Author

L. M. Nolan

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· 6

Signature Assays, Organisms & Methods

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Approach:experimental assay· 5 Organism:bacteria (other)· 4 Research Focus:cell signaling & trafficking· 3 Research Focus:cell type annotation· 3 Research Focus:host-pathogen & immune response· 3 Assay:proteomics· 2 Research Focus:development & morphogenesis· 1 Research Focus:drug response / drug discovery· 1

Frequent Co-Authors

C. B. Whitchurch· 4 shared L. Turnbull· 3 shared J. J. Lazenby· 2 shared L. C. McCaughey· 2 shared A. A. Sabnis· 1 shared A. Filloux· 1 shared A. K. Cain· 1 shared A. L. Hynen· 1 shared

Activity by Year

2019-2023 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 14 mutual co-author links

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4 shared papersMicrobiology

C. B. Whitchurch

Mutual co-authors in cluster

Author profile →

6 papers

Recent·Most cited

Antimicrobial peptide glatiramer acetate targets Pseudomonas aeruginosa lipopolysaccharides to breach membranes without altering lipopolysaccharide modification

R. A. Murphy, J. Pizzato, L. Cuthbertson, A. A. Sabnis, A. M. Edwards, L. M. Nolan, T. Vorup-Jensen, G. Larrouy-Maumus, J. C. Davies

This study shows glatiramer acetate binds and neutralizes Pseudomonas aeruginosa lipopolysaccharides and extracellular DNA, enhancing antibiotic efficacy without inducing resistance mechanisms.

bioRxiv · May 23, 2023 · PreprintMicrobiology

Bacteriophage infection produces membrane vesicles in Escherichia coli via both explosive cell lysis and membrane blebbing

P. K. Mandal, G. B. Ballerin, L. M. Nolan, N. K. Petty, C. B. Whitchurch

bioRxiv · Dec 23, 2020Microbiology

Multiple Holins Contribute to Extracellular DNA Release in Pseudomonas aeruginosa Biofilms

A. L. Hynen, J. J. Lazenby, G. M. Savva, L. C. McCaughey, L. Turnbull, L. M. Nolan, C. B. Whitchurch

This study identifies three holins involved in eDNA release during Pseudomonas aeruginosa biofilm development, showing their role in microcolony formation and eDNA release dynamics.

bioRxiv · Oct 28, 2020Microbiology

Pseudomonas aeruginosa is capable of natural transformation in biofilms

L. M. Nolan, L. Turnbull, M. Katrib, S. R. Osvath, D. Losa, J. J. Lazenby, C. B. Whitchurch

This study shows Pseudomonas aeruginosa in biofilms can undergo natural transformation, challenging previous assumptions about its capability.

bioRxiv · Apr 6, 2020Microbiology

ChpC controls twitching motility-mediated expansion of Pseudomonas aeruginosa biofilms in response to serum albumin, mucin and oligopeptides

L. M. Nolan, L. C. McCaughey, J. Merjane, L. Turnbull, C. B. Whitchurch

This study shows ChpC is required for Pseudomonas aeruginosa twitching motility response to serum albumin, mucin, and oligopeptides, while cAMP and T4P levels are independent of ChpC.

bioRxiv · Oct 31, 2019Microbiology

Discovery of a Pseudomonas aeruginosa Type VI secretion system toxin targeting bacterial protein synthesis using a global genomics approach

L. M. Nolan, A. K. Cain, E. Manoli, M. A. Sainz-Polo, G. Dougan, D. A. I. Mavridou, D. Albesa-Jove, J. Parkhill, A. Filloux

The paper uses TraDIS to identify T6SS toxins in Pseudomonas aeruginosa, finding Tse8 targets bacterial protein synthesis by disrupting the transamidosome complex.

bioRxiv · Aug 13, 2019 · PreprintMicrobiology