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基于 RNA 的捕获-SELEX 用于小分子结合适体的筛选。

RNA-based Capture-SELEX for the selection of small molecule-binding aptamers.

机构信息

Department of Biology, TU Darmstadt, Schnittspahnstrasse 10, 64287 Darmstadt, Germany.

Department of Biology, TU Darmstadt, Schnittspahnstrasse 10, 64287 Darmstadt, Germany.

出版信息

Methods. 2019 May 15;161:10-15. doi: 10.1016/j.ymeth.2019.04.004. Epub 2019 Apr 4.

Abstract

Despite their wide applicability, the selection of small molecule-binding RNA aptamers with both high affinity binding and specificity is still challenging. Aptamers that excel at both binding and structure switching are particularly rare and difficult to find. Here, we present the protocol of a Capture-SELEX that specifically allows the in vitro selection of small-molecule binding aptamers, which are essential building blocks for the design process of synthetic riboswitches and biosensors. Moreover, we provide a comparative overview of our proposed methodology versus alternative in vitro selection protocols with a special focus on the design of the pool. Finally, we have included detailed notes to point out useful tips and pitfalls for future application.

摘要

尽管小分子结合 RNA 适体具有广泛的适用性,但要同时具有高亲和力结合和特异性的选择仍然具有挑战性。在结合和结构转换方面都表现出色的适体尤其罕见且难以找到。在这里,我们介绍了一种捕获-SELEX 方法,该方法专门允许体外选择小分子结合适体,这些适体是合成核糖开关和生物传感器设计过程的基本构建块。此外,我们还提供了对我们提出的方法与其他体外选择方案的比较概述,特别关注池的设计。最后,我们包含了详细的说明,指出了未来应用的有用提示和陷阱。

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