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改进的无细胞RNA和蛋白质合成系统。

Improved cell-free RNA and protein synthesis system.

作者信息

Li Jun, Gu Liangcai, Aach John, Church George M

机构信息

Department of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America.

出版信息

PLoS One. 2014 Sep 2;9(9):e106232. doi: 10.1371/journal.pone.0106232. eCollection 2014.

Abstract

Cell-free RNA and protein synthesis (CFPS) is becoming increasingly used for protein production as yields increase and costs decrease. Advances in reconstituted CFPS systems such as the Protein synthesis Using Recombinant Elements (PURE) system offer new opportunities to tailor the reactions for specialized applications including in vitro protein evolution, protein microarrays, isotopic labeling, and incorporating unnatural amino acids. In this study, using firefly luciferase synthesis as a reporter system, we improved PURE system productivity up to 5 fold by adding or adjusting a variety of factors that affect transcription and translation, including Elongation factors (EF-Ts, EF-Tu, EF-G, and EF4), ribosome recycling factor (RRF), release factors (RF1, RF2, RF3), chaperones (GroEL/ES), BSA and tRNAs. The work provides a more efficient defined in vitro transcription and translation system and a deeper understanding of the factors that limit the whole system efficiency.

摘要

无细胞RNA和蛋白质合成(CFPS)随着产量增加和成本降低,在蛋白质生产中的应用越来越广泛。重组CFPS系统(如使用重组元件的蛋白质合成(PURE)系统)的进展为针对特殊应用定制反应提供了新机会,这些特殊应用包括体外蛋白质进化、蛋白质微阵列、同位素标记以及掺入非天然氨基酸。在本研究中,我们以萤火虫荧光素酶合成作为报告系统,通过添加或调整多种影响转录和翻译的因素,包括延伸因子(EF-Ts、EF-Tu、EF-G和EF4)、核糖体循环因子(RRF)、释放因子(RF1、RF2、RF3)、伴侣蛋白(GroEL/ES)、牛血清白蛋白(BSA)和转运RNA(tRNA),将PURE系统的生产力提高了5倍。这项工作提供了一个更高效的确定的体外转录和翻译系统,并更深入地了解了限制整个系统效率的因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91b7/4152126/f493be3d5d07/pone.0106232.g001.jpg

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