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Preventing E. coli Biofilm Formation with Antimicrobial Peptide-Functionalized Surface Coatings: Recognizing the Dependence on the Bacterial Binding Mode Using Live-Cell Microscopy

Hansson, Adam, 1993 (author)
RISE,Gothenburg University,Göteborgs universitet,Institutionen för kemi och molekylärbiologi,Department of Chemistry and Molecular Biology,Metodik för produktframtagning,University of Gothenburg, Sweden
Karlsen, Eskil Andre (author)
UiT The Arctic University of Norway, Norway; Amicoat A/S, Norway
Stensen, Wenche (author)
UiT The Arctic University of Norway, Norway
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Svendsen, John S. M. (author)
UiT The Arctic University of Norway, Norway; Amicoat A/S, Norway
Berglin, Mattias, 1970 (author)
RISE,Gothenburg University,Göteborgs universitet,Institutionen för kemi och molekylärbiologi,Department of Chemistry and Molecular Biology,Metodik för produktframtagning,University of Gothenburg, Sweden
Lundgren, Anders, 1978 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kemi och molekylärbiologi,CARe - Centrum för antibiotikaresistensforskning,Department of Chemistry and Molecular Biology,Centre for antibiotic resistance research, CARe,University of Gothenburg, Sweden
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 (creator_code:org_t)
American Chemical Society, 2024
2024
English.
In: ACS APPLIED MATERIALS & INTERFACES. - : American Chemical Society. - 1944-8244 .- 1944-8252. ; 16:6, s. 6799-6812
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Antimicrobial peptides (AMPs) can kill bacteria by destabilizing their membranes, yet translating these molecules' properties into a covalently attached antibacterial coating is challenging. Rational design efforts are obstructed by the fact that standard microbiology methods are ill-designed for the evaluation of coatings, disclosing few details about why grafted AMPs function or do not function. It is particularly difficult to distinguish the influence of the AMP's molecular structure from other factors controlling the total exposure, including which type of bonds are formed between bacteria and the coating and how persistent these contacts are. Here, we combine label-free live-cell microscopy, microfluidics, and automated image analysis to study the response of surface-bound Escherichia coli challenged by the same small AMP either in solution or grafted to the surface through click chemistry. Initially after binding, the grafted AMPs inhibited bacterial growth more efficiently than did AMPs in solution. Yet, after 1 h, E. coli on the coated surfaces increased their expression of type-1 fimbriae, leading to a change in their binding mode, which diminished the coating's impact. The wealth of information obtained from continuously monitoring the growth, shape, and movements of single bacterial cells allowed us to elucidate and quantify the different factors determining the antibacterial efficacy of the grafted AMPs. We expect this approach to aid the design of elaborate antibacterial material coatings working by specific and selective actions, not limited to contact-killing. This technology is needed to support health care and food production in the postantibiotic era.

Subject headings

TEKNIK OCH TEKNOLOGIER  -- Nanoteknik (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Nano-technology (hsv//eng)
TEKNIK OCH TEKNOLOGIER  -- Medicinteknik (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Medical Engineering (hsv//eng)

Keyword

antimicrobial peptides
antibiotics resistance
biofilms
fimbriae
surface coatings
live-cell microscopy
microfluidics
image analysis
Anti-Bacterial Agents; Antimicrobial Peptides; Bacteria; Biofilms; Coated Materials

Publication and Content Type

ref (subject category)
art (subject category)

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