Probing IgG1 FC-Multimodal Nanoparticle Interactions: A Combined Nuclear Magnetic Resonance and Molecular Dynamics Simulations Approach

In this study, NMR and molecular dynamics simulations were employed to study IgG1 F-C binding to multimodal surfaces. Gold nanoparticles functionalized with two multimodal cation-exchange ligands (Capto and Nuvia) were synthesized and employed to carry out solution-phase NMR experiments with the F-C. Experiments with perdeuterated N-15-labeled F-C and the multimodal surfaces revealed micromolar residue-level binding affinities as compared to millimolar binding affinities with these ligands in free solution, likely due to cooperativity and avidity effects. The binding of F-C with the Capto ligand nanoparticles was concentrated near an aliphatic cluster in the C(H)2/C(H)3 interface, which corresponded to a focused hydrophobic region. In contrast, binding with the Nuvia ligand nanoparticles was more diffuse and corresponded to a large contiguous positive electrostatic potential region on the side face of the F-C. Results with lower-ligand-density nanoparticles indicated a decrease in binding affinity for both systems. For the Capto ligand system, several aliphatic residues on the F-C that were important for binding to the higher-density surface did not interact with the lower-density nanoparticles. In contrast, no significant difference was observed in the interacting residues on the F-C to the high- and low-ligand density Nuvia surfaces. The binding affinities of F-C to both multimodal-functionalized nanoparticles decreased in the presence of salt due to the screening of multiple weak interactions of polar and positively charged residues. For the Capto ligand nanoparticle system, this resulted in an even more focused hydrophobic binding region in the interface of the C(H)2 and C(H)3 domains. Interestingly, for the Nuvia ligand nanoparticles, the presence of salt resulted in a large transition from a diffuse binding region to the same focused binding region determined for Capto nanoparticles at 150 mM salt. Molecular dynamics simulations corroborated the NMR results and provided important insights into the molecular basis of F-C binding to these different multimodal systems containing clustered (observed at high-ligand densities) and nonclustered ligand surfaces. This combined biophysical and simulation approach provided significant insights into the interactions of F-C with multimodal surfaces and sets the stage for future analyses with even more complex biotherapeutics.

Automated summary

This study utilized NMR and molecular dynamics simulations to investigate the binding of IgG1 F-C to multimodal surfaces, showing significantly increased binding affinities on the multimodal surfaces. Different ligands exhibited distinct binding modes and regions with F-C, which were influenced by the presence of salt. Molecular dynamics simulations confirmed the experimental findings and provided insights into the molecular basis of binding between F-C and clustered/nonclustered ligand surfaces in multimodal systems.