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快速亲水作用色谱-离子淌度质谱联用(RHIMMS)方法用于复杂生物样品的非靶向代谢组学分析。

Rapid HILIC-Z ion mobility mass spectrometry (RHIMMS) method for untargeted metabolomics of complex biological samples.

机构信息

Institute of Quantitative Biology, Biochemistry and Biotechnology, University of Edinburgh, Max Born Crescent, Edinburgh, EH9 3BF, UK.

EdinOmics, University of Edinburgh, Max Born Crescent, Edinburgh, EH9 3BF, UK.

出版信息

Metabolomics. 2022 Feb 28;18(3):16. doi: 10.1007/s11306-022-01871-1.

Abstract

INTRODUCTION

Recent advances in high-throughput methodologies in the 'omics' and synthetic biology fields call for rapid and sensitive workflows in the metabolic phenotyping of complex biological samples.

OBJECTIVE

The objective of this research was to evaluate a straightforward to implement LC-MS metabolomics method using a commercially available chromatography column that provides increased throughput. Reducing run time can potentially impact chromatography and therefore the effects of ion mobility spectrometry to expand peak capacity were also evaluated. Additional confidence provided via collision cross section measurements for detected features was also explored.

METHODS

A rapid untargeted metabolomics workflow was developed with broad metabolome coverage, combining zwitterionic-phase hydrophilic interaction chromatography (HILIC-Z) with drift tube ion mobility-quadrupole time-of-flight (DTIM-qTOF) mass spectrometry. The analytical performance of our method was explored using extracts from complex biological samples, including a reproducibility study on chicken serum and a simple comparative study on a bacterial metabolome.

RESULTS

The method is acronymised RHIMMS for rapid HILIC-Z ion mobility mass spectrometry. We present the RHIMMS workflow starting with data acquisition, followed by data processing and analysis. RHIMMS demonstrates improved chromatographic separation for a selection of metabolites with wide physicochemical properties while maintaining reproducibility at better than 20% over 200 injections at 3.5 min per sample for the selected metabolites, and a mean of 13.9% for the top 50 metabolites by intensity. Additionally, the combination of rapid chromatographic separation with ion mobility allows improved annotation and the ability to distinguish isobaric compounds.

CONCLUSION

Our results demonstrate RHIMMS to be a rapid, reproducible, sensitive and high-resolution analytical platform that is highly applicable to the untargeted metabolomics analysis of complex samples.

摘要

简介

高通量方法在“组学”和合成生物学领域的最新进展要求对复杂生物样本的代谢表型进行快速、灵敏的工作流程。

目的

本研究的目的是评估一种使用商业可得的色谱柱实现的简单可实施的 LC-MS 代谢组学方法,该色谱柱可提高通量。缩短运行时间可能会影响色谱,因此还评估了离子淌度谱扩展峰容量的效果。还探索了通过检测到的特征的碰撞截面测量值提供额外的置信度。

方法

开发了一种快速的非靶向代谢组学工作流程,具有广泛的代谢组覆盖范围,结合两性离子亲水作用色谱(HILIC-Z)与漂移管离子淌度-四极杆飞行时间(DTIM-qTOF)质谱联用。使用复杂生物样本的提取物探索了我们方法的分析性能,包括鸡血清的重现性研究和细菌代谢组的简单比较研究。

结果

该方法的缩写为 RHIMMS,代表快速 HILIC-Z 离子淌度质谱。我们提出了 RHIMMS 工作流程,从数据采集开始,然后是数据处理和分析。RHIMMS 展示了对具有广泛物理化学性质的选定代谢物的色谱分离的改进,同时在 3.5 分钟内每样品 200 次注射时保持超过 20%的重现性,所选代谢物的平均重现性为 13.9%,按强度计算为前 50 种代谢物的平均重现性。此外,快速色谱分离与离子淌度的结合允许改进注释并能够区分等摩尔化合物。

结论

我们的结果表明 RHIMMS 是一种快速、可重复、灵敏且高分辨率的分析平台,非常适用于复杂样品的非靶向代谢组学分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ad1/8885480/e869c2e645d1/11306_2022_1871_Fig1_HTML.jpg

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