Author

Philipp Dahlhaus

Philipps University of Marburg

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

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Assay:cryo-EM· 1 Research Focus:drug response / drug discovery· 1 Organism:human· 1 Assay:metabolomics· 1 Research Focus:protein folding & dynamics· 1

Frequent Co-Authors

Daniel HilgeriD· 2 shared Achilleas S. FrangakisiD· 1 shared Amira NaimiiD· 1 shared Anja Seybert· 1 shared Anna Grimm· 1 shared Daniel PetrasiD· 1 shared Evi KostenisiD· 1 shared Felipe MerinoiD· 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 papersBiochemistry

Daniel HilgerORCID

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2 papers

Recent·Most cited

Discovery of a Cell-Permeable Gi-Signaling Inhibitor

Amira Naimi, Tim Berger, Philipp Dahlhaus, Marcel Rossol, Jonas Mühle, Wieland Steinchen, Gert Bange, Uwe Linne, Paolo Stincone, Xavier Deupí, Gebhard F. X. Schertler, Lars Jürgenliemke, Evi Kostenis, Jens Kockskämper, Daniel Hilger, , Raphael Reher

This paper discovers NHAP, a fungal metabolite that selectively inhibits Gi-signaling, demonstrating functional blockade in cardiomyocytes without cytotoxicity.

bioRxiv · Aug 4, 2026 · PreprintBiochemistry

Cryo-EM structure of a cell-free synthesized full-length human β1-adrenergic receptor in complex with Gs

Felipe Merino, Zoe Köck, Utz H. Ermel, Philipp Dahlhaus, Anna Grimm, Anja Seybert, Jan Kubicek, Achilleas S. Frangakis, Volker Dötsch, Daniel Hilger, Frank Bernhard

The paper determines the cryo-EM structure of a full-length human β1-adrenergic receptor in complex with Gs, revealing structural insights into ICL3's role in G protein activation.

Structure · Aug 25, 2025Peer-reviewedBiochemistry