Author

Verena Nadin Fritsch

Osnabrück UniversityORCID 0000-0002-7598-6754Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Approach:deep learning· 1 Approach:experimental assay· 1 Assay:fluorescence / live-cell microscopy· 1 Research Focus:host-pathogen & immune response· 1 Research Focus:protein folding & dynamics· 1

Frequent Co-Authors

Agnieszka K. BronowskaiD· 1 shared Antonia Kern· 1 shared Daniil BaranoviD· 1 shared Fabiana BurchertiD· 1 shared Gert BangeiD· 1 shared Haike AntelmanniD· 1 shared Michael HenseliD· 1 shared Michael HoltmannspötteriD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperMicrobiology

Agnieszka K. BronowskaORCID

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2 papers

Recent·Most cited

Improved HaloTag for analyses of translocation of type III secretion system effector proteins

Verena Nadin Fritsch, Michael Holtmannspötter, Michael Hensel

The paper introduces an improved HaloTag variant, HT-SP5, that enables more sensitive and earlier detection of T3SS-translocated effector proteins in living cells.

bioRxiv · Jun 1, 2026 · PreprintMicrobiology

Structural basis of quinone-sensing by the MarR-type repressor MhqR in Staphylococcus aureus

Thao Thi-Phuong Nguyen, Paul Stanley Weiland, Vu Van Loi, Stephan Kiontke, Fabiana Burchert, Victor Zegarra, Antonia Kern, Verena Nadin Fritsch, Daniil Baranov, Agnieszka K. Bronowska, Gert Bange, Haike Antelmann

This paper identifies the quinone-binding pocket of SaMhqR and elucidates its mechanism of inactivation through structural and mutational analyses.

mBio · Dec 31, 2025Peer-reviewedMicrobiology