Author

K. M. Bonger

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 Immunology· 1

Signature Assays, Organisms & Methods

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Assay:proteomics· 3 Research Focus:cell type annotation· 2 Research Focus:drug response / drug discovery· 2 Approach:experimental assay· 2 Organism:human· 2 Organism:mouse· 2 Research Focus:protein folding & dynamics· 2 Organism:bacteria (other)· 1

Frequent Co-Authors

B. J. Ignacio· 2 shared A. Cammarata· 1 shared B. Naus· 1 shared C. G. Figdor· 1 shared C. M. Le Gall· 1 shared D. van Dalen· 1 shared E. Slot· 1 shared E. Storkebaum· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersImmunology

B. J. Ignacio

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Author profile →

3 papers

Recent·Most cited

In-depth immunometabolic profiling by measuring cellular protein translation inhibition via bioorthogonal noncanonical amino acid tagging (CENCAT)

F. Vrieling, H. J. P. van der Zande, B. Naus, L. Smeehuijzen, B. J. Ignacio, K. M. Bonger, J. van den Bossche, S. Kersten, R. Stienstra

The paper introduces CENCAT, a method to measure protein synthesis inhibition in immune cells using noncanonical amino acid tagging, showing its utility in analyzing metabolic responses in complex samples and tissue-resident immune cells.

bioRxiv · Aug 3, 2023 · PreprintImmunology

THRONCAT: Efficient metabolic labeling of newly synthesized proteins using a bioorthogonal threonine analog

B. J. Ignacio, J. Dijkstra, N. MoraGarcia, E. Slot, M. van Weijsten, E. Storkebaum, M. Vermeulen, K. M. Bonger

THRONCAT enables efficient, non-toxic labeling of newly synthesized proteins in various organisms using a threonine analog, demonstrating its utility in studying proteome dynamics and disease models.

bioRxiv · Mar 29, 2022Cell Biology

Dual site-specific chemoenzymatic antibody fragment conjugation using CRISPR-based hybridoma engineering

C. M. Le Gall, J. M. van der Schoot, I. Ramos-Tomillero, M. Parlak Khalily, F. J. van Dalen, Z. Wijfjes, L. Smeding, D. van Dalen, A. Cammarata, K. M. Bonger, C. G. Figdor, F. A. Scheeren, M. Verdoes

This paper introduces a CRISPR-based method to engineer hybridoma cells that secrete dual-tagged Fab fragments, enabling site-specific conjugation of multiple cargos.

bioRxiv · Dec 8, 2020Biochemistry