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在批量和细胞大小液滴中的哺乳动物无细胞表达中同时监测转录和翻译。

Simultaneous monitoring of transcription and translation in mammalian cell-free expression in bulk and in cell-sized droplets.

作者信息

Wang Shue, Majumder Sagardip, Emery Nicholas J, Liu Allen P

机构信息

Department of Mechanical Engineering, University of Michigan, Ann Arbor, MI, USA.

Department of Biomedical Engineering, Boston University, Boston, MA, USA.

出版信息

Synth Biol (Oxf). 2018;3(1):ysy005. doi: 10.1093/synbio/ysy005. Epub 2018 May 21.

Abstract

Transcription and translation are two critical processes during eukaryotic gene expression that regulate cellular activities. The development of mammalian cell-free expression (CFE) systems provides a platform for studying these two critical processes for bottom-up synthetic biology applications such as construction of an artificial cell. Moreover, real-time monitoring of the dynamics of synthesized mRNA and protein is key to characterize and optimize gene circuits before implementing in living cells or in artificial cells. However, there are few tools for measurement of mRNA and protein dynamics in mammalian CFE systems. Here, we developed a locked nucleic acid (LNA) probe for monitoring transcription in a HeLa-based CFE system in real-time. By using this LNA probe in conjunction with a fluorescent reporter protein, we were able to simultaneously monitor mRNA and protein dynamics in bulk reactions and cell-sized single-emulsion droplets. We found rapid production of mRNA transcripts that decreased over time as protein production ensued in bulk reactions. Our results also showed that transcription in cell-sized droplets has different dynamics compared to the transcription in bulk reactions. The use of this LNA probe in conjunction with fluorescent proteins in HeLa-based mammalian CFE system provides a versatile platform for studying mRNA dynamics for bottom-up synthetic biology applications.

摘要

转录和翻译是真核基因表达过程中调控细胞活动的两个关键过程。无细胞表达(CFE)系统的发展为自下而上的合成生物学应用(如构建人工细胞)研究这两个关键过程提供了一个平台。此外,在活细胞或人工细胞中实施之前,对合成的mRNA和蛋白质动态进行实时监测是表征和优化基因回路的关键。然而,在哺乳动物CFE系统中,用于测量mRNA和蛋白质动态的工具很少。在这里,我们开发了一种锁核酸(LNA)探针,用于实时监测基于HeLa的CFE系统中的转录。通过将这种LNA探针与荧光报告蛋白结合使用,我们能够在大量反应和细胞大小的单乳液液滴中同时监测mRNA和蛋白质的动态。我们发现在大量反应中,随着蛋白质的产生,mRNA转录本迅速产生并随时间减少。我们的结果还表明,与大量反应中的转录相比,细胞大小液滴中的转录具有不同的动态。在基于HeLa的哺乳动物CFE系统中,将这种LNA探针与荧光蛋白结合使用,为自下而上的合成生物学应用研究mRNA动态提供了一个通用平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39d5/7445775/da5dde9d14f7/ysy005f1.jpg

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