Skiba Meredith A, Maloney Finn P, Dan Qingyun, Fraley Amy E, Aldrich Courtney C, Smith Janet L, Brown W Clay
University of Michigan, Ann Arbor, MI, United States.
University of Minnesota, Minneapolis, MN, United States.
Methods Enzymol. 2018;604:45-88. doi: 10.1016/bs.mie.2018.01.035. Epub 2018 Mar 16.
The structural diversity and complexity of marine natural products have made them a rich and productive source of new bioactive molecules for drug development. The identification of these new compounds has led to extensive study of the protein constituents of the biosynthetic pathways from the producing microbes. Essential processes in the dissection of biosynthesis have been the elucidation of catalytic functions and the determination of 3D structures for enzymes of the polyketide synthases and nonribosomal peptide synthetases that carry out individual reactions. The size and complexity of these proteins present numerous difficulties in the process of going from gene to structure. Here, we review the problems that may be encountered at the various steps of this process and discuss some of the solutions devised in our and other labs for the cloning, production, purification, and structure solution of complex proteins using Escherichia coli as a heterologous host.
海洋天然产物的结构多样性和复杂性使其成为药物开发中新生物活性分子丰富且高效的来源。这些新化合物的鉴定促使人们对产生这些化合物的微生物生物合成途径中的蛋白质成分进行广泛研究。剖析生物合成过程中的关键步骤包括阐明催化功能以及确定负责各个反应的聚酮合酶和非核糖体肽合成酶的三维结构。这些蛋白质的大小和复杂性给从基因到结构的过程带来了诸多困难。在此,我们综述了该过程各个步骤可能遇到的问题,并讨论了我们实验室和其他实验室为利用大肠杆菌作为异源宿主对复杂蛋白质进行克隆、生产、纯化及结构解析所设计的一些解决方案。