Author

S. C. Charnaud

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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Microbiology· 2

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

B. S. Crabb· 2 shared H. E. Bullen· 2 shared P. R. Gilson· 2 shared B. Elsworth· 1 shared M. G. Dans· 1 shared M. Gabriela· 1 shared M. McConville· 1 shared M. Parkyn Schneider· 1 shared

Activity by Year

2018-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersMicrobiology

B. S. Crabb

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2 papers

Recent·Most cited

PTEX helps efficiently traffic haemoglobinases to the food vacuole in Plasmodium falciparum.

T. K. Jonsdottir, B. Elsworth, S. Cobbold, M. Gabriela, S. C. Charnaud, M. G. Dans, M. Parkyn Schneider, M. McConville, H. E. Bullen, B. S. Crabb, P. R. Gilson

This study identifies PTEX150 as essential for trafficking haemoglobinases to the food vacuole in Plasmodium falciparum, revealing a new metabolic function for PTEX beyond the known permeability pathway.

bioRxiv · Nov 15, 2022 · PreprintMicrobiology

Knockdown of the translocon protein EXP2, reduces growth and protein export in malaria parasites.

P. R. Gilson, S. C. Charnaud, R. Kumarasingha, H. E. Bullen, B. S. Crabb

This study shows that knocking down EXP2 in malaria parasites reduces growth and protein export, suggesting EXP2 is essential for the PTEX translocon's function in exporting proteins into host cells.

bioRxiv · Sep 17, 2018Microbiology