Author

N. Landscheidt

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· 2

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 2 Research Focus:chromatin & epigenetic regulation· 2 Approach:experimental assay· 2 Research Focus:protein folding & dynamics· 1 Assay:protein sequence· 1 Assay:protein structure· 1 Assay:proteomics· 1

Frequent Co-Authors

J. D. Knopf· 2 shared M. K. Lemberg· 2 shared N. Kuehnle· 2 shared B. L. Schulz· 1 shared C. L. Pegg· 1 shared C.-W. Chao· 1 shared J. Bock· 1 shared J.-G. Lee· 1 shared

Activity by Year

2020-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersCell Biology

J. D. Knopf

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2 papers

Recent·Most cited

Rhomboid protease RHBDL4 promotes retrotranslocation of aggregation-prone proteins for degradation

J. Bock, N. Kuehnle, J. D. Knopf, N. Landscheidt, J.-G. Lee, Y. Ye, M. K. Lemberg

This study identifies RHBDL4 as a rhomboid protease that promotes retrotranslocation of aggregation-prone proteins for degradation, working with the erlin ERAD complex.

bioRxiv · Dec 17, 2021Cell Biology

Intramembrane protease RHBDL4 cleaves oligosaccharyltransferase subunits to target them for ER-associated degradation

J. D. Knopf, N. Landscheidt, C. L. Pegg, B. L. Schulz, N. Kuehnle, C.-W. Chao, S. Huck, M. K. Lemberg

This study identifies RHBDL4 as a regulator of the oligosaccharyltransferase complex through ERAD-mediated degradation, revealing a novel link between ERAD and glycosylation regulation.

bioRxiv · Jan 19, 2020Cell Biology