Andrew Erickson
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Andrew Erickson has a total of 3 co-authors. Here are the top co-authors by number of shared publications:
Natalie Ito
Yale University
1 shared publication- Xiaoai Zhao
Department of Genetics, Stanford University, Stanford, CA, USA
1 shared publication - Zixing Chen
Yale University
1 shared publication
Latest Publications
- Open Access
RISOP, a Reference-Assisted Approach for Enhanced Identification of Oxidized Phospholipids
Oxidized phospholipids (OxPLs) play critical roles in inflammation, ferroptosis, and other oxidative stress-associated processes, yet their systematic characterization in biological systems remains a major analytical challenge owing to their low abundance and vast structural diversity. Here we report RISOP (Reference-Assisted Identification of Sample-specific Oxidized Phospholipids), an untargeted LC-MS/MS workflow that leverages chemically enriched OxPL reference pools to substantially improve OxPL annotation. Reference pools encompassing diverse oxidative modifications and a wide abundance range were experimentally generated using Fenton reaction and H2O2 treatment, providing broad coverage of OxPLs. Reference-assisted integrative analysis yielded a more than twofold increase in identified OxPL species in biological samples under elevated oxidative stress, as demonstrated in ML210-treated cells, a model of ferroptotic stress. We further show that the widely used BODIPY C11 lipid peroxidation probe captures cellular oxidative burden in only a subset of OxPLs identified by RISOP, highlighting the importance of untargeted, comprehensive OxPL profiling. Overall, RISOP provides a versatile platform readily applicable to other classes of oxidized complex lipids for comprehensive characterization in physiological and pathological contexts.
Open AccessRISOP, a Reference-Assisted Approach for Enhanced Identification of Oxidized Phospholipids
Oxidized phospholipids (OxPLs) play critical roles in inflammation, ferroptosis, and other oxidative stress-associated processes, yet their systematic characterization in biological systems remains a major analytical challenge owing to their low abundance and vast structural diversity. Here we report RISOP (Reference-Assisted Identification of Sample-specific Oxidized Phospholipids), an untargeted LC-MS/MS workflow that leverages chemically enriched OxPL reference pools to substantially improve OxPL annotation. Reference pools encompassing diverse oxidative modifications and a wide abundance range were experimentally generated using Fenton reaction and H2O2 treatment, providing broad coverage of OxPLs. Reference-assisted integrative analysis yielded a more than twofold increase in identified OxPL species in biological samples under elevated oxidative stress, as demonstrated in ML210-treated cells, a model of ferroptotic stress. We further show that the widely used BODIPY C11 lipid peroxidation probe captures cellular oxidative burden in only a subset of OxPLs identified by RISOP, highlighting the importance of untargeted, comprehensive OxPL profiling. Overall, RISOP provides a versatile platform readily applicable to other classes of oxidized complex lipids for comprehensive characterization in physiological and pathological contexts.