Rebecca V Vince
Identification of methicillin-resistant Staphylococcus aureus-specific peptides for targeted photoantimicrobial chemotherapy
Vince, Rebecca V; Madden, Leigh A; Alonso, Cristina M. A.; Boyle, Ross W; Vince, Rebecca V.; Madden, Leigh A.; Vince, Rebecca; Alonso, Cristina M.A.; Savoie, Huguette; Boyle, Ross W.; Todman, Martin; Paget, Tim; Greenman, John
Authors
Leigh A Madden
Cristina M. A. Alonso
Ross W Boyle
Rebecca V. Vince
Leigh A. Madden
Dr Rebecca Vince Rebecca.Vince@hull.ac.uk
Senior Lecturer in Health Physiology
Cristina M.A. Alonso
Huguette Savoie
Professor Ross Boyle R.W.Boyle@hull.ac.uk
Professor of Biological Chemistry
Martin Todman
Tim Paget
Professor John Greenman J.Greenman@hull.ac.uk
Professor of Tumour Immunology
Abstract
The increasing prevalence of multi-drug resistant bacteria, such as methicillin-resistant Staphylococcus aureus (MRSA), necessitates development of alternative modes of bacterial targeting which are not hindered by antibiotic resistance and minimise collateral damage. To achieve this, the FliTrx (TM) bacterially-displayed peptide library was panned against MRSA and randomly selected clones (n = 20) were DNA sequenced. One selected peptide was synthesised as both cyclic and linear constructs. Binding of the cyclic construct was observed by flow cytometry against isolates of MRSA whilst the linear construct showed low affinity. Low reactivity was observed with other Staphylococcal sp., Gram-negative bacteria and human keratinocytes. The selected peptide was also cloned in-frame, within the thioredoxin gene into the pPROTet. E 6xHN vector for protein expression. A porphyrin photosensitiser (5-(4-isothiocyanatophenyl)-10,15,20-tris(4-N-methylpyridiniumyl) porphyrin trichloride) was conjugated to the recombinant protein and the in vitro cytotoxic effect of the resulting bioconjugate was determined against MRSA and other non-specific bacterial and mammalian cell lines. Photoantimicrobial chemotherapy (PACT) using the bioconjugate showed a 66% reduction in MRSA growth in comparison with non-irradiated cells. This work demonstrates the potential to isolate peptides with binding specificity against MRSA that can be used for targeted PACT, providing an effective alternative to antibody targeting.
Citation
Vince, R. V., Madden, L. A., Alonso, C. M., Savoie, H., Boyle, R. W., Todman, M., Paget, T., & Greenman, J. (2011). Identification of methicillin-resistant Staphylococcus aureus-specific peptides for targeted photoantimicrobial chemotherapy. Photochemical & photobiological sciences : an international journal, 10(4), 515-522. https://doi.org/10.1039/c0pp00267d
Journal Article Type | Article |
---|---|
Acceptance Date | Nov 8, 2010 |
Publication Date | Apr 1, 2011 |
Journal | PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES |
Print ISSN | 1474-905X |
Publisher | Royal Society of Chemistry |
Peer Reviewed | Peer Reviewed |
Volume | 10 |
Issue | 4 |
Pages | 515-522 |
DOI | https://doi.org/10.1039/c0pp00267d |
Keywords | antimicrobial photodynamic therapy lethal photosensitization in-vitro antibiotic-resistance cyclic peptide porphyrin library binding system inactivation |
Public URL | https://hull-repository.worktribe.com/output/400120 |
Publisher URL | http://pubs.rsc.org/en/Content/ArticleLanding/2011/PP/C0PP00267D#!divAbstract |
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