Author

F. Trovato

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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Research Focus:protein folding & dynamics· 2 Approach:deep learning· 1 Organism:E. coli· 1 Assay:protein structure· 1 Approach:statistical model· 1

Frequent Co-Authors

D. A. Nissley· 2 shared E. P. O'Brien· 2 shared I. Sitarik· 1 shared K. Narayan· 1 shared P. To· 1 shared S. D. Fried· 1 shared S. E. Leininger· 1 shared Y. Jiang· 1 shared

Activity by Year

2018-2021 · peak 1/yr

Co-Author Collaboration Network

9 top collaborators · 30 mutual co-author links

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2 shared papersBiochemistry

D. A. Nissley

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2 papers

Recent·Most cited

Universal protein misfolding intermediates can bypass the proteostasis network and remain soluble and less-functional

D. A. Nissley, Y. Jiang, F. Trovato, I. Sitarik, K. Narayan, P. To, Y. Xia, S. D. Fried, E. P. O'Brien

The paper shows that misfolded proteins can bypass proteostasis by being structurally similar to native states and persisting for long periods.

bioRxiv · Aug 18, 2021Biochemistry

Domain topology, stability, and translation speed determine mechanical force generation on the ribosome

S. E. Leininger, F. Trovato, D. A. Nissley, E. P. O'Brien

This study shows that mechanical forces on ribosomes during translation depend on domain stability, topology, and translation speed, with implications for protein structure and evolution.

bioRxiv · Dec 7, 2018Biophysics