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Spatially-Addressable Immobilization of Macromolecules on Solid Supports

机译:大分子在固体支持物上的空间可寻址固定化

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摘要

A method is described for immobilization of receptors, antibodies, or other macromolecules at precise locations on solid substrates. We have combined photolithographic techniques with the use of a "caged" biotin analogue that has been covalently linked to the substrate surface. Exposure to near UV light through a photolithographic mask yields biotin sites for streptavidin binding. Biotinylated macromolecules are then immobilized via a biotin-streptavidin-biotin bridge. Molecules may be attached at selected locations by carrying out repeated rounds of exposure, streptavidin binding, and application of the biotinylated reagent. We have demonstrated the immobilization of fluorescein-streptavidin molecules in 500 μm x 500 μm sites, and the localization of two biotinylated antibodies at different sites on a planar substrate surface. We anticipate that the technique will prove useful in drug screening, diagnostics, and biosensor applications.
机译:描述了一种将受体,抗体或其他大分子固定在固体基质上精确位置的方法。我们将光刻技术与已共价连接至基质表面的“笼状”生物素类似物相结合。通过光刻掩模暴露于近紫外光下会产生生物素位点,以与链霉亲和素结合。然后通过生物素-链霉亲和素-生物素桥固定生物素化的大分子。分子可以通过进行多次暴露,抗生蛋白链菌素结合以及生物素化试剂的应用来重复地附着在选定的位置。我们已经证明了荧光素-链霉亲和素分子的固定化在500μmx 500μm的位置,以及两种生物素化抗体在平面基质表面上不同位置的定位。我们预计该技术将在药物筛选,诊断和生物传感器应用中被证明是有用的。

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