Department of Biology, Technical University Darmstadt, Darmstadt, Germany.
Centre of Synthetic Biology, Technical University Darmstadt, Darmstadt, Germany.
Methods Mol Biol. 2022;2518:157-177. doi: 10.1007/978-1-0716-2421-0_10.
Synthetic riboswitches are a promising tool for conditional gene expression. In vitro selected aptamers used as binding domains for the design of RNA-based switches have to exhibit excellent binding affinity as well as ligand binding-induced structural changes. Selection via Capture-SELEX favors the enrichment of aptamers which exhibit both characteristics. For the Capture-SELEX, an RNA pool is used that gets immobilized onto a capture oligonucleotide by hybridization. Addition of the ligand frees the aptamers by their binding to the ligand, resulting in the release from the capture oligonucleotide through structural changes. These sequences get reverse transcribed, PCR amplified, and used for the following selection rounds. In this publication, we present a detailed protocol for Capture-SELEX, followed by screening in yeast to identify aptamers suitable for the design of synthetic riboswitches.
合成核糖开关是一种有前途的条件基因表达工具。在体外选择的适体作为基于 RNA 的开关设计的结合结构域,必须表现出优异的结合亲和力以及配体结合诱导的结构变化。通过Capture-SELEX 的选择有利于富集同时具有这两种特性的适体。对于 Capture-SELEX,使用一个 RNA 池,该 RNA 池通过杂交固定在捕获寡核苷酸上。配体的加入通过与配体的结合来释放适体,导致通过结构变化从捕获寡核苷酸上释放出来。这些序列被反转录、PCR 扩增,并用于后续的选择轮次。在本出版物中,我们提供了一个详细的 Capture-SELEX 方案,然后在酵母中进行筛选,以鉴定适合合成核糖开关设计的适体。