Abstract
For the first time, a microchannel was photochemically patterned with a functional linker. This simple method was developed for the site-specific attachment of DNA via this linker onto silicon oxide surfaces (e.g., fused silica and borosilicate glass), both onto a flat surface and onto the inside of a fused silica microchannel. Sharp boundaries in the micrometer range between modified and unmodified zones were demonstrated by the attachment of fluorescently labeled DNA oligomers. Studies of repeated hybridization- dehybridization cycles revealed selective and reversible binding of cDNA strands at the explicit locations. On average, ∼7x 1011 fluorescently labeled DNA molecules were hybridized per square centimeter. The modified surfaces were characterized with X-ray photoelectron spectroscopy, infrared microscopy, static contact angle measurements, confocal laser scanning microscopy, and fluorescence detection (to quantify the attachment of the fluorescently labeled DNA). © 2009 American Chemical Society.
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CITATION STYLE
Vong, T., Maat, J. T., Van Beek, T. A., Van Lagen, B., Giesbers, M., Van Hest, J. C. M., & Zuilhof, H. (2009). Site-specific immobilization of DNA in glass microchannels via photolithography. Langmuir, 25(24), 13952–13958. https://doi.org/10.1021/la901558n
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