We describe for the first time the crystallization in thin films of a DNA copolymer composed of a low molecular weight chitosan backbone to which a sequence of nucleic acids is grafted (chitosan-g-ssDNA). As assessed by atomic force microscopy, optical microscopy and spectroscopy, crystallization occurs due to intermolecular hydrogen bonding in which the nucleic acid strands engage. The morphology of the crystals depends on the affinity for the surface of the polymer segments that compose the DNA copolymer hybrid. The nucleic acids adsorb on mica and silica on which side-branched structures are observed whereas chitosan interacts preferentially with gold, and dendritic crystals are assembled. Attenuated total reflectance infrared spectroscopy supports the high ordering of the structure and the establishment of strong intermolecular interactions by hydrogen bonding.

A high-throughput approach to fabricate gold nanowires on surfaces with a lipid nanotube template is demonstrated. Streptavidin-coated gold nanoparticles are attached to the biotin-tagged lipid nanotubes. After the chemical fixation, the samples are dried and treated with oxygen plasma to remove the organic template and connect the particles. The created nanowires are characterized by cryo-transmission electron microscopy, atomic force microscopy, and electrical measurements.

Conventional lipid-tube formation is based on either a tube phase of certain lipids or the shape transformation of lamellar structures by applying a point load. In the present study, lipid blocks in inverted hexagonal phase made of 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE) were shown to protrude lipid nanotubes upon a fluid-dynamic flow on polyelectrolyte-functionalized surfaces in physiological buffer solution. The outer diameter of the tubes is 19.1 ± 4.5 nm and their lengths are up to several hundred micrometers. The method described enables the alignment and patterning of lipid nanotubes into various (including curvy) shapes with a microfluidic system.