Publications
82
Citations
1,495
Est. group size
—
Recurring co-author estimate
Active years
15
Publishing since 2012
Bryon Drown works in analytical and chemical biology, using mass spectrometry-based tools to study proteins in their full complexity, including modifications and variant forms (called proteoforms). Their work includes developing software and lab protocols for top-down proteomics (analyzing whole proteins rather than digested fragments), studying enzymes involved in protein degradation (deubiquitinases), and developing assays to find drug candidates such as SARS-CoV-2 macrodomain inhibitors. This research could interest students wanting to work at the interface of chemistry, mass spectrometry instrumentation, and biological questions like disease-related protein modifications.
Publication output rose sharply from 2017 to a peak around 2020-2021, then declined and has remained lower but steady from 2023 onward.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- HergenrotherLab/GramNegAccum: Publication v1.0
Open MIND · 2026
- HergenrotherLab/GramNegAccum: Publication v1.0
Zenodo (CERN European Organization for Nuclear Research) · 2026
- Protein Aggregation Capture for Top-down Proteomics
bioRxiv (Cold Spring Harbor Laboratory) · 2026
- Abstract 2013 Genetically encoded ubiquitin electrophiles for covalent trapping and inhibition of deubiquitinating enzymes
Journal of Biological Chemistry · 2025
- Internal Ubiquitin Electrophiles for Covalent Trapping and Inhibition of Deubiquitinases
ChemBioChem · 2025
- Temporal regulation of gene expression through integration of p53 dynamics and modifications
Science Advances · 2024
- MSModDetector: a tool for detecting mass shifts and post-translational modifications in individual ion mass spectrometry data
Bioinformatics · 2024
- Correction to “A Fluorescence Polarization Assay for Macrodomains Facilitates the Identification of Potent Inhibitors of the SARS-CoV-2 Macrodomain”
ACS Chemical Biology · 2024
- A Fluorescence Polarization Assay for Macrodomains Facilitates the Identification of Potent Inhibitors of the SARS-CoV-2 Macrodomain
ACS Chemical Biology · 2023
- Genetically Encoded Crosslinking Enables Identification of Multivalent Ubiquitin‐Deubiquitylating Enzyme Interactions
ChemBioChem · 2023
- MSModDetector: A Tool for Detecting Mass Shifts and Post-Translational Modifications in Individual Ion Mass Spectrometry Data
bioRxiv (Cold Spring Harbor Laboratory) · 2023
- Proteoforms feel the heat
Nature Chemical Biology · 2023
- Mapping the Proteoform Landscape of Five Human Tissues
Journal of Proteome Research · 2022
- Mapping the KRAS proteoform landscape in colorectal cancer identifies truncated KRAS4B that decreases MAPK signaling
Journal of Biological Chemistry · 2022
- Mapping the Proteoform Landscape of Five Human Tissues
ChemRxiv · 2022
- bioRxiv (Cold Spring Harbor Laboratory)×4
- Science Advances×2
- Journal of Biological Chemistry×2
- Cell chemical biology×2
- ACS Chemical Biology×2
- Brian C. Searle
Chemistry · The Ohio State University
- Sujun Li
Chemistry · Indiana University
- Joseph Fernandez
Chemistry · The Ohio State University
- Jonathan C. Trinidad
Chemistry · Indiana University
- Arbil Lopez
Chemistry · The Ohio State University
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 20, 2026.
Claim or correct this profile