Author

A. Matouschek

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 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:cell type annotation· 1 Assay:ChIP-seq· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1

Frequent Co-Authors

B. L. Spaller· 1 shared C. Davis· 1 shared D. Corujo· 1 shared D. Finley· 1 shared E. Choi· 1 shared F. Gong· 1 shared F. Medina· 1 shared H. Chong· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperBiochemistry

B. L. Spaller

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Author profile →

2 papers

Recent·Most cited

A strict requirement in proteasome substrates for spacing between ubiquitin tag and degradation initiation elements

C. Davis, B. L. Spaller, E. Choi, J. B. Kurrasch, H. Chong, S. Elsasser, D. Finley, A. Matouschek

The paper shows that the distance between ubiquitin tags and degradation initiation elements determines proteasome-mediated protein degradation efficiency.

bioRxiv · Aug 8, 2023 · PreprintBiochemistry

Poly(ADP-ribose)-binding and macroH2A mediate recruitment and functions of KDM5A at DNA lesions

R. R. Kumbhar, J. Perren, F. Gong, D. Corujo, F. Medina, A. Matouschek, M. Buschbeck, K. M. Miller

This study identifies PAR-binding and macroH2A1.2 as factors that mediate KDM5A recruitment to DNA damage sites, enhancing its repair and transcriptional functions at chromatin breaks.

bioRxiv · Jul 27, 2020Cell Biology