A strategy has been developed for the grafting of poly(ethylene glycol) (PEG) monolayers onto the atomically flat Si(111) surface. This process involves the direct interaction of the HO-functional group on PEG with a chlorine-terminated silicon surface. The resulting monolayers show exceptional flatness, with mean roughness on the angstrom scale. Film thickness is determined by ellipsometry, X-ray photoelectron spectroscopy, and atomic force microscopy. Results for different molecular weights reveal that the grafted PEG molecules are in a brushlike configuration at low molecular weight (MW = 200, 300) and a more coil-like configuration at higher molecular weight (MW = 1000, 2000). The surface density of grafted PEG molecules is significantly higher than those reported in the literature and decreases with increasing molecular weight, from 92% at MW = 300 to 35% at MW = 2000. Both the brushlike and the coil-like configurations show excellent properties of protein resistance.
A high-density poly(ethylene glycol) (PEG)-coated Si(111) surface is used for the immobilization of polyhistidine-tagged protein molecules. This process features a number of properties that are highly desirable for protein microarray technology: (i) minimal nonspecific protein adsorption; (ii) highly uniform surface functionality; (iii) controlled protein orientation; and (iv) highly specific immobilization reaction without the need of protein purification. The high-density PEG-coated silicon surface is obtained from the reaction of a multi-arm PEG (mPEG) molecule with a chlorine terminated Si(111) surface to give a mPEG film with thickness of 5.2 nm. Four out of the eight arms on each immobilized mPEG molecule are accessible for linking to the chelating iminodiacetic acid (IDA) groups for the binding of Cu(2+) ions. The resulting Cu(2+)-IDA-mPEG-Si(111) surface is shown to specifically bind 6x histidine-tagged protein molecules, including green fluorescent protein (GFP) and sulfotransferase (ST), but otherwise retains its inertness towards nonspecific protein adsorption. We demonstrate a particular advantage of this strategy: the possibility of protein immobilization without the need of prepurification. Surface concentrations of relevant chemical species are quantitatively characterized at each reaction step by X-ray photoelectron spectroscopy (XPS). This kind of quantitative analysis is essential in tuning surface concentration and chemical environment for optimal sensitivity in probe-target interaction.
A simple and easy method is demonstrated for the fabrication of the shape controllable micro-lenses, which are widely used in biomedical systems for improving the image quality as their ability to efficiently focus light into the devices. The micro-lenses were drop on demand printed on the glass micro-holes based on a simple drop on demand printing technique. The shape controllable micro-lenses with a fixed diameter resulting from boundary confinement effect of the micro-holes and the surface wetting conditions are controlled by printing different numbers of drops per micro-lens. The influence of the geometrical shape changes on the optical properties is also investigated. The micro-lens array with different numerical apertures (NA) can be fabricated by controlling the number of drops of the micro-holes as the boundary confinement and hydrophobic effect of the micro-holes.
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