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生物合成超大酶的结构生物学。

The structural biology of biosynthetic megaenzymes.

机构信息

UMR 7365, Ingénierie Moléculaire et Physiopathologie Articulaire (IMoPA), CNRS-Université de Lorraine, Biopôle de l'Université de Lorraine, Campus Biologie Santé, Vandœuvre-lès-Nancy, France.

出版信息

Nat Chem Biol. 2015 Sep;11(9):660-70. doi: 10.1038/nchembio.1883.

Abstract

The modular polyketide synthases (PKSs) and nonribosomal peptide synthetases (NRPSs) are among the largest and most complicated enzymes in nature. In these biosynthetic systems, independently folding protein domains, which are organized into units called 'modules', operate in assembly-line fashion to construct polymeric chains and tailor their functionalities. Products of PKSs and NRPSs include a number of blockbuster medicines, and this has motivated researchers to understand how they operate so that they can be modified by genetic engineering. Beginning in the 1990s, structural biology has provided a number of key insights. The emerging picture is one of remarkable dynamics and conformational programming in which the chemical states of individual catalytic domains are communicated to the others, configuring the modules for the next stage in the biosynthesis. This unexpected level of complexity most likely accounts for the low success rate of empirical genetic engineering experiments and suggests ways forward for productive megaenzyme synthetic biology.

摘要

模块化聚酮合酶 (PKSs) 和非核糖体肽合酶 (NRPSs) 是自然界中最大和最复杂的酶之一。在这些生物合成系统中,独立折叠的蛋白质结构域,它们被组织成称为“模块”的单元,以装配线的方式操作,构建聚合链并调整其功能。PKSs 和 NRPSs 的产物包括许多重磅药物,这激发了研究人员去理解它们的作用机制,以便通过基因工程进行修饰。从 20 世纪 90 年代开始,结构生物学提供了一些关键的见解。新兴的图景是显著的动力学和构象编程,其中单个催化结构域的化学状态被传递给其他结构域,为生物合成的下一个阶段配置模块。这种出乎意料的复杂性很可能是经验性基因工程实验成功率低的原因,并为富有成效的巨型酶合成生物学指明了前进的方向。

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