Interdisciplinary Biological Sciences Program, Northwestern University, Evanston, IL 60208, USA.
Department of Chemical and Biological Engineering, Northwestern University, Evanston, IL 60208, USA.
Nucleic Acids Res. 2020 Mar 18;48(5):2777-2789. doi: 10.1093/nar/gkaa001.
The synthetic capability of the Escherichia coli ribosome has attracted efforts to repurpose it for novel functions, such as the synthesis of polymers containing non-natural building blocks. However, efforts to repurpose ribosomes are limited by the lack of complete peptidyl transferase center (PTC) active site mutational analyses to inform design. To address this limitation, we leverage an in vitro ribosome synthesis platform to build and test every possible single nucleotide mutation within the PTC-ring, A-loop and P-loop, 180 total point mutations. These mutant ribosomes were characterized by assessing bulk protein synthesis kinetics, readthrough, assembly, and structure mapping. Despite the highly-conserved nature of the PTC, we found that >85% of the PTC nucleotides possess mutational flexibility. Our work represents a comprehensive single-point mutant characterization and mapping of the 70S ribosome's active site. We anticipate that it will facilitate structure-function relationships within the ribosome and make possible new synthetic biology applications.
大肠杆菌核糖体的合成能力引起了人们的关注,希望将其重新用于新型功能,例如合成含有非天然结构单元的聚合物。然而,重新利用核糖体的努力受到缺乏完整肽基转移酶中心(PTC)活性位点突变分析的限制,无法为设计提供信息。为了解决这个限制,我们利用体外核糖体合成平台构建并测试了 PTC 环、A 环和 P 环内的每一个可能的单核苷酸突变,总共 180 个点突变。通过评估批量蛋白质合成动力学、通读、组装和结构映射来表征这些突变核糖体。尽管 PTC 具有高度保守性,但我们发现 PTC 的超过 85%的核苷酸具有突变灵活性。我们的工作代表了对 70S 核糖体活性位点的全面单点突变特征和映射。我们预计,这将促进核糖体内部的结构-功能关系,并为新的合成生物学应用提供可能。