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Cumulative Neutral Loss Model for Fragment Deconvolution in Electrospray Ionization High-Resolution Mass Spectrometry Data

Authors :
Denice van Herwerden
Jake O'Brien
Sascha Lege
Bob Pirok
Kevin Thomas
Saer Samanipour
Publication Year :
2023
Publisher :
American Chemical Society (ACS), 2023.

Abstract

Fragment deconvolution is a crucial step during componentization of non-targeted analysis (NTA) high-resolution mass spectrometry (HRMS) data, aiming to filter out false positive (FP) signals that do not belong to the component. Moreover, inclusion of FP fragments could lead to, for example, wrong identification further down the workflow. Commonly used methods for deconvolution of fragment signals rely on the presence of a time domain (e.g., peak apex retention time difference and correlation analysis). However, when there is no or insufficient MS2 information in the time domain, these methods are unusable and only the mass domain remains. A probability based cumulative neutral loss (CNL) model for fragment deconvolution using the mass domain information was thus developed to allow deconvolution for such cases. The optimized model, with a mass tolerance of 0.005 Da and a CNL score threshold of -0.95, was able to achieve true positive rate (TPr) of 95.0%, a false discovery rate (FDr) of 25.6%, and a reduction rate of 39.9%. Additionally, the CNL model was extensively tested on real samples containing predominantly pesticides at different concentration levels and with matrix effects. Overall, the model was able to obtain a TPr above 95% with FD rates between 45% and 77% and reduction rates between 10% and 24%. Finally, the CNL model was compared with the retention time difference method and peak shape correlation analysis, showing that a combination of correlation analysis and the CNL model was the most effective for fragment deconvolution, obtaining a TPr of 93.1%, a FDr of 57.2%, and a reduction rate of 42.6%.

Details

Database :
OpenAIRE
Accession number :
edsair.doi...........ca2af8528408b03277d5a6f930ddcaa5
Full Text :
https://doi.org/10.26434/chemrxiv-2023-vkq8q