Program in Chemical Biology, University of Michigan, 210 Washtenaw Ave., Ann Arbor, MI, 48109, USA.
Life Sciences Institute, University of Michigan, 210 Washtenaw Ave., Ann Arbor, MI, 48109, USA.
Chembiochem. 2019 May 15;20(10):1231-1241. doi: 10.1002/cbic.201800754. Epub 2019 Mar 27.
Natural product biosynthetic pathways are composed of enzymes that use powerful chemistry to assemble complex molecules. Small molecule neurotoxins are examples of natural products with intricate scaffolds which often have high affinities for their biological targets. The focus of this Minireview is small molecule neurotoxins targeting voltage-gated sodium channels (VGSCs) and the state of knowledge on their associated biosynthetic pathways. There are three small molecule neurotoxin receptor sites on VGSCs associated with three different classes of molecules: guanidinium toxins, alkaloid toxins, and ladder polyethers. Each of these types of toxins have unique structural features which are assembled by biosynthetic enzymes and the extent of information known about these enzymes varies among each class. The biosynthetic enzymes involved in the formation of these toxins have the potential to become useful tools in the efficient synthesis of VGSC probes.
天然产物生物合成途径由利用强大化学方法组装复杂分子的酶组成。小分子神经毒素是具有复杂支架的天然产物的例子,这些支架通常对其生物靶标具有高亲和力。本综述的重点是针对电压门控钠离子通道 (VGSC) 的小分子神经毒素,以及与其相关的生物合成途径的知识状况。VGSC 上有三个与三种不同类型分子相关的小分子神经毒素受体位点:胍毒素、生物碱毒素和梯状聚醚。这些类型的毒素中的每一种都具有独特的结构特征,这些特征由生物合成酶组装,并且每种类型的酶的相关信息程度也不同。参与这些毒素形成的生物合成酶有可能成为高效合成 VGSC 探针的有用工具。