Capillary electrophoresis-mass spectrometry for protein analyses under native conditions: Current progress and perspectives

Ann Katrin Schwenzer, Lena Kruse, Kevin Jooß*, Christian Neusüß

*Corresponding author for this work

Research output: Contribution to JournalReview articleAcademicpeer-review

Abstract

Native mass spectrometry is a rapidly emerging technique for fast and sensitive structural analysis of protein constructs, maintaining the protein higher order structure. The coupling with electromigration separation techniques under native conditions enables the characterization of proteoforms and highly complex protein mixtures. In this review, we present an overview of current native CE-MS technology. First, the status of native separation conditions is described for capillary zone electrophoresis (CZE), affinity capillary electrophoresis (ACE), and capillary isoelectric focusing (CIEF), as well as their chip-based formats, including essential parameters such as electrolyte composition and capillary coatings. Further, conditions required for native ESI-MS of (large) protein constructs, including instrumental parameters of QTOF and Orbitrap systems, as well as requirements for native CE-MS interfacing are presented. On this basis, methods and applications of the different modes of native CE-MS are summarized and discussed in the context of biological, medical, and biopharmaceutical questions. Finally, key achievements are highlighted and concluded, while remaining challenges are pointed out.

Original languageEnglish
Article number2300135
Number of pages22
JournalProteomics
Volume24
Issue number3-4
Early online date13 Jun 2023
DOIs
Publication statusPublished - Feb 2024

Bibliographical note

Funding Information:
This study was funded by the German Federal Ministery for Education and Research within the ProCEVen project (FKZ 13FH135KX0).

Publisher Copyright:
© 2023 The Authors. Proteomics published by Wiley-VCH GmbH.

Funding

This study was funded by the German Federal Ministery for Education and Research within the ProCEVen project (FKZ 13FH135KX0).

Keywords

  • biopharmaceutical proteins
  • higher order structure
  • microfluidics
  • native capillary electrophoresis-mass spectrometry
  • protein complexes and conformations

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