Two-dimensionally well-ordered multilayer structures in thin films of a brush polypeptide

In this study, we report the first production of two-dimensionally well-ordered molecular multilayers (i.e., with a well-defined molecular lamellar structure) based on the antiparallel beta-sheet chain conformation in thin films of a brush polypeptide, poly(S-n-hexadecyl-dl-homocysteine) (PHHC), through the use of a simple spin-coating process and the quantitative structural and property analysis of the thin films using a grazing incidence X-ray scattering technique combined with Fourier transform infrared spectroscopy and differential scanning calorimetry. These analyses provide detailed information about the structure and molecular conformation of the self-assembled lamellae in the PHHC thin film, which is not easily obtained using conventional techniques. Moreover, we used the in situ measurements carried out at various temperatures and the data analyses to establish mechanisms for the evolution of the self-assembled lamellar structures in the film and for their melting. In addition, we propose molecular structure models of the PHHC polymer molecules in the thin film at various temperatures.     

A Paper‐Based Platform for Long‐Term Deposition of Nanoparticles with Exceptional Redispersibility,Stability, and Functionality

Although nanoparticles (NPs) can be carefully engineered to have maximal stability and functionality desirable for use in diverse applications, they are generally not suitable for long‐term storage in solution. It is also difficult to store NPs in a dry state because dried NPs generally become aggregated and cannot easily be redispersed. Thus, a new strategy allowing long‐term storage of NPs with high stability, redispersibility, and functionality is highly demanded. By passivating the 13 nm gold nanoparticle (AuNP) surface with stabilizing agents and treating a paper substrate with both bovine serum albumin and sucrose after coating with a hydrophobic polyvinyl butyral layer, it is possible to fully redisperse (≈100%) dried AuNPs with colloidal stability comparable to that of as‐prepared AuNPs. Furthermore, AuNPs physically stabilized with polyvinylpyrrolidone can react with thiol‐containing compounds, such as 1,4‐dithiothreitol (DTT). Taking advantage of the oxidation reaction of hypochlorous acid with DTT, it is possible to demonstrate a paper‐based colorimetric sensor for detection of residual chlorine in water. Since this strategy is applicable to large‐sized AuNPs (30–90 nm), silver NPs, oleic acid‐capped magnetic NPs, and cetrimonium bromide‐passivated gold nanorods, it can be used for diverse NPs requiring long‐term storage for many applications.     

Simple fabrication of a smart microarray of polystyrene microbeads for immunoassay

We describe a simple method to fabricate an array of polystyrene microbeads (PS μbeads) conjugated with an elastin-like polypeptide (ELP) on a glass surface using a removable polymer template (RPT). A thin layer of adhesive was spun-cast on glass and cured by UV radiation. Micropatterns of an RPT were then transferred onto the surface by microcontact printing. The adhesion of PS μbeads on the surface depended on the adhesion performance of the adhesive layer, which could be adjusted by irradiation time. An array of PS μbeads conjugated with ELP was used for a smart immunoassay of prostate-specific antigen (PSA), a cancer marker. By controlling the phase transition of ELP molecules, PSA molecules were selectively adhered or released from the bead surface. The selective and reversible binding of PSA molecules on the bead surface was characterized with fluorescence microscopy.