Enhancing Sensitivity in Low-Load Proteomics Orbitrap Workflows via SLIM Integration

  • Liulin Deng*
  • , Brian Adamson
  • , Alan McKenzie-Coe
  • , Kyle L. Fort
  • , Tobias P. Wörner
  • , Oliver Bernhardt
  • , Roland Bruderer
  • , Tejas Gandhi
  • , Lukas Reiter
  • , Eloy R. Wouters
  • , Jean Jacques Dunyach
  • , Alexander Makarov
  • , Daniel DeBord
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

A Structures for Lossless Ion Manipulation-Orbitrap Exploris 480 (SLIM-OE) ion mobility mass spectrometry (IM-MS) platform was developed, integrating SLIM IM separation with Orbitrap MS analysis. A “staggered IMS” mode was designed to acquire IM-m/z two-dimensional heatmap data via direct infusion for method development, and an LC compatible SLIM-enabled data-independent acquisition (SLIM-DIA) workflow was implemented for low sample load proteomics analysis. The study evaluated IM separation across a broad m/z range of ions and demonstrated up to a 190× sensitivity enhancement in both IM-MS and IM-MS/MS modes of operation relative to operation in MS and MS/MS modes, respectively. The increased sensitivity improved protein coverage for the Qual/Quant QC Mix proteins. Compared to standard DIA, SLIM-DIA achieved a 2.3× increase in protein group identification from 2 ng of HeLa on the modified instrument, while maintaining quantitative capabilities. This research highlights the potential of the SLIM-OE IM-MS system to enhance proteomics analysis, providing a foundation for future high-performance SLIM-Orbitrap instrumentation development.

Original languageEnglish
Pages (from-to)12613-12622
Number of pages10
JournalAnalytical Chemistry
Volume97
Issue number24
DOIs
Publication statusPublished - 24 Jun 2025

Bibliographical note

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© 2025 American Chemical Society.

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