Rochester Institute of Technology, Thomas H. Gosnell School of Life Sciences, Rochester, New York, USA.
Biomolecular Interaction Centre and School of Biological Sciences, University of Canterbury, Christchurch, New Zealand; Bio21 Molecular Science and Biotechnology Institute, Department of Biochemistry and Molecular Biology, University of Melbourne, Parkville, Victoria, Australia.
J Biol Chem. 2021 Jan-Jun;296:100438. doi: 10.1016/j.jbc.2021.100438. Epub 2021 Feb 19.
For millennia, humanity has relied on plants for its medicines, and modern pharmacology continues to reexamine and mine plant metabolites for novel compounds and to guide improvements in biological activity, bioavailability, and chemical stability. The critical problem of antibiotic resistance and increasing exposure to viral and parasitic diseases has spurred renewed interest into drug treatments for infectious diseases. In this context, an urgent revival of natural product discovery is globally underway with special attention directed toward the numerous and chemically diverse plant defensive compounds such as phytoalexins and phytoanticipins that combat herbivores, microbial pathogens, or competing plants. Moreover, advancements in "omics," chemistry, and heterologous expression systems have facilitated the purification and characterization of plant metabolites and the identification of possible therapeutic targets. In this review, we describe several important amino acid-derived classes of plant defensive compounds, including antimicrobial peptides (e.g., defensins, thionins, and knottins), alkaloids, nonproteogenic amino acids, and phenylpropanoids as potential drug leads, examining their mechanisms of action, therapeutic targets, and structure-function relationships. Given their potent antibacterial, antifungal, antiparasitic, and antiviral properties, which can be superior to existing drugs, phytoalexins and phytoanticipins are an excellent resource to facilitate the rational design and development of antimicrobial drugs.
几千年来,人类一直依赖植物来获取药物,现代药理学继续重新审视和挖掘植物代谢产物中的新型化合物,以指导提高生物活性、生物利用度和化学稳定性。抗生素耐药性的关键问题以及越来越多的病毒和寄生虫疾病的暴露,促使人们重新关注传染病的药物治疗。在这种情况下,全球范围内正在紧急复兴天然产物的发现,特别关注对抗草食动物、微生物病原体或竞争植物的众多化学多样的植物防御化合物,如植物抗毒素和植物防御素。此外,“组学”、化学和异源表达系统的进步促进了植物代谢产物的纯化和表征,以及可能的治疗靶点的鉴定。在这篇综述中,我们描述了几种重要的氨基酸衍生类植物防御化合物,包括抗菌肽(如防御素、硫素和 knottins)、生物碱、非蛋白氨基酸和苯丙烷类化合物,它们可能是潜在的药物先导化合物,研究了它们的作用机制、治疗靶点和结构-功能关系。鉴于其强大的抗菌、抗真菌、抗寄生虫和抗病毒特性,其效果优于现有药物,植物抗毒素和植物防御素是促进抗菌药物合理设计和开发的极好资源。