Mohsen Michael G, Breaker Ronald R
Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06511, USA.
Howard Hughes Medical Institute, Yale University, New Haven, CT 06511, USA.
Bio Protoc. 2023 Jul 5;13(13):e4775. doi: 10.21769/BioProtoc.4775.
Engineered aptamers for new compounds are typically produced by using in vitro selection methods. However, aptamers that are developed in vitro might not function as expected when introduced into complex cellular environments. One approach that addresses this concern is the design of initial RNA pools for selection that contain structural scaffolds from naturally occurring riboswitch aptamers. Here, we provide guidance on design and experimental principles for developing riboswitch-inspired aptamers for new ligands. The in vitro selection protocol (based on Capture-SELEX) is generalizable to diverse RNA scaffold types and amenable to multiplexing of ligand candidates. We discuss strategies to avoid propagation of selfish sequences that can easily dominate the selection. We also detail the identification of aptamer candidates using next-generation sequencing and bioinformatics, and subsequent biochemical validation of aptamer candidates. Finally, we describe functional testing of aptamer candidates in bacterial cell culture. Key features Develop riboswitch-inspired aptamers for new ligands using in vitro selection. Ligand candidates can be multiplexed to conserve time and resources. Test aptamer candidates in bacterial cells by grafting the aptamer back onto its expression platform.
用于新化合物的工程适配体通常通过体外筛选方法产生。然而,体外开发的适配体在引入复杂的细胞环境时可能无法按预期发挥作用。解决这一问题的一种方法是设计用于筛选的初始RNA文库,其中包含来自天然存在的核糖开关适配体的结构支架。在这里,我们为开发针对新配体的核糖开关启发的适配体提供设计和实验原理方面的指导。体外筛选方案(基于Capture-SELEX)可推广到多种RNA支架类型,并适用于配体候选物的多重筛选。我们讨论了避免自私序列传播的策略,这些自私序列很容易在筛选中占据主导地位。我们还详细介绍了使用下一代测序和生物信息学鉴定适配体候选物,以及随后对适配体候选物进行生化验证的过程。最后,我们描述了在细菌细胞培养中对适配体候选物进行功能测试的方法。关键特性 使用体外筛选开发针对新配体的核糖开关启发的适配体。 可以对配体候选物进行多重筛选以节省时间和资源。 通过将适配体嫁接到其表达平台上,在细菌细胞中测试适配体候选物。