Author

T. F. Gunnels

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Bioengineering· 2 Biophysics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 3 Research Focus:host-pathogen & immune response· 2 Research Focus:drug response / drug discovery· 1 Organism:E. coli· 1 Assay:electrophysiology· 1 Approach:mechanistic / dynamical model· 1 Organism:mouse· 1

Frequent Co-Authors

N. Kamat· 3 shared J. N. Leonard· 2 shared A. Lemley· 1 shared D. Baker· 1 shared D. M. Stranford· 1 shared H. I. Edelstein· 1 shared J. A. Peruzzi· 1 shared J. Steinkühler· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

3 shared papersBioengineering

N. Kamat

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Enhancing extracellular vesicle cargo loading and functional delivery by engineering protein-lipid interactions

J. A. Peruzzi, T. F. Gunnels, H. I. Edelstein, P. Lu, D. Baker, J. N. Leonard, N. Kamat

This study shows how engineering protein-lipid interactions can improve the loading and delivery of protein cargo into extracellular vesicles for therapeutic applications.

bioRxiv · Apr 29, 2023 · PreprintBioengineering

Probing the force-from-lipid mechanism with synthetic polymers

M. L. Jacobs, J. Steinkühler, A. Lemley, M. J. Larmore, T. F. Gunnels, L. C. T. Ng, S. M. Cologna, P. G. DeCaen, N. Kamat

This study investigates how changes in membrane mechanical properties affect the activation of mechanosensitive channels using synthetic amphiphiles and molecular dynamics simulations.

bioRxiv · May 20, 2022 · PreprintBiophysics

Elucidating design principles for engineering cell-derived vesicles to inhibit SARS-CoV-2 infection

T. F. Gunnels, D. M. Stranford, R. E. Mitrut, N. Kamat, J. N. Leonard

This study evaluates cell-derived vesicles as decoy nanoparticles to inhibit SARS-CoV-2 infection, finding they are effective against multiple variants and manufacturing methods.

bioRxiv · Dec 4, 2021Bioengineering