Author

L. Fornelli

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 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Assay:proteomics· 2 Research Focus:cell type annotation· 1 Organism:mouse· 1 Research Focus:protein folding & dynamics· 1

Frequent Co-Authors

A. H. Rowe· 1 shared A. Heaston· 1 shared D. R. Rokyta· 1 shared H. Gridley· 1 shared J. D. Stockand· 1 shared J. Kline· 1 shared J. P. McGee· 1 shared K. D. Linse· 1 shared

Activity by Year

2019-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperPharmacology & Toxicology

A. H. Rowe

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2 papers

Recent·Most cited

Identification and characterization of novel proteins from Arizona bark scorpion venom that inhibit Nav1.8, a voltage-gated sodium channel regulator of pain signaling

T. M. Abd El-Aziz, Y. Xiao, J. Kline, H. Gridley, A. Heaston, K. D. Linse, M. J. Ward, D. R. Rokyta, J. D. Stockand, T. R. Cummins, L. Fornelli, A. H. Rowe

The paper identifies four novel scorpion venom proteins that inhibit Nav1.8, a sodium channel involved in pain signaling, through proteomic and electrophysiological analyses.

bioRxiv · Jun 24, 2021Pharmacology & Toxicology

Direct Measurement of Light and Heavy Antibody Chains Using Differential Ion Mobility Spectrometry and Middle-Down Mass Spectrometry

R. D. Melani, K. Srzentic, V. R. Gerbasi, J. P. McGee, R. Huguet, L. Fornelli, N. L. Kelleher

This paper introduces a rapid FAIMS tandem MS method for characterizing monoclonal antibody light and heavy chains, reducing analysis time by 40-60% compared to LC-MS/MS.

bioRxiv · Jul 5, 2019Biochemistry