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NRPquest: Coupling Mass Spectrometry and Genome Mining for Nonribosomal Peptide Discovery

[Image: see text] 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 technique...

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Autores principales: Mohimani, Hosein, Liu, Wei-Ting, Kersten, Roland D., Moore, Bradley S., Dorrestein, Pieter C., Pevzner, Pavel A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society and American Society of Pharmacognosy 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143176/
https://www.ncbi.nlm.nih.gov/pubmed/25116163
http://dx.doi.org/10.1021/np500370c
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author Mohimani, Hosein
Liu, Wei-Ting
Kersten, Roland D.
Moore, Bradley S.
Dorrestein, Pieter C.
Pevzner, Pavel A.
author_facet Mohimani, Hosein
Liu, Wei-Ting
Kersten, Roland D.
Moore, Bradley S.
Dorrestein, Pieter C.
Pevzner, Pavel A.
author_sort Mohimani, Hosein
collection PubMed
description [Image: see text] 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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spelling pubmed-41431762015-08-12 NRPquest: Coupling Mass Spectrometry and Genome Mining for Nonribosomal Peptide Discovery Mohimani, Hosein Liu, Wei-Ting Kersten, Roland D. Moore, Bradley S. Dorrestein, Pieter C. Pevzner, Pavel A. J Nat Prod [Image: see text] 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. American Chemical Society and American Society of Pharmacognosy 2014-08-12 2014-08-22 /pmc/articles/PMC4143176/ /pubmed/25116163 http://dx.doi.org/10.1021/np500370c Text en Copyright © 2014 American Chemical Society and American Society of Pharmacognosy Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html)
spellingShingle Mohimani, Hosein
Liu, Wei-Ting
Kersten, Roland D.
Moore, Bradley S.
Dorrestein, Pieter C.
Pevzner, Pavel A.
NRPquest: Coupling Mass Spectrometry and Genome Mining for Nonribosomal Peptide Discovery
title NRPquest: Coupling Mass Spectrometry and Genome Mining for Nonribosomal Peptide Discovery
title_full NRPquest: Coupling Mass Spectrometry and Genome Mining for Nonribosomal Peptide Discovery
title_fullStr NRPquest: Coupling Mass Spectrometry and Genome Mining for Nonribosomal Peptide Discovery
title_full_unstemmed NRPquest: Coupling Mass Spectrometry and Genome Mining for Nonribosomal Peptide Discovery
title_short NRPquest: Coupling Mass Spectrometry and Genome Mining for Nonribosomal Peptide Discovery
title_sort nrpquest: coupling mass spectrometry and genome mining for nonribosomal peptide discovery
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143176/
https://www.ncbi.nlm.nih.gov/pubmed/25116163
http://dx.doi.org/10.1021/np500370c
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