Deondre Jordan, Mo Yang, John S. Schneekloth Jr.
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引用次数: 3
Abstract
Small molecule microarray (SMM) technology has become a powerful tool used in high-throughput screening for target-based drug discovery. One area in which SMMs have found use is the identification of small molecule ligands for RNA. RNAs with unique secondary or tertiary three-dimensional structures are considered to be attractive targets for small molecules. Complex RNA structures can form hydrophobic pockets suitable for small molecule binding, representing an opportunity for developing novel therapeutics. Our lab has previously taken a target-based approach, screening a single target against many small molecules on an SMM platform. Here, we report a screening protocol for SMMs to investigate multiple RNAs simultaneously using multi-color imaging. By introducing a mixture containing different fluorophore-labeled RNAs, the fluorescence signal of each binding event can be observed simultaneously. Thus, the specificity of a hit compound binding to one RNA target over other highly abundant RNAs (such as tRNA or rRNA) can be easily evaluated. © 2020 Wiley Periodicals LLC.
Basic Protocol: RNA screening on SMMs by multi-color imaging
Support Protocol 1: Preparation of SMM slides
Support Protocol 2: Fluorophore labeling of RNA through maleimide chemistry
三色成像可以同时筛选小分子微阵列上的多个RNA靶标
小分子微阵列(SMM)技术已成为靶向药物高通量筛选的有力工具。smm的一个应用领域是鉴定RNA的小分子配体。具有独特的二级或三级三维结构的rna被认为是小分子的有吸引力的靶标。复杂的RNA结构可以形成适合小分子结合的疏水口袋,这为开发新的治疗方法提供了机会。我们的实验室以前采用了一种基于靶标的方法,在SMM平台上筛选单个靶标对抗许多小分子。在这里,我们报告了一种SMMs的筛选方案,可以同时使用多色成像来研究多个rna。通过引入含有不同荧光团标记rna的混合物,可以同时观察到每个结合事件的荧光信号。因此,可以很容易地评估一个命中化合物与一个RNA靶标结合的特异性,而不是其他高度丰富的RNA(如tRNA或rRNA)。©2020 Wiley期刊有限责任公司基本协议:RNA筛选的SMMs通过多色成像支持协议1:SMM幻灯片的制备支持协议2:通过马来酰亚胺化学RNA的荧光基团标记
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