Author

T. W. McCullock

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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Biophysics· 1 Pharmacology & Toxicology· 1 Physiology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 3 Approach:experimental assay· 2 Assay:fluorescence / live-cell microscopy· 2 Research Focus:cell type annotation· 1 Organism:human· 1 Approach:microscopy & imaging analysis· 1

Frequent Co-Authors

D. M. MacLean· 2 shared P. J. Kammermeier· 2 shared D. L. Kneisley· 1 shared K. Berger· 1 shared L. P. Cardani· 1 shared P. Kammermeier· 1 shared T. Couch· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

7 top collaborators · 12 mutual co-author links

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2 shared papersPhysiology

D. M. MacLean

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Author profile →

3 papers

Recent·Most cited

Signaling specificity and kinetics of the human metabotropic glutamate receptors.

T. W. McCullock, L. P. Cardani, P. J. Kammermeier

This study examines the G protein coupling profiles of all human mGluR homodimers using a BRET assay, revealing unexpected coupling patterns beyond canonical expectations.

bioRxiv · Jul 24, 2023Pharmacology & Toxicology

Topography and motion of the acid-sensing ion channel intracellular domains

T. Couch, K. Berger, D. L. Kneisley, T. W. McCullock, P. J. Kammermeier, D. M. MacLean

This study uses FRET to map the topography and motion of ASIC1 intracellular domains, revealing structural features and conformational changes under acidification.

bioRxiv · Feb 23, 2021Physiology

Comparing the performance of mScarlet-I, mRuby3, and mCherry as FRET acceptors for mNeonGreen

T. W. McCullock, D. M. MacLean, P. Kammermeier

This study compares mScarlet-I, mRuby3, and mCherry as FRET acceptors for mNeonGreen, finding mScarlet-I and mCherry effective while mRuby3 performs poorly.

bioRxiv · Jul 5, 2019Biophysics