Online Nanoflow Reversed Phase-Strong Anion Exchange-Reversed Phase Liquid Chromatography-Tandem Mass Spectrometry Platform for Efficient and In-Depth Proteome Sequence Analysis of Complex Organisms

作者：Zhou Feng; Sikorski Timothy W; Ficarro Scott B; Webber James T; Marto Jarrod A^*

来源：Analytical Chemistry, 2011, 83(18): 6996-7005.

DOI：10.1021/ac200639v

The dynamic range of protein expression in complex organisms coupled with the stochastic nature of discovery-driven tandem mass spectrometry (MS/MS) analysis continues to impede comprehensive sequence analysis and often provides only limited information for low-abundance proteins. High-performance fractionation of proteins or peptides prior to mass spectrometry analysis can mitigate these effects, though achieving an optimal combination of automation, reproducibility, separation peak capacity, and sample yield remains a significant challenge. Here we demonstrate an automated nanoflow 3-D liquid chromatography (LC)-MS/MS platform based on high-pH reversed phase (RP), strong anion exchange (SAX), and low-pH reversed phase (RP) separation stages for analysis of complex proteomes. We observed that RP-SAX-RP outperformed RP-RP for analysis of tryptic peptides derived from Escherichia coli and enabled identification of proteins present at a level of SO copies per cell in Saccharomyces cerevisiae, corresponding to an estimated detection limit of 500 amol, from 40 mu g of total lysate on a low-resolution 3-D ion trap mass spectrometer. A similar study performed on a LTQ:Orbitrap yielded over 4000 unique proteins from 5 mu g of total yeast lysate analyzed in a single, 101 fraction RP-SAX-RP LC-MS/MS acquisition, providing an estimated detection limit of 65 amol for proteins expressed at 50 copies per cell.

• 出版日期2011-9-15