Implementation of a multiple‐fraction concatenation strategy in an online two‐dimensional high‐/low‐pH reversed‐phase/reversed‐phase liquid chromatography platform for qualitative and quantitative shotgun proteomic analyses. (7th July 2020)

• Record Type: Journal Article
• Authors: Law, Henry C.H.; Kong, Ricky P.W.; Li, Mengzhu; Szeto, Samuel S.W.; Chu, Ivan K.
• Other Names: Chu Ivan K. guestEditor.; O'Hair Richard A. J. guestEditor.; Siu K. W. Michael guestEditor.; Jiang Guibin guestEditor.; Wada Yoshinao guestEditor.; Siu‐Kwan Sze Newman guestEditor.; Oh Han Bin guestEditor.; Shiea Jentaie guestEditor.; Armentrout Peter B. guestEditor.
• Is Part Of: Journal of mass spectrometry. Volume 56:Number 4(2021)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2020-07-07
• Subjects: Mass spectrometry -- Periodicals; 543.65
• DOI: 10.1002/jms.4591
• Languages: English
• ISSNs: 1076-5174

Abstract

Abstract: Multidimensional liquid chromatography is the mainstay separation technique used for shotgun proteomic analyses. The application of a multiple‐fraction concatenation (MFC) strategy can result in a more disperse and consistent peptide elution profile across different fractions, when compared with a conventional strategy. Herein, we present the first automated online RP‐RP platform implementing an MFC strategy to facilitate robust, unattended, routine proteomic analyses. The improved duty cycle utilization of the MFC strategy led to an increase of 9% in the separation space occupancy and increases of approximately 10% in the identification of both proteins and peptides. The peptides uniquely identified by the MFC strategy were significantly biased toward those of acidic nature, with increased precursor signals leading to improved MS/MS spectral quality and enhanced acidic peptide identification. These improvements in qualitative analysis using the MFC strategy were also extended to quantitative analysis. When the acquired proteome was quantified with a normalized spectral abundance factor, the additionally acquired acidic peptides were a critical factor leading to enhanced reproducibility of quantitation using the MFC strategy. With merits of superior qualitative and quantitative characteristics over the conventional strategy, the MFC strategy appears to be a highly amenable technique for enhancing the separation capacity for routine proteomic analyses.