Sun Qing, Tsai Shen-Long, Chen Wilfred
Department of Chemical Engineering, Texas A&M University, College Station, TX, United States.
Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei City, Taiwan.
Methods Enzymol. 2019;617:363-383. doi: 10.1016/bs.mie.2018.12.007. Epub 2019 Jan 25.
Proteins are not designed to be standalone entities and must coordinate their collective action for optimum performance. Nature has developed through evolution the ability to colocalize the functional partners of a cascade enzymatic reaction in order to ensure efficient exchange of intermediates. Inspired by these natural designs, synthetic scaffolds have been created to enhance the overall biological pathway performance. In this chapter, we describe several DNA- and protein-based scaffold approaches to assemble artificial enzyme cascades for a wide range of applications. We highlight the key benefits and drawbacks of these approaches to provide insights on how to choose the appropriate scaffold for different cascade systems.
蛋白质并非设计为独立存在的实体,它们必须协调其集体行动以实现最佳性能。通过进化,自然界已发展出将级联酶促反应的功能伙伴共定位的能力,以确保中间体的高效交换。受这些自然设计的启发,人们创建了合成支架以增强整体生物途径性能。在本章中,我们描述了几种基于DNA和蛋白质的支架方法,用于组装适用于广泛应用的人工酶级联反应。我们强调了这些方法的主要优点和缺点,以提供有关如何为不同级联系统选择合适支架的见解。