蛋白质组
分馏
色谱法
蛋白质组学
洗脱
样品制备
赫拉
化学
生物化学
细胞
基因
作者
Miljan Kuljanin,Dylan Z. Dieters‐Castator,David A. Hess,Lynne‐Marie Postovit,Gilles Lajoie
出处
期刊:Proteomics
[Wiley]
日期:2017-01-01
卷期号:17 (1-2)
被引量:37
标识
DOI:10.1002/pmic.201600337
摘要
Numerous workflows exist for large‐scale bottom‐up proteomics, many of which achieve exceptional proteome depth. Herein, we evaluated the performance of several commonly used sample preparation techniques for proteomic characterization of HeLa lysates [unfractionated in‐solution digests, SDS‐PAGE coupled with in‐gel digestion, gel‐eluted liquid fraction entrapment electrophoresis (GELFrEE) technology, SCX StageTips and high‐/low‐pH reversed phase fractionation (HpH)]. HpH fractionation was found to be superior in terms of proteome depth (>8400 proteins detected) and fractionation efficiency compared to other techniques. SCX StageTip fractionation required minimal sample handling and was also a substantial improvement over SDS‐PAGE separation and GELFrEE technology. Sequence coverage of the HeLa proteome increased to 38% when combining all workflows, however, total proteins detected improved only slightly to 8710. In summary, HpH fractionation and SCX StageTips are robust techniques and highly suited for complex proteome analysis.
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