非核糖体肽
计算生物学
鉴定(生物学)
肽
环肽
达托霉素
生物
蛋白质组学
质谱法
基因组
DNA测序
组合化学
化学
遗传学
生物化学
基因
生物合成
细菌
色谱法
万古霉素
植物
金黄色葡萄球菌
作者
Hosein Mohimani,Wei-Ting Liu,Roland D. Kersten,Bradley S. Moore,Pieter C. Dorrestein,Pavel A. Pevzner
摘要
Nonribosomal peptides (NRPs) such as vancomycin and daptomycin are among the most effective antibiotics. While NRPs are biomedically important, the computational techniques for sequencing these peptides are still in their infancy. The recent emergence of mass spectrometry techniques for NRP analysis (capable of sequencing an NRP from small amounts of nonpurified material) revealed an enormous diversity of NRPs. However, as many NRPs have nonlinear structure (e.g., cyclic or branched-cyclic peptides), the standard de novo sequencing tools (developed for linear peptides) are not applicable to NRP analysis. Here, we introduce the first NRP identification algorithm, NRPquest, that performs mutation-tolerant and modification-tolerant searches of spectral data sets against a database of putative NRPs. In contrast to previous studies aimed at NRP discovery (that usually report very few NRPs), NRPquest revealed nearly a hundred NRPs (including unknown variants of previously known peptides) in a single study. This result indicates that NRPquest can potentially make MS-based NRP identification as robust as the identification of linear peptides in traditional proteomics.
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