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In Situ Assembly and Screening of Enzyme Inhibitors with Surface-Tension Microarrays

机译:表面张力微阵列酶抑制剂的原位组装和筛选

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摘要

Microarray technology has been developed to address the growing number of assayed entities in the modern drug-discovery process. Generally, microarrays are produced by attaching one of the interacting components to the array surface. Subsequent screening of the surface-displayed entities against a liquid sample enables the identification of specifically interacting partners. Unfortunately, such a hetero-phase assay cannot be applied accurately to the majority of (bio)chemical reactions, which normally proceed in the solution phase. Gosalia and Diamond proposed a simple, yet elegant, solution to this problem by conducting enzymatic reactions in glycerol nanodroplets printed on the surface of a glass slide. This and related techniques have subsequently been used for profiling enzyme activities, inhibitors, and polymeric biomaterials.
机译:已经开发了微阵列技术来解决现代药物发现过程中越来越多的被分析实体的问题。通常,微阵列是通过将相互作用组分之一附着于阵列表面而产生的。随后针对液体样品对表面展示的实体进行筛选,可以鉴定出特定相互作用的伴侣。不幸的是,这种异相分析不能准确地应用于通常在溶液相中进行的大多数(生物)化学反应。 Gosalia和Diamond提出了一种简单而优雅的解决方案,通过在载玻片表面上印刷的甘油纳米滴中进行酶促反应。该技术和相关技术随后已用于分析酶活性,抑制剂和聚合生物材料。

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