Author

J. W. Bode

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Biochemistry· 1 Cell Biology· 1 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 3 Organism:human· 3 Assay:proteomics· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Approach:deep learning· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1

Frequent Co-Authors

J. E. Corn· 2 shared J. Farnung· 2 shared M. Muhar· 2 shared R. M. Benoit· 2 shared C. Mueller· 1 shared C. Vaccarin· 1 shared D. Beyer· 1 shared J. R. Liang· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersCell Biology

J. E. Corn

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Development of radiofluorinated MLN-4760 derivatives for PET imaging of the SARS-CoV-2 entry receptor ACE2

J. Wang, D. Beyer, C. Vaccarin, Y. He, M. Tanriver, R. M. Benoit, X. Deupi, L. Mu, J. W. Bode, r. Schibli, C. Mueller

This paper develops and evaluates radiofluorinated derivatives of MLN-4760 for PET imaging of ACE2, finding that [18F]F-MLN-4760 shows superior binding affinity and yield.

bioRxiv · Mar 20, 2024Pharmacology & Toxicology

C-terminal amides mark proteins for degradation via SCF/FBXO31

M. Muhar, J. Farnung, R. Hofmann, M. Cernakova, N. D. Sidiropoulos, J. W. Bode, J. E. Corn

The paper identifies C-terminal amides as signals for protein degradation via SCF/FBXO31, showing that oxidative stress generates these marks and a mutation disrupts this process, leading to toxicity.

bioRxiv · Jun 29, 2023Cell Biology

Human ATG3 contains a non-canonical LIR motif crucial for its enzymatic activity in autophagy

J. Farnung, M. Muhar, J. R. Liang, K. A. Tolmachova, R. M. Benoit, J. E. Corn, J. W. Bode

The paper identifies a non-canonical LIR motif in ATG3 essential for its enzymatic activity in autophagy, showing its role in LC3 lipidation and thioester formation.

bioRxiv · Aug 2, 2022 · PreprintBiochemistry