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高通量调控元件的无细胞蛋白合成和液滴微流控原型设计与分析。

High-Throughput Regulatory Part Prototyping and Analysis by Cell-Free Protein Synthesis and Droplet Microfluidics.

机构信息

Broad Institute of MIT and Harvard, Cambridge, 415 Main Street, Cambridge, Massachusetts 02142, United States.

Department of Chemical and Biological Engineering, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208-3120, United States.

出版信息

ACS Synth Biol. 2022 Jun 17;11(6):2108-2120. doi: 10.1021/acssynbio.2c00050. Epub 2022 May 12.

Abstract

Engineering regulatory parts for improved performance in genetic programs has played a pivotal role in the development of the synthetic biology cell programming toolbox. Here, we report the development of a novel high-throughput platform for regulatory part prototyping and analysis that leverages the advantages of engineered DNA libraries, cell-free protein synthesis (CFPS), high-throughput emulsion droplet microfluidics, standard flow sorting adapted to screen droplet reactions, and next-generation sequencing (NGS). With this integrated platform, we screened the activity of millions of genetic parts within hours, followed by NGS retrieval of the improved designs. This platform is particularly valuable for engineering regulatory parts of nonmodel organisms, where high-throughput screening methods are not readily available. The platform can be extended to multipart screening of complete genetic programs to optimize yield and stability.

摘要

工程调控元件在提高遗传程序的性能方面发挥了关键作用,是合成生物学细胞编程工具包的重要组成部分。在这里,我们报告了一种新型的调控元件原型设计和分析的高通量平台的开发,该平台利用了工程化 DNA 文库、无细胞蛋白合成 (CFPS)、高通量乳液液滴微流控、适用于筛选液滴反应的标准流式分选以及下一代测序 (NGS) 的优势。通过这个集成平台,我们在数小时内筛选了数百万个遗传元件的活性,然后通过 NGS 检索改进的设计。这个平台在工程非模式生物的调控元件方面特别有价值,因为在这些生物中,高通量筛选方法并不容易获得。该平台可以扩展到完整遗传程序的多部分筛选,以优化产量和稳定性。

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