical impossibility to isolate each single isoform. Consequently, it is necessary to analyze them as components of a relatively complex mixture. Due to the experimental difficulties in their structural characterization, post-translational modifications (PTMs) of VDAC proteins represent a little explored field. Only in recent years, the increasing number of tools aimed at identifying and quantifying PTMs has allowed to increase our knowledge in this field and in the mechanisms that regulate functions and interactions of mitochondrial porins. In particular, the development of nano-reversed phase ultra-high performance liquid chromatography (nanoRP-UHPLC) and ultra-sensitive high-resolution mass spectrometry (HRMS) methods has played a key role in this field. The findings obtained on VDAC PTMs using such methodologies, which permitted an in-depth characterization of these very hydrophobic trans-membrane pore proteins, are summarized in this review.

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