2
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Finding the Sweet Spot in ERLIC Mobile Phase for Simultaneous Enrichment of N-glyco and Phospho- Peptides

      research-article

      Read this article at

      ScienceOpenPublisherPMC
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Simultaneous enrichment of glyco- and phospho- peptides will benefit the studies of biological processes regulated by these post-translational modifications (PTMs). It will also reveal potential crosstalk between these two ubiquitous PTMs. Unlike custom designed multifunctional solid phase extraction (SPE) materials, operating strong-anion exchange (SAX) resin in electrostatic repulsion-hydrophilic interaction chromatography (ERLIC) mode provides a readily available strategy to analytical labs for enrichment of these PTMs for subsequent mass spectrometry (MS)-based characterization. However, the choice of mobile phase has largely relied on empirical rules from hydrophilic interaction chromatography (HILIC) or ion-exchange chromatography (IEX) without further optimization and adjustments. In this study, ten mobile phase compositions of ERLIC were systematically compared; the impact of multiple factors including organic phase proportion, ion pairing reagent, pH and salt on the retention of glycosylated and phosphorylated peptides were evaluated. This study demonstrated good enrichment of glyco- and phospho- peptides from the nonmodified peptides in a complex tryptic digest. Moreover, the enriched glyco- and phospho- peptides elute in different fractions by orthogonal retention mechanisms of hydrophilic interaction and electrostatic interaction in ERLIC, maximizing the LC-MS identification of each PTM. The optimized mobile phase can be adapted to the ERLIC HPLC system, where the high resolution in separating multiple PTMs will benefit large-scale MS-based PTM profiling and in-depth characterization.

          Graphical Abstract

          Related collections

          Author and article information

          Journal
          9010412
          21031
          J Am Soc Mass Spectrom
          J. Am. Soc. Mass Spectrom.
          Journal of the American Society for Mass Spectrometry
          1044-0305
          1879-1123
          22 July 2019
          08 July 2019
          December 2019
          01 December 2020
          : 30
          : 12
          : 2491-2501
          Affiliations
          [1 ]Department of Chemistry, University of Wisconsin, Madison, WI 53706, USA
          [2 ]School of Pharmacy, University of Wisconsin, Madison, WI 53705, USA
          Author notes
          [* ]Address reprint requests to: Dr. Lingjun Li, School of Pharmacy & Department of Chemistry, University of Wisconsin, 777 Highland Ave, Madison, WI 53705., lingjun.li@ 123456wisc.edu . Phone: (608)265-8491, Fax: (608)262-5345.
          Article
          PMC6917886 PMC6917886 6917886 nihpa1533894
          10.1007/s13361-019-02230-6
          6917886
          31286442
          9504da3c-f9b3-445b-b522-5feda8228f13

          Terms of use and reuse: academic research for non-commercial purposes, see here for full terms. http://www.springer.com/gb/open-access/authors-rights/aam-terms-v1

          History
          Categories
          Article

          Comments

          Comment on this article