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Analyst. 2015 Feb 21;140(4):1314-22. doi: 10.1039/c4an02119c.

Systematic comparison between SDS-PAGE/RPLC and high-/low-pH RPLC coupled tandem mass spectrometry strategies in a whole proteome analysis.

Author information

1
Department of Chemistry and Institutes of Biomedical Science Shanghai Medical School, Fudan University, Shanghai 200032, China. shenhuali@fudan.edu.cn pyyang@fudan.edu.cn.

Abstract

SDS-PAGE and high-pH RPLC are commonly used fractionation strategies in proteomics research. A comparative investigation of these two strategies would be meaningful to thoroughly understand their respective features. Here, we systematically compared the two methods by trying 4 SDS-PAGE/RPLC and 3 high-/low-pH RPLC different workflows for a higher sensitivity in protein identification. Totally 9793 proteins were identified in HepG2 cells, with 8581 proteins identified by high-/low-pH RPLC workflows and 7933 by SDS-PAGE/RPLC workflows. The results demonstrate that using high-pH RPLC in the first dimensional separation would favour a high-throughput proteome analysis but choosing SDS-PAGE could yield much better peptide coverage. We found that the SDS-PAGE fractionation method benefits the neutral pI peptides. We also analyzed unexpected modifications caused by the two strategies. Our results suggest that more pre-fractionation benefits protein identifications in both strategies and pooling of gel pieces according to their grey values increased the identification efficiency in SDS-PAGE/RPLC workflows.

PMID:
25574523
DOI:
10.1039/c4an02119c
[Indexed for MEDLINE]

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