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Toward Machine Learning Electrospray Ionization Sensitivity Prediction for Semiquantitative Lipidomics in Stem Cells
Alexandria Van Grouw1, Markace A Rainey1, Olivia K Reid1
1School of Chemistry and Biochemistry, Georgia Institute of Technology, 901 Atlanta Drive, Atlanta, Georgia 30332, USA.
Journal of Chemical Information and Modeling
|February 5, 2025
Summary
A new machine learning model predicts electrospray ionization sensitivity for lipids, enabling semi-quantitative lipidomics in multiyear stem cell studies. This approach overcomes batch-to-batch variability without requiring costly chemical standards.
Area of Science:
- Analytical Chemistry
- Biochemistry
- Data Science
Background:
- Mass spectrometry (MS) is crucial for metabolomics and lipidomics but faces challenges in multiyear, multi-batch studies due to electrospray ionization (ESI) response variability.
- This variability hinders accurate batch-to-batch comparisons, creating a divide between broad discovery work and scope-limited targeted quantitation.
Purpose of the Study:
- To develop a machine learning (ML) model for predicting ESI sensitivity of lipid classes relevant to stem cell potency.
- To enable semi-quantitation of lipids across batches in long-term stem cell studies, bridging the gap between discovery and targeted approaches.
Main Methods:
- Utilized molecular descriptors from lipid chemical structures as input for an ML model to predict ESI response.
- Validated the model using cultured stem cell samples from diverse donors, assessing performance in both positive and negative ion modes.
Main Results:
- The ML model achieved moderate accuracy (global percent errors of 40% for positive and 20% for negative modes), sufficient for semi-quantitation.
- Demonstrated high precision (16.9% positive, 7.5% negative modes), indicating potential for data harmonization across batches.
- The chosen molecular descriptors improved accuracy compared to previous literature.
Conclusions:
- The developed ML model effectively predicts ESI sensitivity, enabling semi-quantitative lipidomics in challenging multi-batch stem cell research.
- This approach offers a viable solution for lipid marker concentration estimation across batches without reliance on unavailable isotopic standards.
- The findings show significant promise for advancing data harmonization and quantitative capabilities in lipidomics.

