Nelson Samantha, Parkinson Elizabeth I
Borch Department of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, Indiana 47906, USA.
James Tarpo Jr. and Margaret Tarpo Department of Chemistry, Purdue University, West Lafayette, Indiana 47906, USA.
Nat Prod Rep. 2025 Jan 22;42(1):50-66. doi: 10.1039/d4np00043a.
Covering: 2016 to 2024Natural products, particularly cyclic peptides, are a promising source of bioactive compounds. Nonribosomal peptide synthetases (NRPSs) play a key role in biosynthesizing these compounds, which include antibiotic and anticancer agents, immunosuppressants, and others. Traditional methods of discovering natural products have limitations including cryptic biosynthetic gene clusters (BGCs), low titers, and currently unculturable organisms. This has prompted the exploration of alternative approaches. Synthetic-bioinformatic natural products (-BNPs) are one such alternative that utilizes bioinformatics techniques to predict nonribosomal peptides (NRPs) followed by chemical synthesis of the predicted peptides. This approach has shown promise, resulting in the discovery of a variety of bioactive compounds including peptides with antibacterial, antifungal, anticancer, and proteasome-stimulating activities. Despite the success of this approach, challenges remain especially in the accurate prediction of fatty acid incorporation, tailoring enzyme modifications, and peptide release mechanisms. Further work in these areas will enable the discovery of many bioactive peptides that are currently inaccessible.
2016年至2024年
天然产物,尤其是环肽,是生物活性化合物的一个有前景的来源。非核糖体肽合成酶(NRPSs)在这些化合物的生物合成中起关键作用,这些化合物包括抗生素、抗癌剂、免疫抑制剂等。传统的天然产物发现方法存在局限性,包括隐蔽的生物合成基因簇(BGCs)、低产量以及目前无法培养的生物体。这促使人们探索替代方法。合成生物信息学天然产物(-BNPs)就是这样一种替代方法,它利用生物信息学技术预测非核糖体肽(NRPs),然后对预测出的肽进行化学合成。这种方法已显示出前景,导致发现了多种生物活性化合物,包括具有抗菌、抗真菌、抗癌和蛋白酶体刺激活性的肽。尽管这种方法取得了成功,但挑战仍然存在,尤其是在脂肪酸掺入、修饰酶修饰和肽释放机制的准确预测方面。在这些领域的进一步研究将有助于发现许多目前难以获得的生物活性肽。