We provide strong chemical and biophysical evidence that documents that branched amphiphilic peptides, BAPs, known to assemble into spherical nanoassemblies in solution, do assemble as peptide-bilayer-delimited capsules. These nanoassemblies are termed branched amphiphilic peptide capsules (BAPCs). BAPCs are taken up by cells and accumulate in the perinuclear region to persist there without apparent degradation. BAPCs also entrap small proteins and solutes and stably encapsulate α-particle-emitting radionuclides. We have devised a method utilizing thiol chemistry to conjugate these peptide sequences onto gold nanoparticles (≤5 nm) with the objective of demonstrating the assembly of these peptides into a bilayer. The peptides are initially assembled as a monolayer on the gold surface via interaction with cysteine residues on the peptide C-terminus in an organic solvent. The subsequent transition of these peptide-monolayerprotected gold nanoparticles to an aqueous solution in the presence of excess peptides led to the formation of the peptide bilayer on the gold surface. The approach was exploited further to produce bilayer-coated magnetic nanoparticles. The innovation described in this study provides a stable metallic nanoparticle−peptide conjugate system that will help to determine interactions of BAPs in a biological system, with relative ease, important for developing future applications such as simultaneous delivery and imaging of surface-bound molecules of interest.
A study of the viscoelastic relaxation in anhydrous liquid P 2 O 5 is reported. Properties of the time decay of the dynamic structure factor, including the average structural relaxation time and the stretching exponent, were obtained for temperatures from 850°C to near the glass transition ͑T g = 419°C͒ using photon correlation spectroscopy. Analysis indicates that P 2 O 5 is a strong glass-forming liquid but one that exhibits an abnormally nonexponential relaxation near T g . The viscoelastic behavior of P 2 O 5 is compared with that of its alkali-metalmodified metaphosphate counterparts NaPO 3 and LiPO 3 , as well as with the mechanical relaxation of chalcogenide glasses, to demonstrate common patterns in dynamical behavior presumably arising from changes in the average connectivity of the glass structure.
We report results of an extensive study of the structural relaxation occurring in mixed
alkali metaphosphate liquids obtained by photon correlation spectroscopy. Values for the
glass transition temperature, the fragility index, and the heterogeneity parameter (also
known as the Kohlrausch exponent) are extracted from the measurements and are all
shown to exhibit a mixed alkali effect wherein nonlinear variations with mixing occur. The
depression in the glass transition temperature is shown to be the direct result of mechanical
relaxations, present in the solid, which prematurely loosen the glass structure. A minimum
in the fragility index is believed to be an artifact of the resulting depression of the glass
transition temperature.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.