Author

S. Vanmarcke

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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Microbiology· 2 Bioengineering· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:drug response / drug discovery· 2 Assay:protein sequence· 2 Research Focus:cell type annotation· 1 Organism:human· 1 Organism:yeast· 1

Frequent Co-Authors

N. Callewaert· 3 shared L. van Schie· 2 shared S. Devos· 2 shared W. Nerinckx· 2 shared A. Madder· 1 shared A. Van Hecke· 1 shared A.-S. De Smet· 1 shared B. Laukens· 1 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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3 shared papersMicrobiology

N. Callewaert

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Yeast-based production platform for potent and stable heavy chain-only antibodies

C. Lonigro, H. Eeckhaut, R. A. Symakani, K. Roose, B. Schepens, K. Sedeyn, A.-S. De Smet, J. C. Zavala Marchan, P. Vanhaverbeke, S. Vanmarcke, K. Claes, S. De Cae, H. Demol, S. Devos, D. Fijalkowska, , N. Callewaert

This paper presents a yeast-based platform for producing stable and potent heavy chain-only antibodies, demonstrating its effectiveness with an anti-SARS-CoV-2 example.

bioRxiv · Mar 4, 2024 · PreprintMicrobiology

GlyConnect: a glycan-based conjugation extension of the GlycoDelete technology

W. Van Breedam, K. Thooft, F. Santens, S. Vanmarcke, E. Wyseure, B. Laukens, B. Van Moer, W. Nerinckx, S. Devos, A. Madder, N. Callewaert

The paper evaluates and optimizes chemical and chemo-enzymatic conjugation methods for GlycoDelete-type glycans on benchmark proteins.

bioRxiv · Jun 2, 2021 · PreprintBioengineering

Use of a counterselectable transposon to create markerless knockouts from a 18,432-clone ordered M. bovis BCG mutant resource

K. Borgers, K. Vandewalle, A. Van Hecke, G. Michielsen, E. Plets, L. van Schie, S. Vanmarcke, L. Schindfessel, N. Festjens, N. Callewaert

The paper describes a method to generate markerless knockouts from a large transposon mutant library in M. bovis BCG, creating an ordered mutant resource targeting 83% of non-essential genes.

bioRxiv · Oct 24, 2019 · PreprintMicrobiology