Author

D. T. Gallagher

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· 2 Bioengineering· 1 Biophysics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Research Focus:protein folding & dynamics· 3 Assay:protein structure· 2 Assay:proteomics· 2 Research Focus:drug response / drug discovery· 1 Organism:human· 1

Frequent Co-Authors

B. Ruan· 3 shared D. Motabar· 3 shared E. J. Choi· 3 shared P. N. Bryan· 3 shared R. Simmerman· 3 shared Y. Chen· 3 shared Y. He· 3 shared J. Orban· 2 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersBiochemistry

B. Ruan

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Author profile →

4 papers

Recent·Most cited

Detecting Features of Protein Structure through their Mediator-Accessible Redox Activities

D. Motabar, E. Kim, J. Li, Z. Zhao, T. Mouchahoir, D. T. Gallagher, J. E. Schiel, M. Garige, C. Sourbier, G. F. Payne, W. E. Bentley

This paper introduces an electronic detection method to identify structural perturbations in proteins by measuring mediator-accessible redox activities, demonstrating its application in biomanufacturing.

bioRxiv · Dec 12, 2023 · PreprintBioengineering

Design and characterization of a protein fold switching network

B. Ruan, Y. He, Y. Chen, E. J. Choi, Y. Chen, D. Motabar, T. Solomon, R. Simmerman, T. Kauffman, D. T. Gallagher, J. P. Orban, P. N. Bryan

The paper designs and characterizes a protein fold switching network where single amino acid substitutions can switch fold and function in proteins.

bioRxiv · Oct 26, 2022Biochemistry

Rules for designing protein fold switches and their implications for the folding code

Y. Chen, Y. He, B. Ruan, E. J. Choi, Y. Chen, D. Motabar, T. Solomon, R. Simmerman, T. Kauffman, D. T. Gallagher, J. Orban, P. N. BRYAN

The paper designs protein fold switches between three common small folds and identifies rules for engineering dimorphic sequences that can populate multiple folds.

bioRxiv · May 18, 2021 · PreprintBiophysics

Engineering protein-specific proteases: targeting active RAS

Y. Chen, E. A. Toth, B. Ruan, E. J. Choi, R. Simmerman, Y. Chen, Y. He, R. Wang, R. Godoy-Ruiz, H. King, G. Custer, D. T. Gallagher, D. A. Rozak, M. Soloman, S. Muro, , P. N. Bryan

This study designs engineered proteases that specifically degrade active RAS by cleaving a conserved sequence in switch 2, showing efficacy in vitro and in human cell culture.

bioRxiv · Sep 21, 2020Biochemistry