A generic approach based on long-lifetime fluorophores for the assessment of protein binding to polymer nanoparticles by fluorescence anisotropy

• Published in: Nanoscale Vol. 16; no. 7; pp. 3659 - 3667
• Main Authors: Ahmed, Marwa A, Hessz, Dóra, Gyarmati, Benjámin, Páncsics, Mirkó, Kovács, Norbert, Gyurcsányi, Róbert E, Kubinyi, Miklós, Horváth, Viola
• Format: Journal Article
• Language: English
• Published: England Royal Society of Chemistry 15.02.2024
• Subjects: Acrylic acid; Anisotropy; Binding; Chemical compounds; Fluorescence; Fluorescence Polarization; Fluorescent Dyes; In vitro methods and tests; In vivo methods and tests; Isopropylacrylamide; Lysozyme; Nanoparticles; Polymers; Protein Binding; Proteins; Reagents
• ISSN: 2040-3364; 2040-3372
• DOI: 10.1039/d3nr02460a

Quantitation of protein-nanoparticle interactions is essential for the investigation of the protein corona around NPs in vivo and when using synthetic polymer nanoparticles as affinity reagents for selective protein recognition in vitro . Here, a method based on steady-state fluorescence anisotropy measurement is presented as a novel, separation-free tool for the assessment of protein-nanoparticle interactions. For this purpose, a long-lifetime luminescent Ru-complex is used for protein labelling, which exhibits low anisotropy when conjugated to the protein but displays high anisotropy when the proteins are bound to the much larger polymer nanoparticles. As a proof of concept, the interaction of lysozyme with poly( N -isopropylacrylamide- co-N-tert -butylacrylamide- co -acrylic acid) nanoparticles is studied, and fluorescence anisotropy measurements are used to establish the binding kinetics, binding isotherm and a competitive binding assay. Using long-lifetime fluorophores as protein labels, protein-nanoparticle interactions can be monitored through anisotropy change. Besides gaining thermodynamic and kinetic information on the binding process, competitive protein assays can be set up.