7 research outputs found
Synthesis and characterization of mixed ligand chiral nanoclusters
Chiral mixed ligand silver nanoclusters were synthesized in the presence of a chiral and an achiral ligand. The ratio of the ligands was changed to track the formation of these clusters. While the chiral ligand lead to nanoparticles, Presence of the achiral ligand induced the formation of nanoclusters with chiral properties
Synthesis and Characterization of Amphiphilic Gold Nanoparticles
Gold nanoparticles covered with a mixture of 1-octanethiol (OT) and 11-mercapto-1-undecane sulfonic acid (MUS) have been extensively studied because of their interactions with cell membranes, lipid bilayers, and viruses. The hydrophilic ligands make these particles colloidally stable in aqueous solutions and the combination with hydrophobic ligands creates an amphiphilic particle that can be loaded with hydrophobic drugs, fuse with the lipid membranes, and resist nonspecific protein adsorption. Many of these properties depend on nanoparticle size and the composition of the ligand shell. It is, therefore, crucial to have a reproducible synthetic method and reliable characterization techniques that allow the determination of nanoparticle properties and the ligand shell composition. Here, a one-phase chemical reduction, followed by a thorough purification to synthesize these nanoparticles with diameters below 5 nm, is presented. The ratio between the two ligands on the surface of the nanoparticle can be tuned through their stoichiometric ratio used during synthesis. We demonstrate how various routine techniques, such as transmission electron microscopy (TEM), nuclear magnetic resonance (NMR), thermogravimetric analysis (TGA), and ultraviolet-visible (UV-Vis) spectrometry, are combined to comprehensively characterize the physicochemical parameters of the nanoparticles
Calcium-triggered fusion of lipid membranes is enabled by amphiphilic nanoparticles
Lipid membrane fusion is an essential process for a number of critical biological functions. The overall process is thermodynamically favorable but faces multiple kinetic barriers along the way. Inspired by nature's engineered proteins such as SNAP receptor [soluble N-ethylmale-imide-sensitive factor-attachment protein receptor (SNARE)] complexes or viral fusogenic proteins that actively promote the development of membrane proximity, nucleation of a stalk, and triggered expansion of the fusion pore, here we introduce a synthetic fusogen that can modulate membrane fusion and equivalently prime lipid membranes for calcium-triggered fusion. Our fusogen consists of a gold nanoparticle functionalized with an amphiphilic monolayer of alkanethiol ligands that had previously been shown to fuse with lipid bilayers. While previous efforts to develop synthetic fusogens have only replicated the initial steps of the fusion cascade, we use molecular simulations and complementary experimental techniques to demonstrate that these nanoparticles can induce the formation of a lipid stalk and also drive its expansion into a fusion pore upon the addition of excess calcium. These results have important implications in general understanding of stimuli-triggered fusion and the development of synthetic fusogens for biomedical applications.U.S. Department of Energy (Contract DE-FG02-97ER25308)National Science Foundation (Contract TG-DMR130042)U. S. Army Research Office (Contract W911NF-13-D-0001
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The
development of synthetic nanomaterials that could embed within,
penetrate, or induce fusion between membranes without permanent disruption
would have great significance for biomedical applications. Here we
describe structure–function relationships of highly water-soluble
gold nanoparticles comprised of an ∼1.5–5 nm diameter
metal core coated by an amphiphilic organic ligand shell, which exhibit
membrane embedding and fusion activity mediated by the surface ligands.
Using an environment-sensitive dye anchored within the ligand shell
as a sensor of membrane embedding, we demonstrate that particles with
core sizes of ∼2–3 nm are capable of embedding within
and penetrating fluid bilayers. At the nanoscale, these particles
also promote spontaneous fusion of liposomes or spontaneously embed
within intact liposomal vesicles. These studies provide nanoparticle
design and selection principles that could be used in drug delivery
applications, as membrane stains, or for the creation of novel organic/inorganic
nanomaterial self-assemblies