Author

Emma E. Drew

University of OregonORCID 0000-0001-9409-683XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 2 Approach:experimental assay· 2 Organism:human· 2 Assay:fluorescence / live-cell microscopy· 1 Assay:proteomics· 1

Frequent Co-Authors

Scott D. HanseniD· 2 shared Althea Amaris· 1 shared Asa J. Noteboom· 1 shared Grace L. WaddelliD· 1 shared Hunter G. NyvalliD· 1 shared John E. BurkeiD· 1 shared Matthew AH ParsoniD· 1 shared Reed K. Talus· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersCell Biology

Scott D. HansenORCID

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2 papers

Recent·Most cited

SHIP1 partitions between cortical oscillations and membrane puncta to regulate neutrophil chemotaxis

Althea Amaris, Grace L. Waddell, Asa J. Noteboom, Sophia Doerr, Emma E. Drew, Sean R. Collins, Scott D. Hansen

This study identifies two SHIP1 localization modes during neutrophil chemotaxis, regulated by FBP17 and Nck1, and shows that the C-terminal domain is essential for proper chemotaxis.

bioRxiv · May 28, 2026 · PreprintCell Biology

SH2-mediated steric occlusion of the C2 domain regulates autoinhibition of SHIP1 inositol 5-phosphatase

Emma E. Drew, Hunter G. Nyvall, Matthew AH Parson, Reed K. Talus, John E. Burke, Scott D. Hansen

This study identifies how the SH2 domain sterically occludes the C2 domain to autoinhibit SHIP1, revealing structural and functional relationships critical for its membrane localization and phosphatase activity.

Journal of Biological Chemistry · Oct 7, 2025Peer-reviewedBiochemistry