Author

J. Riemer

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· 3

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 3 Approach:experimental assay· 3 Organism:human· 3 Research Focus:cell type annotation· 2 Assay:proteomics· 2 Organism:yeast· 2 Research Focus:chromatin & epigenetic regulation· 1 Assay:imaging· 1

Frequent Co-Authors

B. Morgan· 2 shared L. M. Murschall· 2 shared A. Diederich· 1 shared A. M. Schlagowski· 1 shared A. Sachez Vicente· 1 shared B. Westermann· 1 shared C. Bell· 1 shared C. Grashoff· 1 shared

Activity by Year

2021-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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2 shared papersBiochemistry

B. Morgan

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

The NAPstar family of NADP redox state sensors highlights glutathione as the primary mediator of anti-oxidative electron flux

M. Scherschel, J.-O. Niemeier, L. Jacobs, M. Hoffmann, A. Diederich, C. Bell, P. Hoehne, S. Raetz, J. Kroll, J. Steinbeck, S. Lichtenauer, J. Multhoff, J. Zimmermann, T. Sadhanasatish, R. A. Rothemann, , B. Morgan

The paper introduces NAPstar biosensors to measure NADP redox states and finds glutathione mediates anti-oxidative electron flux across eukaryotes.

bioRxiv · Feb 14, 2024 · PreprintBiochemistry

Thioredoxin reductase controls the capacity of peroxiredoxins to limit mitochondrial H2O2 release

M. N. Hoehne, L. J. Jacobs, K. J. Lapacz, L. M. Murschall, T. Marker, B. Morgan, M. Fricker, V. Belousov, J. Riemer

The paper investigates mitochondrial H2O2 release in mammalian cells and finds that peroxiredoxins 1 and 2 control H2O2 gradients and handling through dynamic adaptation of thioredoxin reductase.

bioRxiv · Jul 8, 2021 · PreprintBiochemistry

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