用于超高分辨率离子迁移率分析的迭代SLIM (itSLIM)。

IF 2.7 2区 化学 Q2 BIOCHEMICAL RESEARCH METHODS
Liulin Deng, Ding Zhang, Leonard C Rorrer, Michael J Slemko, Daniel DeBord
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引用次数: 0

摘要

我们提出了一种利用无损离子操作(SLIM)离子迁移-质谱(IM-MS)系统结构实现超高分辨率离子迁移(uhrm)分离的新方法。通过采用圆形离子路径设计,离子可以双向传输和分离,从而实现迭代工作流程,其中迁移分离的离子返回到蛇形路径的入口,同时保留其分离顺序和位置。这种“迭代SLIM”(itSLIM)过程可以重复多次,几乎没有目标离子损失,以增加迁移率分离的有效路径长度。由于IM分辨率与分离路径长度的平方根成正比,因此该方法在不增加移动器件外形因素的情况下提高了IM分辨率。在需要高特异性的地方,它特别有利于有针对性的流动性分析和自信的鉴定。在路径长度为120 m的条件下,以2.48的双峰分辨率实现了对18:1 Δ9-cis-和Δ9-trans-phosphatidylethanolamine (PE)脂质异构体的uhrm分离。通过将其在90 m路径上的slim分离与MS/MS碎片化分析相结合,实现了一种无液相色谱(LC)的工作流程,能够明确鉴定异构小分子药物去甲可待因和去甲氢可酮。uhrm分离简化了得到的MS/MS光谱,提高了鉴定精度。这样的功能有望通过减少或消除LC运行时间和筛选工作流的健壮性来提高吞吐量。迭代SLIM提供了增强IM分辨率的强大策略,为高性能分析分离提供了广泛的实用程序。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Iterative SLIM (itSLIM) for Ultrahigh Resolution Targeted Ion Mobility Analysis.

We present a novel approach for achieving ultrahigh-resolution ion mobility (UHRIM) separations using a structures for lossless ion manipulation (SLIM) ion mobility-mass spectrometry (IM-MS) system. By incorporating a rounded-turn ion path design, ions can be transmitted and separated bidirectionally, enabling an iterative workflow in which mobility-separated ions are returned to the entrance of the serpentine path while preserving their separation order and position. This "iterative SLIM" (itSLIM) process can be repeated multiple times with little to no target ion loss to increase the effective path length of the mobility separation. As IM resolution scales with the square root of the separation path length, this method enhances IM resolution without increasing the form factor of the mobility device. It is particularly beneficial for targeted mobility analysis and confident identification where high specificity is required. UHRIM separation was achieved with a two-peak resolution of 2.48 for 18:1 Δ9-cis- and Δ9-trans-phosphatidylethanolamine (PE) lipid isomers at a path length of 120 m. By combining itSLIM separation over a 90-m path with MS/MS fragmentation analysis, a liquid chromatography (LC)-free workflow capable of definitive identification of the isomeric small molecule drugs norcodeine and norhydrocodone was achieved. The UHRIM separation simplifies the resulting MS/MS spectra and improves identification accuracy. Such capabilities are anticipated to enhance the throughput by reducing or eliminating LC run times and robustness of screening workflows. Iterative SLIM provides a powerful strategy for enhancing IM resolution, offering broad utility for high-performance analytical separations.

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来源期刊
CiteScore
5.50
自引率
9.40%
发文量
257
审稿时长
1 months
期刊介绍: The Journal of the American Society for Mass Spectrometry presents research papers covering all aspects of mass spectrometry, incorporating coverage of fields of scientific inquiry in which mass spectrometry can play a role. Comprehensive in scope, the journal publishes papers on both fundamentals and applications of mass spectrometry. Fundamental subjects include instrumentation principles, design, and demonstration, structures and chemical properties of gas-phase ions, studies of thermodynamic properties, ion spectroscopy, chemical kinetics, mechanisms of ionization, theories of ion fragmentation, cluster ions, and potential energy surfaces. In addition to full papers, the journal offers Communications, Application Notes, and Accounts and Perspectives
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