Versatile Supramolecular Complex for Targeted Antimicrobial Photodynamic Inactivation
Autor/a
Mussini, Andrea
Uriati, Eleonora
Hally, Cormac
Nonell, Santi
Bianchini, Paolo
Diaspro, Alberto
Pongolini, Stefano
Delcanale, Pietro
Abbruzzetti, Stefania
Viappiani, Cristiano
Otros/as autores/as
Universitat Ramon Llull. IQS
Fecha de publicación
2022-04-20ISSN
1520-4812
Resumen
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.
Tipo de documento
Artículo
Versión del documento
Versión publicada
Lengua
English
Materias (CDU)
577 - Bioquímica. Biología molecular. Biofísica
579 - Microbiología
612 - Fisiología
Palabras clave
Bacteria
Conjugate Acid-Base Pairs
Fluorescence
Monomers
Peptides and proteins
Fluorescència
Monòmers
Pèptids
Proteïnes
Bacteris
Páginas
p.11
Publicado por
American Chemical Society
Publicado en
Bioconjugate Chemistry 2022, 33(4), 666–676
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