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Xing, Shipei

University of British Columbia

Metabolomics is an emerging omics study that aims to characterize the entire metabolome in a biological system. Mass spectrometry (MS) is a preferred analytical technique for metabolomics research owing to its high sensitivity and highly specific structural information content. However, it remains a longstanding challenge to accurately translate MS signals into chemical language, thus hindering the downstream biological interpretation. This dissertation presents computational strategies contributing to tandem mass (MS/MS) spectral interpretations with the aid of machine learning and statistical approaches. Chapter 1 provides a holistic introduction to MS-based metabolomics and the developed bioinformatic tools for uncovering the unidentified metabolic features in untargeted metabolomics. Chapter 2 describes a novel MS/MS spectral comparison algorithm, Core Structure-based Search (CSS), which searches for structural analogs of unknown MS/MS spectra within the existing MS/MS reference libraries. CSS shows improved correlations with structural similarity in large-scale benchmarking. In Chapter 3, a deep learning-based tool is developed for automated extraction of steroid-like metabolic features from the untargeted metabolomics data by classifying MS/MS fragmentation patterns. This biology-driven metabolomics pipeline enables metabolite characterization and discovery on the compound class level. Chapter 4 depicts the purification of chimeric MS/MS spectra using a random forest model. Purified MS/MS spectra are demonstrated to yield better spectral matching results against MS/MS reference libraries. Chapter 5 describes the systematic analysis of radical fragment ions in MS/MS through MS/MS database mining. Larger than expected percentages of radical ions are present in collision- induced dissociation-based MS/MS; relationships between radical ion percentages and compound classes, chemical substructures and collision energies are also investigated. Chapter 6 discusses a standalone platform, BUDDY, for molecular formula discovery via bottom-up MS/MS interrogation and experiment-specific global peak annotation. BUDDY further integrates machine-learned ranking and significance control, showing improved formula annotation accuracy and lower computational cost than other benchmarking tools. Applying BUDDY on repository- scale recurrent unidentified MS/MS spectra, we discovered >5,000 chemical database-unarchived molecular formulae with high confidence. Overall, this dissertation demonstrates computational contributions to enriching structural insights into MS-based untargeted metabolomics data, thus paving the way for understanding biological mechanisms behind various health disorders and diseases from the perspective of small molecules.

Text

2023-04-20

Attribution-NonCommercial-NoDerivatives 4.0 International

http://hdl.handle.net/2429/84373

Chemistry

University of British Columbia

UBCV

http://creativecommons.org/licenses/by-nc-nd/4.0/