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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society and American
Society of Pharmacognosy
2014
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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. |
format | Online Article Text |
id | pubmed-4143176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society and American
Society of Pharmacognosy |
record_format | MEDLINE/PubMed |
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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