Author

Mona Johannessen

UiT The Arctic University of NorwayORCID 0000-0003-4604-8600Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Microbiology· 2 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Assay:proteomics· 2 Organism:bacteria (other)· 1 Research Focus:cell type annotation· 1 Research Focus:gene regulatory network inference· 1 Approach:genetic perturbation / CRISPR· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

Christian Stephan LentziD· 3 shared Frerich M. MassoniD· 1 shared George RandalliD· 1 shared Jiyun ZhuiD· 1 shared Kristin HegstadiD· 1 shared Laura van EijkiD· 1 shared Marcel R. de ZoeteiD· 1 shared Marco C. Viveen· 1 shared

Activity by Year

2024-2024 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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3 shared papersMicrobiology

Christian Stephan LentzORCID

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3 papers

Recent·Most cited

MicrobiologybioRxivPreprintNov 27, 2024

A programmable, selection-free CRISPR interference system in Staphylococcus aureus

Roni Miah, Mona Johannessen, Morten Kjos, Christian Stephan Lentz

This paper develops a selection-free CRISPRi system in S. aureus that silences virulence genes without antibiotic selection or exogenous inducers, validated in vitro and in vivo.

DOI 10.1101/2024.11.27.625599

bacteria (other)genetic perturbation / CRISPR

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MicrobiologybioRxivPreprintMay 28, 2024

Activity-Based Protein Profiling Identifies Klebsiella pneumoniae Serine Hydrolases with Potential Roles in Host-Pathogen Interactions

Md Jalal Uddin, George Randall, Jiyun Zhu…·Christian Stephan Lentz

2 citations

humanproteomics

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Molecular BiologymSystemsPeer-reviewedApr 24, 2024

Deciphering Staphylococcus aureus-host dynamics using dual activity-based protein profiling of ATP-interacting proteins

Stephen Dela Ahator, Kristin Hegstad, Christian Stephan Lentz, Mona Johannessen

This study uses ATP-interacting protein profiling to analyze S. aureus-host interactions in macrophages and keratinocytes, revealing cell-type specific adaptations and metabolic shifts.

3 citations

humanproteomics

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