Thermodynamic Analysis of Protein-Nanoparticle Interactions Links Binding Affinity and Structural Stability
When nanoparticles and nanoplastics enter biological fluids, their surfaces are rapidly coated with proteins, forming a corona that governs biological responses. However, understanding protein- surface interaction energetics remains a significant challenge. Here, we examine how protein charge distribution affects adsorption to polystyrene nanoparticles (PSNPs) by generating a series of lysine-to-alanine variants of the GB3 protein. Using isothermal titration calorimetry (ITC), we found that the K19A variant binds most strongly to both non-functionalized and carboxylate- functionalized PSNPs. ITC thermograms indicate that K19A forms a stable monolayer, while other variants exhibit multilayer adsorption. We hypothesize that removing lysine at position 19 creates a flatter, more neutral interaction surface that promotes efficient initial binding. Fluorescence denaturation experiments show that PSNPs destabilize GB3 protein variants, and binding correlates strongly with protein unfolding (r = 0.82, p < 0.01 for COOH-PSNPs and r = 0.76, p < 0.03 for non-functionalized PSNPs). These results reveal how protein stability and charge distribution shape adsorption thermodynamics, offering a framework for predicting protein-surface interactions. TOC Image O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=134 SRC="FIGDIR/small/671591v1_ufig1.gif" ALT="Figure 1"> View larger version (31K): org.highwire.dtl.DTLVardef@1741baforg.highwire.dtl.DTLVardef@1c5be81org.highwire.dtl.DTLVardef@15e3118org.highwire.dtl.DTLVardef@e92583_HPS_FORMAT_FIGEXP M_FIG C_FIG