Search

The composition, orientation, and conformation of proteins in biomolecular coronas acquired by nanoparticles in biological media contribute to how they are identified by a cell. While numerous stud...

The interaction of lipopolysaccharides (LPS) with metal cations strongly affects the stability and function of the Gram-negative bacterial outer membrane. The sensitivity of deep rough (Re) LPS packing and function to the ionic environment, as affected by cation valency and ionic radius, has been determined using molecular dynamics simulations and Langmuir balance experiments. The degree of LPS aggregation within the LPS models in the presence of different cations is assessed by measuring the effective mean molecular area (

Electrochemical formation of high-energy species such as hydroxyl radicals in aqueous media is inefficient because oxidation of H2O to form O2 is a more thermodynamically favorable reaction. Boron-doped diamond (BDD) is widely used as an electrode material for generating •OH radicals because it has a very large kinetic overpotential for O2 production, thus increasing electrochemical efficiency for •OH production. Yet, the underlying mechanisms of O2 and •OH production at diamond electrodes are not well understood. We demonstrate that boron-doped diamond surfaces functionalized with hydrophobic, polyfluorinated molecular ligands (PF-BDD) have significantly higher electrochemical efficiency for •OH production compared with hydrogen-terminated (H-BDD), oxidized (O-BDD), or poly(ethylene ether)-functionalized (E-BDD) boron-doped diamond samples. Our measurements show that •OH production is nearly independent of surface functionalization and pH (pH = 7.4 vs 9.2), indicating that •OH is produced by oxidation of H2O in an outer-sphere electron-transfer process. In contrast, the total electrochemical current, which primarily produces O2, differs strongly between samples with different surface functionalizations, indicating an inner-sphere electron-transfer process. X-ray photoelectron spectroscopy measurements show that although both H-BDD and PF-BDD electrodes are oxidized over time, PF-BDD showed longer stability (≈24 h of use) than H-BDD. This work demonstrates that increasing surface hydrophobicity using perfluorinated ligands selectively inhibits inner-sphere oxidation to O2 and therefore provides a pathway to increased efficiency for formation of •OH via an outer-sphere process. The use of hydrophobic electrodes may be a general approach to increasing selectivity toward outer-sphere electron-transfer processes in aqueous media.

Molecular understanding of the impact of nanomaterials on cell membranes is critical for the prediction of effects that span environmental exposures to nanoenabled therapies. Experimental and computational studies employing phospholipid bilayers as model systems for membranes have yielded important insights but lack the biomolecular complexity of actual membranes. Here, we increase model membrane complexity by incorporating the peripheral membrane protein cytochrome c and studying the interactions of the resulting membrane systems with two types of anionic nanoparticles. Experimental and computational studies reveal that the extent of cytochrome c binding to supported lipid bilayers depends on anionic phospholipid number density and headgroup chemistry. Gold nanoparticles functionalized with short, anionic ligands or wrapped with an anionic polymer do not interact with silica-supported bilayers composed solely of phospholipids. Strikingly, when cytochrome c was bound to these bilayers, nanoparticles functionalized with short anionic ligands attached to model biomembranes in amounts proportional to the number of bound cytochrome c molecules. In contrast, anionic polymer-wrapped gold nanoparticles appeared to remove cytochrome c from supported lipid bilayers in a manner inversely proportional to the strength of cytochrome c binding to the bilayer; this reflects the removal of a weakly bound pool of cytochrome c, as suggested by molecular dynamics simulations. These results highlight the importance of the surface chemistry of both the nanoparticle and the membrane in predicting nano-bio interactions.

Citric acid is a widely used surface-modifying ligand for growth and processing of a variety of nanoparticles; however, the inability to easily prepare derivatives of this molecule has restricted the development of versatile chemistries for nanoparticle surface functionalization. Here, we report the design and synthesis of a citric acid derivative bearing an alkyne group and demonstrate that this molecule provides the ability to achieve stable, multidentate carboxylate binding to metal oxide nanoparticles, while also enabling subsequent multistep chemistry via the Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) reaction. The broad utility of this strategy for the modular functionalization of metal oxide surfaces was demonstrated by its application in the CuAAC modification of ZnO, Fe(2)O(3), TiO(2), and WO(3) nanoparticles.