Abstract

Data-independent acquisition mass spectrometry (DIA-MS) is essential for information-rich spectral annotations in untargeted metabolomics. However, the acquired MS2 spectra are highly complex, posing significant annotation challenges. We have developed a correlation-based deconvolution (CorrDec) method that uses ion abundance correlations in multisample studies using DIA-MS as an update of our MS-DIAL software. CorrDec is based on the assumption that peak intensities of precursor and fragment ions correlate across samples and exploits this quantitative information to deconvolute complex DIA spectra. CorrDec clearly improved deconvolution of the original MS-DIAL deconvolution method (MS2Dec) in a dilution series of chemical standards and a 224-sample urinary metabolomics study. The primary advantage of CorrDec over MS2Dec is the ability to discriminate coeluting low-abundance compounds. CorrDec requires the measurement of multiple samples to successfully deconvolute DIA spectra; however, our randomized assessment demonstrated that CorrDec can contribute to studies with as few as 10 unique samples. The presented methodology improves compound annotation and identification in multisample studies and will be useful for applications in large cohort studies.

Highlights

  • Data-independent acquisition mass spectrometry (DIA-MS) is essential for information-rich spectral annotations in untargeted metabolomics

  • We present a new MS2 deconvolution method based on the correlation of ion abundances between precursor and product ions among biological samples, named correlation-based deconvolution (CorrDec) (Correlationbased Deconvolution)

  • Article is based on three assumptions: (1) metabolite concentrations differ across study samples in multisample studies; (2) the MS2 fragmentation pattern is identical under identical experimental conditions; (3) intensities of fragment ions correlate with those of their precursors

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Summary

Introduction

Data-independent acquisition mass spectrometry (DIA-MS) is essential for information-rich spectral annotations in untargeted metabolomics. Step 2: All correlation values in all features are integrated into a matrix based on the m/z of the product ion using the same m/z threshold (0.01 in this study) as MS2Mat (Figure 1B).

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