Correlation-Based Deconvolution (CorrDec) To Generate High-Quality MS2 Spectra from Data-Independent Acquisition in Multisample Studies.
Ipputa TadaRomanas ChaleckisHiroshi TsugawaIsabel MeisterPei ZhangNikolaos LazarinisBarbro DahlénCraig E WheelockMasanori AritaPublished in: Analytical chemistry (2020)
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.
Keyphrases
- mass spectrometry
- liquid chromatography
- multiple sclerosis
- gas chromatography
- ms ms
- high performance liquid chromatography
- capillary electrophoresis
- high resolution
- density functional theory
- high resolution mass spectrometry
- magnetic resonance imaging
- clinical trial
- case control
- magnetic resonance
- tandem mass spectrometry
- optical coherence tomography
- electronic health record
- rna seq
- social media
- double blind
- health information
- antibiotic resistance genes
- single cell
- artificial intelligence