Author

R. J. Braun

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· 1 Biophysics· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 3 Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Research Focus:protein folding & dynamics· 2 Assay:proteomics· 2 Organism:yeast· 2 Organism:human· 1 Assay:protein structure· 1

Frequent Co-Authors

A. Brudnicka· 1 shared A. M. Schlagowski· 1 shared A. Sachez Vicente· 1 shared B. Westermann· 1 shared E. Reynolds· 1 shared F. Boos· 1 shared F. Stein· 1 shared G. Charvin· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

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1 shared paperCell Biology

A. Brudnicka

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Tld1 is a novel regulator of triglyceride lipolysis that demarcates a lipid droplet subpopulation

N. O. Speer, R. J. Braun, E. Reynolds, A. Brudnicka, J. Swanson, W. M. Henne

The paper identifies Tld1 as a regulator of triglyceride lipolysis that specifically targets TG-rich lipid droplets and modulates lipolysis in yeast.

bioRxiv · Mar 7, 2023Cell Biology

Capturing the liquid-crystalline phase transformation: Implications for protein targeting to sterol ester-rich lipid droplets

R. J. Braun, J. M. Swanson

The paper studies how an increase in sterol ester concentration induces a liquid-crystalline phase transformation in lipid droplets, altering their physical properties and affecting protein association.

bioRxiv · Jun 5, 2022Biophysics

Increased levels of the mitochondrial import factor Mia40 prevent the aggregation of polyQ proteins in the cytosol

A. M. Schlagowski, K. Knöringer, S. Morlot, A. Sachez Vicente, F. Boos, N. Khalid, S. Ahmed, J. Schramm, L. M. Murschall, P. Haberkant, F. Stein, J. Riemer, B. Westermann, R. J. Braun, K. F. Winklhofer, , J. M. Herrmann

The paper shows that overexpressing Mia40 reduces toxic polyQ protein aggregates in yeast and human cells by competing for chaperone and proteasome resources.

bioRxiv · Feb 2, 2021Biochemistry