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线性DNA在无细胞表达系统中的有效应用。

Effective Use of Linear DNA in Cell-Free Expression Systems.

作者信息

McSweeney Megan A, Styczynski Mark P

机构信息

Georgia Institute of Technology, School of Chemical & Biomolecular Engineering, Atlanta, GA, United States.

出版信息

Front Bioeng Biotechnol. 2021 Jul 20;9:715328. doi: 10.3389/fbioe.2021.715328. eCollection 2021.

DOI:10.3389/fbioe.2021.715328
PMID:34354989
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8329657/
Abstract

Cell-free expression systems (CFEs) are cutting-edge research tools used in the investigation of biological phenomena and the engineering of novel biotechnologies. While CFEs have many benefits over protein synthesis, one particularly significant advantage is that CFEs allow for gene expression from both plasmid DNA and linear expression templates (LETs). This is an important and impactful advantage because functional LETs can be efficiently synthesized in a few hours without transformation and cloning, thus expediting genetic circuit prototyping and allowing expression of toxic genes that would be difficult to clone through standard approaches. However, native nucleases present in the crude bacterial lysate (the basis for the most affordable form of CFEs) quickly degrade LETs and limit expression yield. Motivated by the significant benefits of using LETs in lieu of plasmid templates, numerous methods to enhance their stability in lysate-based CFEs have been developed. This review describes approaches to LET stabilization used in CFEs, summarizes the advancements that have come from using LETs with these methods, and identifies future applications and development goals that are likely to be impactful to the field. Collectively, continued improvement of LET-based expression and other linear DNA tools in CFEs will help drive scientific discovery and enable a wide range of applications, from diagnostics to synthetic biology research tools.

摘要

无细胞表达系统(CFEs)是用于研究生物现象和新型生物技术工程的前沿研究工具。虽然CFEs在蛋白质合成方面有许多优势,但一个特别显著的优势是,CFEs允许从质粒DNA和线性表达模板(LETs)进行基因表达。这是一个重要且有影响力的优势,因为功能性LETs可以在几个小时内高效合成,无需转化和克隆,从而加快遗传电路原型设计,并允许表达通过标准方法难以克隆的有毒基因。然而,粗制细菌裂解物(最经济实惠的CFEs形式的基础)中存在的天然核酸酶会迅速降解LETs并限制表达产量。受使用LETs代替质粒模板的显著优势的推动,人们开发了许多方法来提高它们在基于裂解物的CFEs中的稳定性。本综述描述了CFEs中用于LET稳定化的方法,总结了使用这些方法的LETs所取得的进展,并确定了可能对该领域有影响的未来应用和发展目标。总体而言,CFEs中基于LET的表达和其他线性DNA工具的持续改进将有助于推动科学发现,并实现从诊断到合成生物学研究工具等广泛的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75df/8329657/e0950528913b/fbioe-09-715328-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75df/8329657/3a99b88ff1ac/fbioe-09-715328-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75df/8329657/a93986ce895e/fbioe-09-715328-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75df/8329657/e0950528913b/fbioe-09-715328-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75df/8329657/3a99b88ff1ac/fbioe-09-715328-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75df/8329657/a93986ce895e/fbioe-09-715328-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75df/8329657/e0950528913b/fbioe-09-715328-g003.jpg

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