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SCAN——一种用于检测小分子与RNA靶点结合的高通量检测方法。

SCAN--a high-throughput assay for detecting small molecule binding to RNA targets.

作者信息

Baugh Chris, Wang Shaohui, Li Bin, Appleman James R, Thompson Peggy A

机构信息

Department of Biology, Anadys Pharmaceuticals, Inc., San Diego, California 92121, USA.

出版信息

J Biomol Screen. 2009 Mar;14(3):219-29. doi: 10.1177/1087057108330111. Epub 2009 Feb 11.

Abstract

A novel optical-based high-throughput screening technology has been developed for increasing the rate of discovering chemical leads against RNA targets. SCAN ( Screen for Compounds with Affinity for Nucleic Acids) is an affinity-based assay that identifies small molecules that bind and recognize structured RNA elements. This technology provides the opportunity to conduct high-throughput screening of a new class of targets-RNA. SCAN offers many attractive features including a simple homogeneous format, low screening costs, and the ability to use common laboratory equipment. A SCAN assay was developed for the HCV IRES Loop IIId RNA domain. A high-throughput screen of our entire compound library resulted in the identification of small molecule ligands that bind to Loop IIId. The Z' values were greater than 0.8, showing this to be a robust high-throughput screening assay. A correlation between SCAN EC50 and KD values is reported suggesting the ability to use the assay for compound optimization.

摘要

为了提高针对RNA靶点发现化学先导物的速率,已经开发出一种新型的基于光学的高通量筛选技术。SCAN(筛选与核酸具有亲和力的化合物)是一种基于亲和力的检测方法,可识别与结构化RNA元件结合并识别的小分子。该技术为对一类新靶点——RNA进行高通量筛选提供了机会。SCAN具有许多吸引人的特性,包括简单的均相形式、低筛选成本以及使用普通实验室设备的能力。针对丙型肝炎病毒内部核糖体进入位点(IRES)Loop IIId RNA结构域开发了一种SCAN检测方法。对我们整个化合物库进行高通量筛选,结果鉴定出了与Loop IIId结合的小分子配体。Z'值大于0.8,表明这是一种稳健的高通量筛选检测方法。报道了SCAN的半数有效浓度(EC50)与解离常数(KD)值之间的相关性,表明该检测方法可用于化合物优化。

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