Exploiting the Fc base of IgG antibodies to create functional nanoparticle conjugates
Al Qaraghuli, Mohammed M. and Kubiak-Ossowska, Karina and Ferro, Valerie A. and Mulheran, Paul A. (2024) Exploiting the Fc base of IgG antibodies to create functional nanoparticle conjugates. Scientific Reports, 14 (1). 14832. ISSN 2045-2322 (https://doi.org/10.1038/s41598-024-65822-7)
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Abstract
The structures of the Fc base of various IgG antibodies have been examined with a view to understanding how this region can be used to conjugate IgG to nanoparticles. The base structure is found to be largely consistent across a range of species and subtypes, comprising a hydrophobic region surrounded by hydrophilic residues, some of which are charged at physiological conditions. In addition, atomistic Molecular Dynamics simulations were performed to explore how model nanoparticles interact with the base using neutral and negatively charged gold nanoparticles. Both types of nanoparticle interacted readily with the base, leading to an adaptation of the antibody base surface to enhance the interactions. Furthermore, these interactions left the rest of the domain at the base of the Fc region structurally intact. This implies that coupling nanoparticles to the base of an IgG molecule is both feasible and desirable, since it leaves the antibody free to interact with its surroundings so that antigen-binding functionality can be retained. These results will therefore help guide future attempts to develop new nanotechnologies that exploit the unique properties of both antibodies and nanoparticles.
ORCID iDs
Al Qaraghuli, Mohammed M. ORCID: https://orcid.org/0000-0003-1823-6671, Kubiak-Ossowska, Karina, Ferro, Valerie A. ORCID: https://orcid.org/0000-0003-1967-3603 and Mulheran, Paul A. ORCID: https://orcid.org/0000-0002-9469-8010;-
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Item type: Article ID code: 89841 Dates: DateEvent27 June 2024Published27 June 2024Published Online25 June 2024AcceptedOctober 2023SubmittedSubjects: Science > Physics > Atomic physics. Constitution and properties of matter Department: Faculty of Engineering > Chemical and Process Engineering
Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical SciencesDepositing user: Pure Administrator Date deposited: 05 Jul 2024 09:34 Last modified: 16 Dec 2024 02:46 URI: https://strathprints.strath.ac.uk/id/eprint/89841