Zuo Yilang, Gong Shilin, Zhang Li, Zhou Jie, Wu Jian-Lin, Li Na
State Key Laboratory of Quality Research in Chinese Medicine, Macau Institute for Applied Research in Medicine and Health, Macau University of Science and Technology, Taipa, Macau 999078, China.
Metabolites. 2024 Aug 23;14(9):467. doi: 10.3390/metabo14090467.
() is widely recognized as a probiotic that produces prebiotics. However, studies on bioactive peptides or amino acid (AA) derivatives produced by are still lacking, whereas many bioactive peptides and AA derivatives have been found in other species. In addition, rapid identification of peptides is challenged by the large amount of data and is limited by the coverage of protein databases. In this study, we performed a rapid and thorough profile of peptides in incorporating Global Natural Products Social Molecular Networking (GNPS) platform database searching, de novo sequencing, and deep mining, based on feature-based molecular networking (FBMN). According to FBMN, it was found that peptides containing identical or similar AA compositions were grouped into the same clusters, especially cyclic dipeptides (CDPs). Therefore, the grouping characteristics of clusters, differences in precursor ions, and characteristic fragment ions were utilized for the mining of deeply unknown compounds. Through this strategy, a total of 192 compounds, including 184 peptides, were rapidly identified. Among them, 53 CDPs, including four novel ones, were found for the first time in . Then, one of the novel CDPs, cyclo(5-OMe-Glu-4-OH-Pro), was isolated and characterized, which was consistent with the identification results. Moreover, some of the identified peptides exhibited considerable interactions with seven anti-inflammatory-related target proteins through molecular docking. According to the binding energies of peptides with different AA consistencies, it was considered that the existence of unnatural AAs in CDPs might contribute to their anti-inflammatory activity. These results provide a valuable strategy for the rapid identification of peptides, including CDPs. This study also reveals the substance basis for the potential anti-inflammatory effects exerted by .
(某物质)被广泛认为是一种能产生益生元的益生菌。然而,关于该物质产生的生物活性肽或氨基酸(AA)衍生物的研究仍然缺乏,而在其他(相关)物种中已发现许多生物活性肽和AA衍生物。此外,肽的快速鉴定面临大量数据的挑战,并且受到蛋白质数据库覆盖范围的限制。在本研究中,我们基于基于特征的分子网络(FBMN),结合全球天然产物社会分子网络(GNPS)平台数据库搜索、从头测序和深度挖掘,对(该物质中的)肽进行了快速而全面的分析。根据FBMN,发现含有相同或相似AA组成的肽被分组到同一簇中,尤其是环二肽(CDP)。因此,利用簇的分组特征、前体离子的差异和特征性碎片离子来挖掘深度未知的化合物。通过这种策略,总共快速鉴定出192种化合物,包括184种肽。其中,首次在(该物质中)发现了53种CDP,包括4种新的CDP。然后,分离并鉴定了其中一种新的CDP,环(5 - OMe - Glu - 4 - OH - Pro),这与鉴定结果一致。此外,一些鉴定出的肽通过分子对接与七种抗炎相关靶蛋白表现出相当大的相互作用。根据具有不同AA组成的肽的结合能,认为CDP中不自然AA的存在可能有助于它们的抗炎活性。这些结果为包括CDP在内的肽的快速鉴定提供了有价值的策略。本研究还揭示了(该物质)发挥潜在抗炎作用的物质基础。