Direct Probes of 4 nm Diameter Gold Nanoparticles Interacting with Supported Lipid Bilayers

TitleDirect Probes of 4 nm Diameter Gold Nanoparticles Interacting with Supported Lipid Bilayers
Publication TypeJournal Article
Year of Publication2015
AuthorsTroiano, JM, Olenick, LL, Kuech, TR, Melby, ES, Hu, DH, Lohse, SE, Mensch, AC, Dogangun, M, Vartanian, AM, Torelli, MD, Ehimiaghe, E, Walter, SR, Fu, L, Anderton, CR, Zhu, ZH, Wang, HF, Orr, G, Murphy, CJ, Hamers, RJ, Pedersen, JA, Geiger, FM
JournalJournal of Physical Chemistry C
Volume119
Start Page534
Pagination534-546
Date Published01/2015
ISBN Number1932-7447
Keywords2nd-harmonic, atomic-force microscopy, double-layer, generation, interfacial water-structure, magnesium-ions, nano-bio interface, phospholipid-bilayers, silica/water interfaces, spherical nucleic-acids, sum-frequency
Abstract

This work presents molecular-level investigations of how well-characterized silica-supported phospholipid bilayers formed from either pure DOPC or a 9:1 mixture of DOPC:DOTAP interact with positively and negatively charged 4 nm gold metal nanoparticles at pH 7.4 and NaCl concentrations ranging from 0.001 to 0.1 M. Second harmonic generation (SHG) charge screening measurements indicate the supported bilayers carry a negative interfacial potential. Resonantly enhanced SHG measurements probing electronic transitions within the gold core of the nanoparticles show the particles interact irreversibly with the supported bilayers at a range of concentrations. At 0.1 M NaCl, surface coverages for the particles functionalized with the negatively charged ligand mercaptopropionic acid (MPA) or wrapped in the cationic polyelectrolyte poly(allylamine) hydrochloride (PAH) are estimated from a joint analysis of QCM-D, XPS, AFM, and ToF-SIMS to be roughly 1 x 10 (7) and 1 x 10 (11) particles cm(2), respectively. Results from complementary SHG charge screening experiments point to the possibility that the surface coverage of the MPA-coated particles is more limited by interparticle Coulomb repulsion due to the charges within their hydrodynamic volumes than with the PAH-wrapped particles. Yet, SHG adsorption isotherms indicate that the interaction strength per particle is independent of ionic strength and particle coating, highlighting the importance of multivalent interactions. H-1 NMR spectra of the lipids within vesicles suspended in solution show little change upon interaction with either particle type but indicate loosening of the gold-bound PAH polymer wrapping upon attachment to the vesicles. The thermodynamic, spectroscopic, and electrostatic data presented here may serve to benchmark experimental and computational studies of nanoparticle attachment processes at the nanobio interface.

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