Author

C. R. Corona

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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Biochemistry· 1 Cancer Biology· 1 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Research Focus:drug response / drug discovery· 3 Approach:experimental assay· 3 Organism:human· 2 Assay:proteomics· 2 Assay:protein structure· 1

Frequent Co-Authors

J. D. Vasta· 3 shared C. A. Zimprich· 2 shared M. B. Robers· 2 shared M. T. Beck· 2 shared A. Lewis· 1 shared A. Michaud· 1 shared A. Schwarzenstein· 1 shared B. F. Binkowski· 1 shared

Activity by Year

2022-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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3 shared papersPharmacology & Toxicology

J. D. Vasta

Mutual co-authors in cluster

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3 papers

Recent·Most cited

Pharmacology & ToxicologybioRxivPreprintNov 11, 2026

Denaturation-sensitive BRET probes enable intracellular thermal shift measurements across diverse protein targets and biomolecular complexes

J. D. Vasta, A. Michaud, M. T. Beck…·Matthew B. Robers

This paper introduces BRETSA, a method for measuring thermal shifts in living cells, and demonstrates its application across 500+ proteins and biomolecular complexes.

DOI 10.64898/2026.11.10.765695

protein structureexperimental assay

𝕏 PostBluesky

BiochemistrybioRxivPreprintMar 22, 2022

Small Molecule Modulation of the Archetypal UbiB protein COQ8

N. H. Murray, A. Lewis, C. R. M. Asquith…·D. J. Pagliarini

The paper develops small molecule inhibitors and activators for COQ8A, a UbiB family protein, using crystallography, NMR, and mass spectrometry to modulate its function in CoQ biosynthesis.

DOI 10.1101/2022.03.22.485346

humanproteomics

𝕏 PostBluesky

Cancer BiologyNature Chemical BiologyPeer-reviewedMar 21, 2022

KRAS is vulnerable to reversible switch-II pocket engagement in cells

J. D. Vasta, D. M. Peacock, Q. Zheng…·K. M. Shokat

The paper investigates the accessibility of the switch-II pocket in various KRAS mutants using NMR and a cellular engagement assay, showing it is accessible with non-covalent ligands regardless of GDP state.

DOI 10.1038/s41589-022-00985-w

humanproteomics

𝕏 PostBluesky