Author

M. T. Halma

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 Biophysics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Organism:mouse· 1 Assay:proteomics· 1 Organism:rat· 1

Frequent Co-Authors

M. T. Woodside· 2 shared C. F. Halpern· 1 shared D. B. Ritchie· 1 shared J. A. Kelly· 1 shared J. D. Dinman· 1 shared K. Neupane· 1 shared S. Loerch· 1 shared S. M. Ileperuma· 1 shared

Activity by Year

2020-2021 · peak 1/yr

Co-Author Collaboration Network

9 top collaborators · 29 mutual co-author links

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2 shared papersBiochemistry

M. T. Woodside

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2 papers

Recent·Most cited

Small-molecule ligands can inhibit -1 programmed ribosomal frameshifting in a broad spectrum of coronaviruses

S. Munshi, K. Neupane, S. M. Ileperuma, M. T. Halma, J. A. Kelly, C. F. Halpern, J. D. Dinman, S. Loerch, M. T. Woodside

The paper tests small-molecule ligands against -1 PRF in coronaviruses, finding nafamostat inhibits frameshifting in multiple bat CoVs and SARS-CoV-2 but not other viruses.

bioRxiv · Aug 6, 2021 · PreprintBiochemistry

Conformational Shannon entropy of mRNA structures from force spectroscopy measurements predicts the efficiency of -1 programmed ribosomal frameshift stimulation

M. T. Halma, D. B. Ritchie, M. T. Woodside

The paper shows that -1 PRF efficiency correlates with the conformational heterogeneity of mRNA structures, measured as Shannon entropy, and this correlation depends on force.

bioRxiv · Dec 12, 2020Biophysics