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多酶组装策略。

Strategies for Multienzyme Assemblies.

机构信息

Department of Chemical Engineering, Texas A&M University, College Station, TX, USA.

Department of Chemical and Materials Engineering, University of Nevada, Reno, NV, USA.

出版信息

Methods Mol Biol. 2022;2487:113-131. doi: 10.1007/978-1-0716-2269-8_7.

Abstract

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 co-localize 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.

摘要

蛋白质并非独立存在的实体,必须协调它们的集体行动以达到最佳性能。自然界通过进化发展出了将级联酶反应的功能伙伴共定位的能力,以确保中间产物的有效交换。受这些自然设计的启发,已经创建了合成支架来增强整体生物途径的性能。在本章中,我们描述了几种基于 DNA 和蛋白质的支架方法,用于组装用于各种应用的人工酶级联。我们强调了这些方法的关键优点和缺点,以提供有关如何为不同的级联系统选择适当支架的见解。

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