Author

T. Stepniewski

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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Biophysics· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:host-pathogen & immune response· 1 Research Focus:protein folding & dynamics· 1

Frequent Co-Authors

A. K. Shukla· 2 shared E. Ghosh· 2 shared H. Dwivedi· 2 shared J. Selent· 2 shared M. Baidya· 2 shared P. Kumari· 2 shared S. Pandey· 2 shared A. Hanyaloglu· 1 shared

Activity by Year

2019-2019 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 43 mutual co-author links

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2 shared papersBiophysics

A. K. Shukla

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2 papers

Recent·Most cited

Conformational sensors and domain-swapping reveal structural and functional differences between β-arrestin isoforms

E. Ghosh, H. Dwivedi, M. Baidya, A. Srivastava, P. Kumari, T. Stepniewski, H. R. Kim, M.-H. Lee, J. v. Gastel, M. Chaturvedi, D. Roy, S. Pandey, J. Maharana, R. Guixa-Gonzalez, L. M. Luttrell, , A. K. Shukla

The paper identifies structural differences between β-arrestin isoforms using conformational sensors and domain-swapping, linking these differences to their distinct functional outcomes in GPCR signaling.

bioRxiv · Aug 5, 2019Biophysics

Genetically encoded intrabody sensors illuminate structural and functional diversity in GPCR-β-arrestin complexes

M. Baidya, P. Kumari, H. Dwivedi, E. Ghosh, B. Sokrat, S. Sposini, S. Pandey, T. Stepniewski, J. Selent, A. Hanyaloglu, M. Bouvier, A. K. Shukla

This study uses genetically encoded intrabody sensors to reveal structural and functional diversity in GPCR-β-arrestin complexes, showing distinct functional outcomes across different receptors.

bioRxiv · May 27, 2019 · PreprintCell Biology