化学
轨道轨道
工作流程
灵敏度(控制系统)
蛋白质组学
色谱法
质谱法
数据库
生物化学
计算机科学
电子工程
基因
工程类
作者
Liulin Deng,Brian Adamson,Alan McKenzie‐Coe,Kyle L. Fort,Tobias P. Wörner,Oliver M. Bernhardt,Roland Bruderer,Tejas Gandhi,Lukas Reiter,Eloy R. Wouters,Jean‐Jacques Dunyach,Alexander Makarov,Daniel DeBord
标识
DOI:10.1021/acs.analchem.5c00897
摘要
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.
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