Versatile Supramolecular Complex for Targeted Antimicrobial Photodynamic Inactivation
Author
Other authors
Publication date
2022-04-20ISSN
1520-4812
Abstract
We report the development of a supramolecular structure endowed with photosensitizing properties and targeting capability for antimicrobial photodynamic inactivation. Our synthetic strategy uses the tetrameric bacterial protein streptavidin, labeled with the photosensitizer eosin, as the main building block. Biotinylated immunoglobulin G (IgG) from human serum, known to associate with Staphylococcus aureus protein A, was bound to the complex streptavidin–eosin. Fluorescence correlation spectroscopy and fluorescence microscopy demonstrate binding of the complex to S. aureus. Efficient photoinactivation is observed for S. aureus suspensions treated with IgG–streptavidin–eosin at concentrations higher than 0.5 μM and exposed to green light. The proposed strategy offers a flexible platform for targeting a variety of molecules and microbial species.
Document Type
Article
Document version
Published version
Language
English
Subject (CDU)
577 - Material bases of life. Biochemistry. Molecular biology. Biophysics
579 - Microbiology
612 - Physiology. Human and comparative physiology
Keywords
Bacteria
Conjugate Acid-Base Pairs
Fluorescence
Monomers
Peptides and proteins
Fluorescència
Monòmers
Pèptids
Proteïnes
Bacteris
Pages
p.11
Publisher
American Chemical Society
Is part of
Bioconjugate Chemistry 2022, 33(4), 666–676
This item appears in the following Collection(s)
Rights
© L'autor/a
Except where otherwise noted, this item's license is described as http://creativecommons.org/licenses/by/4.0/