Author

R. Buschauer

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 Biophysics· 1

Signature Assays, Organisms & Methods

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Assay:cryo-EM· 2 Approach:experimental assay· 2 Approach:microscopy & imaging analysis· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:chromatin & epigenetic regulation· 1 Assay:CUT&Tag· 1 Organism:human· 1 Research Focus:protein folding & dynamics· 1

Frequent Co-Authors

O. Berninghausen· 2 shared R. Beckmann· 2 shared A. R. Buskirk· 1 shared C. C.-C. Wu· 1 shared D. Boassa· 1 shared E. Hurt· 1 shared E. Villa· 1 shared J. Boehning· 1 shared

Activity by Year

2019-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

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2 shared papersBiochemistry

O. Berninghausen

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Concurrent remodelling of nucleolar 60S subunit precursors by the Rea1 ATPase and Spb4 RNA helicase

V. Mitterer, M. Thoms, R. Buschauer, O. Berninghausen, E. Hurt, R. Beckmann

This study shows how Rea1 ATPase and Spb4 helicase work together to remodel pre-60S ribosomal particles by restructuring rRNA and removing assembly factors.

bioRxiv · Nov 14, 2022Biochemistry

The in situ structure of Parkinson’s disease-linked LRRK2

R. Watanabe, R. Buschauer, J. Boehning, M. Audagnotto, K. Lasker, T. W. Lu, D. Boassa, S. Taylor, E. Villa

This study uses cryo-electron tomography to reveal the in situ structure of LRRK2 with a pathogenic mutation, showing its oligomerization around microtubules and functional domains.

bioRxiv · Nov 10, 2019Biophysics

Molecular mechanism of translational stalling by inhibitory codon combinations and poly(A) tracts

P. Tesina, L. N. Lessen, R. Buschauer, J. Cheng, C. C.-C. Wu, O. Berninghausen, A. R. Buskirk, T. Becker, R. Beckmann, R. Green

This study identifies molecular mechanisms of translational stalling caused by inhibitory codon pairs and poly(A) tracts using in vitro biochemistry, ribosome profiling, and cryo-EM.

bioRxiv · Sep 4, 2019Biochemistry