NRPquest: Coupling Mass Spectrometry and Genome Mining for Nonribosomal Peptide Discovery
Author(s) -
Hosein Mohimani,
Wei-Ting Liu,
Roland D. Kersten,
Bradley S. Moore,
Pieter C. Dorrestein,
Pavel A. Pevzner
Publication year - 2014
Publication title -
journal of natural products
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.976
H-Index - 139
eISSN - 1520-6025
pISSN - 0163-3864
DOI - 10.1021/np500370c
Subject(s) - nonribosomal peptide , computational biology , identification (biology) , peptide , cyclic peptide , daptomycin , biology , proteomics , mass spectrometry , genome , dna sequencing , combinatorial chemistry , chemistry , genetics , biochemistry , gene , biosynthesis , bacteria , chromatography , botany , vancomycin , staphylococcus aureus
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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