Author

M. R. Stoneman

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· 2

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

G. Biener· 2 shared V. Raicu· 2 shared D. N. Badu· 1 shared G. Milligan· 1 shared I. V. Popa· 1 shared J. D. Paprocki· 1 shared J. D. Pediani· 1 shared R. J. Ward· 1 shared

Activity by Year

2018-2020 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 23 mutual co-author links

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2 shared papersBiophysics

G. Biener

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2 papers

Recent·Most cited

In-cell detection of conformational sub-states of a GPCR quaternary structure: Modulation of sub-state probability by cognate ligand binding

J. D. Paprocki, G. Biener, M. R. Stoneman, V. Raicu

This study improves FRET spectrometry to detect conformational sub-states of GPCR oligomers and shows ligand binding modulates these sub-states in Ste2.

bioRxiv · Jun 29, 2020Biophysics

A general method to quantify ligand-driven oligomerization using single- or two-photon excitation microscopy

M. R. Stoneman, G. Biener, R. J. Ward, J. D. Pediani, D. N. Badu, I. V. Popa, G. Milligan, V. Raicu

This paper introduces a method to quantify ligand-driven oligomerization using fluorescence intensity fluctuation spectrometry with single- or two-photon excitation microscopy, showing it can detect oligomer size and stability in membrane proteins.

bioRxiv · Nov 23, 2018 · PreprintBiophysics