Author

Sarah E.J. Morf

Monash UniversityORCID 0009-0002-8260-6534Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:development & morphogenesis· 1 Organism:human· 1 Assay:proteomics· 1

Frequent Co-Authors

Alice J. SharpeiD· 2 shared Kate McArthuriD· 2 shared Luke E. FormosaiD· 2 shared Matthew P. ChallisiD· 2 shared Michael T. RyaniD· 2 shared Caitlin L. RoweiD· 1 shared Matthew J. EramoiD· 1 shared Natasha Kapoor-Kaushik· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersCell Biology

Alice J. SharpeORCID

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2 papers

Recent·Most cited

Proximity labelling of the BAK macropore uncovers a new role for SLC35A4-MP in mitochondrial dynamics

Matthew P. Challis, Stephanie M. Molé, Saveen Giri, Ryker Dumbrill, Matthew J. Eramo, Alice J. Sharpe, Sarah E.J. Morf, Kate McArthur, Luke E. Formosa, Michael T. Ryan

This study uses proximity labeling to identify proteins near the BAK pore during apoptosis, revealing SLC35A4-MP's role in modulating mitochondrial dynamics.

bioRxiv · Mar 24, 2026 · PreprintCell Biology

Characterization of human Metaxin proteins reveals functional diversification of SAM37 homologs MTX1 and MTX3

Sarah E.J. Morf, Matthew P. Challis, Sanjeev Uthishtran, Caitlin L. Rowe, Alice J. Sharpe, Natasha Kapoor-Kaushik, Senthil Arumugam, Luke E. Formosa, Kate McArthur, Michael T. Ryan

This study investigates the functional differences between MTX1 and MTX3, showing that their loss leads to distinct mitochondrial phenotypes and that both depend on MTX2 for stability.

bioRxiv · Mar 17, 2026 · PreprintBiochemistry