优化蛋白质组还原整合自顶向下蛋白质组学。

IF 4 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Proteomes Pub Date : 2023-03-06 DOI:10.3390/proteomes11010010
Breyer Woodland, Aleksandar Necakov, Jens R Coorssen
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引用次数: 3

摘要

综合自顶向下的蛋白质组学是一种分析方法,充分解决了有效和常规评估蛋白质组所需的广度和复杂性。然而,任何这样的评估也需要对方法进行严格的审查,以确保最深入的定量蛋白质组分析。在这里,我们建立了一个优化的蛋白质组提取的通用方案,以提高蛋白质形态的还原,从而提高2DE的分辨率。二硫苏糖醇(DTT)、三丁基膦(TBP)和2-羟乙基二硫醚(HED),联合和单独,在一维SDS-PAGE (1DE)中进行测试,然后进入完整的2DE协议。在样品再水化之前,与文献中报道的其他条件和还原方案相比,用100 mM DTT + 5 mM TBP还原可以增加斑点计数、总信号和斑点圆度(即减少条纹)。数据表明,许多广泛实施的还原协议在蛋白质形态还原方面明显“动力不足”,从而限制了常规自上而下的蛋白质组学分析的质量和深度。
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Optimized Proteome Reduction for Integrative Top-Down Proteomics.

Integrative top-down proteomics is an analytical approach that fully addresses the breadth and complexity needed for effective and routine assessment of proteomes. Nonetheless, any such assessments also require a rigorous review of methodology to ensure the deepest possible quantitative proteome analyses. Here, we establish an optimized general protocol for proteome extracts to improve the reduction of proteoforms and, thus, resolution in 2DE. Dithiothreitol (DTT), tributylphosphine (TBP), and 2-hydroxyethyldisulfide (HED), combined and alone, were tested in one-dimensional SDS-PAGE (1DE), prior to implementation into a full 2DE protocol. Prior to sample rehydration, reduction with 100 mM DTT + 5 mM TBP yielded increased spot counts, total signal, and spot circularity (i.e., decreased streaking) compared to other conditions and reduction protocols reported in the literature. The data indicate that many widely implemented reduction protocols are significantly 'under-powered' in terms of proteoform reduction and thus, limit the quality and depth of routine top-down proteomic analyses.

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来源期刊
Proteomes
Proteomes Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
6.50
自引率
3.00%
发文量
37
审稿时长
11 weeks
期刊介绍: Proteomes (ISSN 2227-7382) is an open access, peer reviewed journal on all aspects of proteome science. Proteomes covers the multi-disciplinary topics of structural and functional biology, protein chemistry, cell biology, methodology used for protein analysis, including mass spectrometry, protein arrays, bioinformatics, HTS assays, etc. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of papers. Scope: -whole proteome analysis of any organism -disease/pharmaceutical studies -comparative proteomics -protein-ligand/protein interactions -structure/functional proteomics -gene expression -methodology -bioinformatics -applications of proteomics
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