AFM-based force spectroscopy on polystyrene brushes: effect of brush thickness on protein adsorption.

Herein we present a study on nonspecific binding of proteins at highly dense packed hydrophobic polystyrene brushes. In this context, an atomic force microscopy tip was functionalized with concanavalin A to perform single-molecule force spectroscopy measurements on polystyrene brushes with thicknesses of 10 and 60 nm, respectively. Polystyrene brushes with thickness of 10 nm show an almost two times stronger protein adsorption than brushes with a thickness of 60 nm: 72 pN for the thinner and 38 pN for the thicker layer, which is in qualitative agreement with protein adsorption studies conducted macroscopically by fluorescence microscopy.

Coat thickness dependent adsorption of hydrophobic molecules at polymer brushes.

We study the adsorption properties of hydrophobic test particles at polymer brushes with different coat thicknesses via mesoscopic dissipative particle dynamics simulations. Our findings indicate stronger free energies of adsorption at thin polymer brushes. The reason for this difference is mainly given by entropic contributions due to different elastic deformations of the coatings. The numerical findings are supported by analytical calculations and are in good qualitative agreement to experimental fluorescence intensity results.

Chemical surface modification of self-assembled monolayers by radical nitroxide exchange reactions.

This article describes the application of nitroxide exchange reactions of surface-bound alkoxyamines as a tool for reversible chemical modification of self-assembled monolayers (SAMs). This approach is based on radical chemistry, which allows for introduction of various functional groups and can be used to reversibly introduce functionalities at surfaces. To investigate the scope of this surface chemistry, alkoxyamines with different functionalities were synthesized and were then applied to the immobilization of, for example, dyes, sugars, or biotin. Surface analysis was carried out by contact angle, X-ray photoelectron spectroscopy, and fluorescence microscopy measurements. The results show that this reaction is highly efficient, reversible, and mild and allows for immobilization of various sensitive functional groups. In addition, Langmuir-Blodgett lithography was used to generate structured SAMs. Site-selective immobilization of a fluorescent dye could be achieved by nitroxide exchange reactions.

On-surface azide-alkyne cycloaddition on Au(111).

We present [3 + 2] cycloaddition reactions between azides and alkynes on a Au(111) surface at room temperature and under ultrahigh vacuum conditions. High-resolution scanning tunneling microscopy images reveal that these on-surface cycloadditions occur highly regioselectively to form the corresponding 1,4-triazoles. Density functional theory simulations confirm that the reactions can occur at room temperature, where the Au(111) surface does not participate as a catalytic agent in alkyne C-H activation but acts solely as a two-dimensional constraint for the positioning of the two reaction partners. The on-surface azide-alkyne cycloaddition offers great potential toward the development and fabrication of functional organic nanomaterials on surfaces.

Development of a two-dimensional virtual-pixel X-ray imaging detector for time-resolved structure research.

An interpolating two-dimensional X-ray imaging detector based on a single-photon counter with gas amplification by GEM (gas electron multiplier) structures is presented. The detector system can be used for time-resolved structure research down to the micro s time domain. The prototype detector has been tested at the SAXS (small-angle X-ray scattering) beamline at ELETTRA synchrotron light source with a beam energy of 8 keV. The imaging performance is examined with apertures and standard diffraction targets. Finally, the application in a time-resolved lipid temperature-jump experiment is presented.