Department of Chemistry, North Carolina State University, Raleigh, NC, United States.
Department of Chemistry, Carnegie Mellon University, Pittsburgh, PA, United States.
Methods Enzymol. 2024;704:91-111. doi: 10.1016/bs.mie.2024.05.003. Epub 2024 Jun 29.
Cyclopropane and azacyclopropane, also known as aziridine, moieties are found in natural products. These moieties serve as pivotal components that lead to a broad spectrum of biological activities. While diverse strategies involving various classes of enzymes are utilized to catalyze formation of these strained three-membered rings, how non-heme iron and 2-oxoglutarate (Fe/2OG) dependent enzymes enable regio- and stereo-selective C-C and C-N ring closure has only been reported very recently. Herein, we present detailed experimental protocols for mechanistically studying Fe/2OG enzymes that catalyze cyclopropanation and aziridination reactions. These protocols include protein purification, in vitro assays, biophysical spectroscopies, and isotope-tracer experiments. We also report how to use in silico approaches to look for Fe/2OG aziridinases. Furthermore, our current mechanistic understanding of three-membered ring formation is discussed. These results not only shed light on the reaction mechanisms of Fe/2OG enzymes-catalyzed cyclopropanation and aziridination, but also open avenues for expanding the reaction repertoire of the Fe/2OG enzyme superfamily.
环丙烷和氮杂环丙烷,也称为氮丙啶,是天然产物中的重要结构单元。这些结构单元作为关键组成部分,导致了广泛的生物活性。虽然涉及各种酶类的多种策略被用于催化这些张力的三元环的形成,但非血红素铁和 2-氧戊二酸(Fe/2OG)依赖性酶如何实现区域和立体选择性的 C-C 和 C-N 环闭合,直到最近才被报道。本文提供了详细的实验方案,用于研究催化环丙烷化和氮丙啶化反应的 Fe/2OG 酶的机制。这些方案包括蛋白质纯化、体外测定、生物物理光谱学和同位素示踪实验。我们还报告了如何使用计算方法寻找 Fe/2OG 氮丙啶酶。此外,我们还讨论了目前对三元环形成的机制理解。这些结果不仅阐明了 Fe/2OG 酶催化的环丙烷化和氮丙啶化反应的机制,而且为扩展 Fe/2OG 酶超家族的反应谱开辟了途径。