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工程化蛋白质机器:合成生物学的新兴工具。

Engineered Protein Machines: Emergent Tools for Synthetic Biology.

机构信息

School of Chemical and Biomolecular Engineering, Cornell University, Ithaca, NY 14853, USA.

School of Chemical and Biomolecular Engineering, Cornell University, Ithaca, NY 14853, USA.

出版信息

Cell Chem Biol. 2016 Jan 21;23(1):45-56. doi: 10.1016/j.chembiol.2015.12.004.

Abstract

Nature has evolved an array of intricate protein assemblies that work together to perform the chemistry that maintains life. These protein machines function with exquisite specificity and coordination to accomplish their tasks, from DNA and RNA synthesis to protein folding and post-translational modifications. Despite their complexity, synthetic biologists have succeeded in redesigning many aspects of these molecular machines. For example, natural DNA polymerases have now been engineered to catalyze the synthesis of alternative genetic polymers called XNAs, orthogonal RNA polymerases and ribosomes have been engineered to enable the construction of genetic logic gates, and protein biogenesis machinery such as chaperonins and protein translocons have been repurposed to improve folding and expression of recombinant proteins. In this Review, we highlight the progress made in understanding, engineering, and repurposing bacterial protein machines for use in synthetic biology and biotechnology.

摘要

自然界进化出了一系列复杂的蛋白质组装体,它们协同工作,执行维持生命的化学反应。这些蛋白质机器具有极高的特异性和协调性,能够完成从 DNA 和 RNA 合成到蛋白质折叠和翻译后修饰等各种任务。尽管它们很复杂,但合成生物学家已经成功地重新设计了这些分子机器的许多方面。例如,天然 DNA 聚合酶现已被工程改造为催化合成称为 XNAs 的替代遗传聚合物,正交 RNA 聚合酶和核糖体已被工程改造为能够构建遗传逻辑门,伴侣蛋白和蛋白转位器等蛋白质生物发生机制已被重新用于提高重组蛋白的折叠和表达。在这篇综述中,我们强调了在理解、工程改造和重新利用细菌蛋白质机器以用于合成生物学和生物技术方面所取得的进展。

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