Heart-cut nano-LC-CZE-MS for the characterization of proteins on the intact level

Electrophoresis. 2019 Apr;40(7):1061-1065. doi: 10.1002/elps.201800411. Epub 2019 Jan 4.

Abstract

Multidimensional separation techniques play an increasingly important role in separation science, especially for the analysis of complex samples such as proteins. The combination of reversed-phase liquid chromatography in the nanoscale and CZE is especially beneficial due to their nearly orthogonal separation mechanism and well-suited geometries/dimensions. Here, a heart-cut nano-LC-CZE-MS setup was developed utilizing for the first time a mechanical 4-port valve as LC-CE interface. A model protein mixture containing four different protein species was first separated by nano LC followed by a heart-cut transfer of individual LC peaks and subsequent CZE-MS analysis. In the CZE dimension, various glycoforms of one protein species were separated. Improved separation capabilities were achieved compared to the 1D methods, which was exemplarily shown for ribonuclease B and its different glycosylated forms. LODs in the lower μg/mL range were determined, which are considerably lower compared to traditional CZE-MS. In addition, this study represents the first application of an LC-CE-MS system for intact protein analysis. The nano-LC-CZE-MS system is expected to be applicable to various other analytical challenges.

Keywords: Glycoproteins; LC-CE interfacing; Mechanical valve; Two-dimensional separation.

MeSH terms

  • Chromatography, Reverse-Phase / instrumentation
  • Chromatography, Reverse-Phase / methods
  • Electrophoresis, Capillary / instrumentation
  • Electrophoresis, Capillary / methods
  • Glycosylation
  • Hydrogen-Ion Concentration
  • Limit of Detection
  • Ribonucleases / analysis*
  • Tandem Mass Spectrometry / instrumentation
  • Tandem Mass Spectrometry / methods

Substances

  • Ribonucleases
  • ribonuclease B