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METHODS FOR IDENTIFYING SMALL MOLEDULES THAT MODULATE PREMATURE TRANSLATION TERMINATION AND NONSENSE MEDIATED mRNA DECAY

机译:识别可调控过早翻译终止和无义介导的mRNA衰变的小分子的方法

摘要

The present invention relates to a method for screening and identifying compounds that modulate premature translation termination and/or nonsense-mediated messenger ribonucleic acid ('mRNA') by interacting with a preselected target ribonucleic acid ('RNA'). In particular, the present invention relates to identifying compounds that bind to regions of the 28S ribosomal RNA ('rRNA') and analogs thereof. Direct, noncompetitive binding assays are advantageously used to screen libraries of compounds for those that selectively bind to a preselected target RNA. Binding of target RNA molecules to a particular compound is detected using any physical method that measures the altered physical property of the target RNA bound to a compound. The structure of the compound attached to the labeled RNA is also determined. The methods used will depend, in part, on the nature of the library screened. The methods of the present invention provide a simple, sensitive assay for high-throughput screening of libraries of compounds to identify pharmaceutical leads.
机译:本发明涉及一种通过与预选的靶核糖核酸('RNA')相互作用来筛选和鉴定调节过早翻译终止和/或无义介导的信使核糖核酸('mRNA')的化合物的方法。特别地,本发明涉及鉴定与28S核糖体RNA('rRNA')的区域结合的化合物及其类似物。直接,非竞争性结合测定法有利地用于筛选化合物文库中与预选靶RNA选择性结合的化合物。使用测量结合于化合物的靶RNA的改变的物理性质的任何物理方法来检测靶RNA分子与特定化合物的结合。还确定了与标记的RNA连接的化合物的结构。所使用的方法将部分取决于所筛选库的性质。本发明的方法提供了一种简单,灵敏的测定方法,用于高通量筛选化合物文库以鉴定药物前导。

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