Section of Structural and Synthetic Biology, Department of Infectious Disease , Imperial College London , London SW7 2AZ , U.K.
London Biofoundry , Imperial College Translation & Innovation Hub , White City Campus, 80 Wood Lane , London W12 0BZ , U.K.
ACS Synth Biol. 2020 Jan 17;9(1):144-156. doi: 10.1021/acssynbio.9b00437. Epub 2020 Jan 3.
The field of mammalian synthetic biology is expanding quickly, and technologies for engineering large synthetic gene circuits are increasingly accessible. However, for mammalian cell engineering, traditional tissue culture methods are slow and cumbersome, and are not suited for high-throughput characterization measurements. Here we have utilized mammalian cell-free protein synthesis (CFPS) assays using HeLa cell extracts and liquid handling automation as an alternative to tissue culture and flow cytometry-based measurements. Our CFPS assays take a few hours, and we have established optimized protocols for small-volume reactions using automated acoustic liquid handling technology. As a proof-of-concept, we characterized diverse types of genetic regulation in CFPS, including T7 constitutive promoter variants, internal ribosomal entry sites (IRES) constitutive translation-initiation sequence variants, CRISPR/dCas9-mediated transcription repression, and L7Ae-mediated translation repression. Our data shows simple regulatory elements for use in mammalian cells can be quickly prototyped in a CFPS model system.
哺乳动物合成生物学领域发展迅速,工程大型合成基因回路的技术也越来越容易获得。然而,对于哺乳动物细胞工程来说,传统的组织培养方法既缓慢又繁琐,不适合高通量的特征测量。在这里,我们利用使用 HeLa 细胞提取物的哺乳动物无细胞蛋白合成 (CFPS) 测定法和液体处理自动化作为组织培养和基于流式细胞术的测量的替代方法。我们的 CFPS 测定法只需要几个小时,并且我们已经使用自动化声控液体处理技术为使用小体积反应建立了优化的方案。作为概念验证,我们在 CFPS 中对不同类型的基因调控进行了表征,包括 T7 组成型启动子变体、内部核糖体进入位点 (IRES) 组成型翻译起始序列变体、CRISPR/dCas9 介导的转录抑制和 L7Ae 介导的翻译抑制。我们的数据表明,可用于哺乳动物细胞的简单调控元件可在 CFPS 模型系统中快速原型化。