Evaluation of Strong Cation Exchange versus Isoelectric Focusing of Peptides for Multidimensional Liquid Chromatography-Tandem Mass Spectrometry

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• 作者：Robbert J. C. Slebos ; Jonathan W. C. Brock ; Nancy F. Winters ; Sarah R. Stuart ; Misti A. Martinez ; Ming Li ; Mathew C. Chambers ; Lisa J. Zimmerman ; Amy J. Ham ; David L. Tabb ; Daniel C. Liebler
• 刊名：Journal of Proteome Research
• 出版年：2008
• 出版时间：December 5, 2008
• 年：2008
• 卷：7
• 期：12
• 页码：5286-5294
• 全文大小：332K
• 年卷期：v.7,no.12(December 5, 2008)
• ISSN：1535-3907

文摘

Shotgun proteome analysis platforms based on multidimensional liquid chromatography-tandem mass spectrometry (LC-MS/MS) provide a powerful means to discover biomarker candidates in tissue specimens. Analysis platforms must balance sensitivity for peptide detection, reproducibility of detected peptide inventories and analytical throughput for protein amounts commonly present in tissue biospecimens (<100 μg), such that platform stability is sufficient to detect modest changes in complex proteomes. We compared shotgun proteomics platforms by analyzing tryptic digests of whole cell and tissue proteomes using strong cation exchange (SCX) and isoelectric focusing (IEF) separations of peptides prior to LC-MS/MS analysis on a LTQ-Orbitrap hybrid instrument. IEF separations provided superior reproducibility and resolution for peptide fractionation from samples corresponding to both large (100 μg) and small (10 μg) protein inputs. SCX generated more peptide and protein identifications than did IEF with small (10 μg) samples, whereas the two platforms yielded similar numbers of identifications with large (100 μg) samples. In nine replicate analyses of tryptic peptides from 50 μg colon adenocarcinoma protein, overlap in protein detection by the two platforms was 77% of all proteins detected by both methods combined. IEF more quickly approached maximal detection, with 90% of IEF-detectable medium abundance proteins (those detected with a total of 3−4 peptides) detected within three replicate analyses. In contrast, the SCX platform required six replicates to detect 90% of SCX-detectable medium abundance proteins. High reproducibility and efficient resolution of IEF peptide separations make the IEF platform superior to the SCX platform for biomarker discovery via shotgun proteomic analyses of tissue specimens.