Author

Camille Sullivan

Howard Hughes Medical InstituteORCID 0000-0002-2175-4288Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Biophysics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Organism:Drosophila· 1 Approach:experimental assay· 1 Organism:human· 1 Research Focus:protein design· 1 Research Focus:protein folding & dynamics· 1 Research Focus:protein structure prediction· 1 Assay:proteomics· 1

Frequent Co-Authors

Dorothee KerniD· 2 shared Adedolapo M. OjoawoiD· 1 shared Andrew GlaseriD· 1 shared E. Nicholas PeterseniD· 1 shared Evelyn KeeferiD· 1 shared Hannes LudewigiD· 1 shared Michael RosbashiD· 1 shared R.A.P. PaduaiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 16 mutual co-author links

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2 shared papersBiophysics

Dorothee KernORCID

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2 papers

Recent·Most cited

Phosphatase SHP2 pathogenic mutations enhance activity by altering conformational sampling

Andrew Glaser, R.A.P. Padua, Adedolapo M. Ojoawo, Camille Sullivan, Dorothee Kern

This study investigates how pathogenic mutations in SHP2's SH2 domains alter conformational dynamics, leading to hyperactivation by stabilizing a zipped β-sheet state.

Proceedings of the National Academy of Sciences · Jan 13, 2026Peer-reviewedBiophysics

The dramatic impact of the PER-DBT interaction on circadian timekeeping and temperature compensation

E. Nicholas Petersen, Evelyn Keefer, Hannes Ludewig, Camille Sullivan, Dorothee Kern, Michael Rosbash

The paper identifies a conserved PER-DBT interaction critical for circadian timing and temperature compensation through structural and functional analyses in Drosophila and human cells.

bioRxiv · Feb 1, 2025 · PreprintMolecular Biology