Supported lysozyme for improved antimicrobial surface protection

J Colloid Interface Sci. 2021 Jan 15;582(Pt B):764-772. doi: 10.1016/j.jcis.2020.08.107. Epub 2020 Aug 29.

Abstract

Surface protection against biofilms is still an open challenge. Current strategies rely on coatings that are meant to guarantee antiadhesive or antimicrobial effects. While it seems difficult to ensure antiadhesion in complex media and against all the adhesive arsenal of microbes, strategies based on antimicrobials lack from sustainable functionalization methodologies to allow the perfect efficiency of the grafted molecules. Here we used the high affinity ligand-receptor interaction between biotin and streptavidin to functionalize surfaces with lysozyme, an enzyme that degrades the bacterial peptidoglycan cell wall. Biotinylated lysozyme was grafted on surfaces coated with streptavidin receptors. Using atomic force microscopy (AFM)-based single molecule force spectroscopy, we showed that grafting through ligand-receptor interaction allows the correct orientation of the enzyme on the substrate for enhanced activity towards the microbial target. The antibacterial efficiency was tested against Micrococcus luteus and revealed that surface protection was improved when lysozyme was grafted through the ligand-receptor interaction. These results suggest that bio-molecular interactions are promising for a sustainable grafting of antimicrobial agents on surfaces.

Keywords: Antimicrobial surfaces; Ligand-receptor grafting; Lysozyme; Micrococcus luteus; Single-molecule force spectroscopy.

MeSH terms

  • Anti-Bacterial Agents / pharmacology
  • Anti-Infective Agents* / pharmacology
  • Microscopy, Atomic Force
  • Muramidase*
  • Streptavidin
  • Surface Properties

Substances

  • Anti-Bacterial Agents
  • Anti-Infective Agents
  • Streptavidin
  • Muramidase