Nathalie Y-Wa Tang

Nanostructured phospholipid membranes

This review describes a simple high-throughput method for producing laterally nanostructured monolayer and bilayer films on planar surfaces based on the Langmuir-Blodgett transfer of a phase-separated phospholipid mixture from the air/water interface to a solid support. Applications of the patterned lipid films to spatially direct the adsorption of proteins and to demonstrate stereoselective enzyme lithography are reviewed.

Cellular imaging by targeted assembly of hot-spot SERS and photoacoustic nanoprobes using split-fluorescent protein scaffolds

The in cellulo assembly of plasmonic nanomaterials into photo-responsive probes is of great interest for many bioimaging and nanophotonic applications but remains challenging with traditional nucleic acid scaffolds-based bottom-up methods. Here, we address this quandary using split-fluorescent protein (FP) fragments as molecular glue and switchable Raman reporters to assemble gold or silver plasmonic nanoparticles (NPs) into photonic clusters directly in live cells. When targeted to diffusing surface biomarkers in cancer cells, the NPs self-assemble into surface-enhanced Raman-scattering (SERS) nanoclusters having hot spots homogenously seeded by the reconstruction of full-length FPs. Within plasmonic hot spots, autocatalytic activation of the FP chromophore and near-field amplification of its Raman fingerprints enable selective and sensitive SERS imaging of targeted cells. This FP-driven assembly of metal colloids also yields enhanced photoacoustic signals, allowing the hybrid FP/NP nanoclusters to serve as contrast agents for multimodal SERS and photoacoustic microscopy with single-cell sensitivity.Traditional methods for the assembly of plasmonic nanoparticles into photo-responsive probes suffer from multiple problems. Here the authors use split fluorescent protein fragments as molecular glue to form stable nanoclusters for surface enhanced Raman scattering and photoacoustic imaging in live cells.

Fano resonances in the midinfrared spectra of single-walled carbon nanotubes.

This work revisits the physics giving rise to the carbon nanotube phonon bands in the midinfrared. Our measurements of doped and undoped samples of single-walled carbon nanotubes in Fourier transform infrared spectroscopy show that the phonon bands exhibit an asymmetric line shape and that their effective cross section is enhanced upon doping. We relate these observations to electron-phonon coupling or, more specifically, to a Fano resonance phenomenon. We note that the dopant-induced intraband (not interband) continuum couples strongly to the phonon modes, and that defects created on the sidewall are scattering centers that increase the spectral amplitude of the resonance.

Self-Patterned Mixed Phospholipid Monolayers for the Spatially Selective Deposition of Metals

Metal-reactive organosulfur groups were patterned onto mica and silicon surfaces by dewetting instabilities during the Langmuir-Blodgett (LB) deposition of phase-separated mixed phospholipid monolayers. Monolayers were formed from binary mixtures of dipalmitoylphosphatidylcholine (DPPC), dilauroylphosphatidylcholine (DLPC), and their ω-methyldisulfide-dialkylphosphatidylcholine analogues, DSDPPC and DSDLPC. Patterns of highly parallel stripes of condensed DPPC or DSDPPC, protruding by 0.7-0.9 nm from a fluid matrix of DLPC or DSDLPC, were observed over areas extending at least 30 × 30 μm(2) in the LB films. The average stripe width varied from ca. 150 to 500 nm, depending on the lipid composition and deposition pressure. X-ray photoelectron spectroscopy confirmed that the phospholipid-monolayer-bound methydisulfides react with Au vapor to form a gold-thiolate species. The adsorption of thermally evaporated Au, Ag, and Cu onto DSDPPC/DLPC and DPPC/DSDLPC patterns was investigated by field emission gun scanning electron microscopy (FEGSEM) and atomic force microscopy (AFM). A change in phase contrast is observed in FEGSEM and AFM over the methyldisulfide-functionalized areas following metal deposition due to metal-thiolate bond formation. An increase in step height between the DSDPPC stripes and nonfunctionalized DLPC background following metal deposition, as well as the resistance of the metal-coated DSDPPC or DSDLPC regions to detergent extraction from the surface, attest to a selective metallization of the pattern. Our results indicate that the preferential adsorption of vapor-deposited metal onto the ω-methyldisulfide-terminated phase occurs at submonolayer coverages. The chemical reactivity exhibited by the organosulfur-modified phospholipid LB films make these templates potentially interesting for the fabrication of solid-supported patterns of metal nanostructures.