Author

G. D. Campagnaro

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· 2 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:drug response / drug discovery· 1 Approach:mechanistic / dynamical model· 1

Frequent Co-Authors

J. C. Munday· 2 shared A. A. Eze· 1 shared A. Alghamdi· 1 shared A. Dimitriou· 1 shared A. K. Cruz· 1 shared A. Kumar· 1 shared A.-M. Donachie· 1 shared C. Dardonville· 1 shared

Activity by Year

2020-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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2 shared papersMicrobiology

J. C. Munday

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3 papers

Recent·Most cited

Genetic and functional dissection of the glutamate-proline pathway reveals a shortcut for glutamate catabolism in Leishmania

G. D. Campagnaro, A. K. Cruz

This study identifies a direct glutamate catabolism pathway in Leishmania, bypassing proline biosynthesis, and highlights differences in amino acid metabolism between Leishmania and Trypanosoma.

bioRxiv · Feb 6, 2024 · PreprintBiochemistry

Diminazene resistance in Trypanosoma congolense is linked to reduced mitochondrial membrane potential and not to reduced transport capacity

H. De Koning, L. V. Carruthers, J. C. Munday, G. U. Ebiloma, P. Steketee, S. Jayaraman, G. D. Campagnaro, M. A. Ungogo, A.-M. Donachie, T. G. Rowan, R. Peter, L. J. Morrison, M. P. Barrett

This study investigates diminazene resistance in Trypanosoma congolense and finds that resistance is due to reduced mitochondrial membrane potential rather than reduced drug transport capacity.

bioRxiv · Jul 28, 2020Microbiology

Positively selected modifications in the pore of TbAQP2 allow pentamidine to enter Trypanosoma brucei

A. Alghamdi, J. C. Munday, G. D. Campagnaro, D. Gurvic, F. Svensson, C. E. Okpara, A. Kumar, M. E. Martin Abril, P. Mili?, L. Watson, D. Paape, L. Settimo, A. Dimitriou, J. Wielinska, G. Smart, , H. P. De Koning

The paper identifies mutations in TbAQP2 that enable pentamidine permeation, showing how specific structural changes in the aquaporin pore allow drug entry in Trypanosoma brucei.

bioRxiv · Mar 8, 2020Biochemistry