Nanohydrophobic Interaction Chromatography Coupled to Ultraviolet Photodissociation Mass Spectrometry for the Analysis of Intact Proteins in Low Charge States

J Proteome Res. 2022 Oct 7;21(10):2493-2503. doi: 10.1021/acs.jproteome.2c00450. Epub 2022 Aug 31.

Abstract

The direct correlation between proteoforms and biological phenotype necessitates the exploration of mass spectrometry (MS)-based methods more suitable for proteoform detection and characterization. Here, we couple nano-hydrophobic interaction chromatography (nano-HIC) to ultraviolet photodissociation MS (UVPD-MS) for separation and characterization of intact proteins and proteoforms. High linearity, sensitivity, and sequence coverage are obtained with this method for a variety of proteins. Investigation of collisional cross sections of intact proteins during nano-HIC indicates semifolded conformations in low charge states, enabling a different dimension of separation in comparison to traditional, fully denaturing reversed-phase separations. This method is demonstrated for a mixture of intact proteins from Escherichia coli ribosomes; high sequence coverage is obtained for a variety of modified and unmodified proteoforms.

Keywords: collisional cross section (CCS); hydrophobic interaction chromatography (HIC); liquid chromatography (LC); mass spectrometry (MS); native mass spectrometry (nMS); orbitrap mass spectrometer; protein; proteoform; top-down mass spectrometry (TDMS); ultraviolet photodissociation (UVPD).

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Chromatography, Liquid / methods
  • Escherichia coli / genetics
  • Hydrophobic and Hydrophilic Interactions
  • Proteins*
  • Spectrophotometry, Ultraviolet / methods
  • Tandem Mass Spectrometry* / methods
  • Ultraviolet Rays

Substances

  • Proteins