Author

D. P. Staus

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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Cell Biology· 1 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:drug response / drug discovery· 1 Organism:human· 1

Frequent Co-Authors

A. C. Kruse· 1 shared A. Inoue· 1 shared A. W. Kahsai· 1 shared C. Lee· 1 shared C. McMahon· 1 shared G. R. Nemeth· 1 shared H. Xu· 1 shared I. Choi· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperPharmacology & Toxicology

A. C. Kruse

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2 papers

Recent·Most cited

Antibodies Expand the Scope of Angiotensin Receptor Pharmacology

M. A. Skiba, S. M. Sterling, S. Rawson, M. S. A. Gilman, H. Xu, G. R. Nemeth, J. D. Hurley, P. Shen, D. P. Staus, J. Kim, C. McMahon, M. K. Lehtinen, L. M. Wingler, A. C. Kruse

This study develops nanobody antagonists against the AT1R receptor, showing they can selectively bind and modulate the receptor with tunable ligand selectivity.

bioRxiv · Aug 23, 2023Pharmacology & Toxicology

Noncanonical scaffolding of Gαi and β-arrestin by G protein-coupled receptors

J. S. Smith, T. F. Pack, A. Inoue, C. Lee, X. Xiong, K. Zheng, A. W. Kahsai, I. Choi, Z. Ma, I. M. Levitan, L. K. Rochelle, D. P. Staus, J. C. Snyder, M. G. Caron, S. Rajagopal

The paper demonstrates that Gαi proteins can form complexes with β-arrestin, independent of their canonical G protein coupling, and these complexes can bind GPCRs and ERK.

bioRxiv · May 7, 2019Cell Biology