Author

W. D. Barshop

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Cell Biology· 1 Microbiology· 1 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Assay:proteomics· 2 Research Focus:benchmarking· 1 Approach:deep learning· 1 Research Focus:drug response / drug discovery· 1 Research Focus:host-pathogen & immune response· 1 Research Focus:metabolism & bioenergetics· 1

Frequent Co-Authors

J. Canterbury· 2 shared A. J. Berk· 1 shared A. M. Robitaille· 1 shared B. Bills· 1 shared C. D. McGann· 1 shared C. Lin· 1 shared D. K. Schweppe· 1 shared E. Hsu· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 16 mutual co-author links

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2 shared papersCell Biology

J. Canterbury

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Author profile →

3 papers

Recent·Most cited

Real-time spectral library matching for sample multiplexed quantitative proteomics.

C. D. McGann, W. D. Barshop, J. Canterbury, C. Lin, W. Gabriel, M. Wilhelm, G. McAlister, D. K. Schweppe

This paper introduces a real-time library searching workflow to improve quantitation in sample multiplexed proteomics by enabling intelligent scan triggering and peak selection.

bioRxiv · Feb 8, 2023Cell Biology

Novel Real-Time Library Search driven data acquisition strategy for identification and characterization of metabolites.

B. Bills, W. D. Barshop, S. Sharma, J. Canterbury, A. M. Robitaille, M. W. Senko, V. Zabrouskov

The paper introduces a real-time data acquisition strategy, Met-IQ, that improves metabolite identification by selectively triggering MS3 scans based on spectral similarity, resulting in 55% more unique metabolite identifications.

bioRxiv · Oct 7, 2021Pharmacology & Toxicology

Adenovirus E1A Binding to DCAF10 Targets Degradation of AAA+ ATPases Required for Quaternary Assembly of Multiprotein Machines and Innate Immunity

N. R. Zemke, W. D. Barshop, J. Sha, E. Hsu, J. A. Wohlschlegel, A. J. Berk

The paper identifies that adenovirus E1A's C-terminal region interacts with host proteins to form a complex that degrades AAA+ ATPases, thereby inhibiting IRF3 stabilization and innate immune responses.

bioRxiv · Dec 16, 2020 · PreprintMicrobiology