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使用循环离子淌度谱仪进行串联离子淌度实验。

Using a Cyclic Ion Mobility Spectrometer for Tandem Ion Mobility Experiments.

机构信息

INRAE, UR BIA, F-44316 Nantes, France; INRAE, BIBS Facility, F-44316 Nantes, France.

INRAE, UR BIA, F-44316 Nantes, France; INRAE, BIBS Facility, F-44316 Nantes, France;

出版信息

J Vis Exp. 2022 Jan 20(179). doi: 10.3791/63451.

Abstract

Accurate characterization of chemical structures is important to understand their underlying biological mechanisms and functional properties. Mass spectrometry (MS) is a popular tool but is not always sufficient to completely unveil all structural features. For example, although carbohydrates are biologically relevant, their characterization is complicated by numerous levels of isomerism. Ion mobility spectrometry (IMS) is an interesting complement because it is sensitive to ion conformations and, thus, to isomerism. Furthermore, recent advances have significantly improved the technique: the last generation of Cyclic IMS instruments offers additional capabilities compared to linear IMS instruments, such as an increased resolving power or the possibility to perform tandem ion mobility (IMS/IMS) experiments. During IMS/IMS, an ion is selected based on its ion mobility, fragmented, and reanalyzed to obtain ion mobility information about its fragments. Recent work showed that the mobility profiles of the fragments contained in such IMS/IMS data can act as a fingerprint of a particular glycan and can be used in a molecular networking strategy to organize glycomics datasets in a structurally relevant way. The goal of this protocol is thus to describe how to generate IMS/IMS data, from sample preparation to the final Collision Cross Section (CCS) calibration of the ion mobility dimension that yields reproducible spectra. Taking the example of one representative glycan, this protocol will show how to build an IMS/IMS control sequence on a Cyclic IMS instrument, how to account for this control sequence to translate IMS arrival time into drift time (i.e., the effective separation time applied to the ions), and how to extract the relevant mobility information from the raw data. This protocol is designed to clearly explain the critical points of an IMS/IMS experiment and thus help new Cyclic IMS users perform straightforward and reproducible acquisitions.

摘要

准确地表征化学结构对于理解其潜在的生物学机制和功能特性非常重要。质谱(MS)是一种常用的工具,但并不总是足以完全揭示所有的结构特征。例如,尽管碳水化合物具有生物学相关性,但由于其异构现象的存在,其特征描述变得复杂。离子淌度谱(IMS)是一种很有意义的补充方法,因为它对离子构象敏感,因此对异构现象敏感。此外,最近的进展显著提高了该技术:与线性 IMS 仪器相比,最新一代的循环 IMS 仪器具有附加功能,例如提高分辨率或进行串联离子淌度(IMS/IMS)实验的可能性。在 IMS/IMS 中,根据离子的淌度选择离子,使其碎片化,并重新分析以获得其碎片的离子淌度信息。最近的工作表明,这种 IMS/IMS 数据中的碎片的淌度谱可以作为特定聚糖的指纹,并可以用于分子网络策略,以结构相关的方式组织糖组学数据集。本方案的目标是描述如何从样品制备到离子淌度维度的最终碰撞截面(CCS)校准生成 IMS/IMS 数据,以产生可重复的光谱。以一种代表性聚糖为例,本方案将展示如何在循环 IMS 仪器上构建 IMS/IMS 控制序列,如何考虑该控制序列将 IMS 到达时间转换为漂移时间(即,应用于离子的有效分离时间),以及如何从原始数据中提取相关的淌度信息。本方案旨在清楚地解释 IMS/IMS 实验的关键点,从而帮助新的循环 IMS 用户进行简单且可重复的采集。

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