Evidence map›Paper›PMID 31659720›Full record

ArticleJournal of the American Society for Mass Spectrometry2019

Kendrick Mass Defect Approach Combined to NORINE Database for Molecular Formula Assignment of Nonribosomal Peptides.

Mickaël Chevalier, Emma Ricart, Emeline Hanozin, Maude Pupin, Philippe Jacques, Nicolas Smargiasso, Edwin De Pauw, Frédérique Lisacek, Valérie Leclère, Christophe Flahaut

Abstract read
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In one paragraph

Article in Journal of the American Society for Mass Spectrometry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Molecules (Basel, Switzerland) · 2019
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Mickaël ChevalierUniv. Lille, INRA, ISA, Univ. Artois, Univ. Littoral Côte d'Opale, EA 7394-Institut Charles Viollette (ICV), F-59000, Lille, France.
Emma RicartProteome informatics Group, SIB Swiss Institute of Bioinformatics (SIB), and Computer Science Department, University of Geneva, Geneva, Switzerland.
Emeline HanozinMass Spectrometry Laboratory, Molecular Systems - MolSys Research Unit, University of Liège, Liège, Belgium.
Maude PupinUniv. Lille, CNRS, Centrale Lille, UMR 9189 - CRIStAL - Centre de Recherche en Informatique Signal et Automatique de Lille, F-59000, Lille, France.
Philippe JacquesTERRA Research Centre, Microbial Processes and Interactions (MiPI), Gembloux Agro-Bio Tech University of Liège, B-5030, Gembloux, Belgium.
Nicolas SmargiassoMass Spectrometry Laboratory, Molecular Systems - MolSys Research Unit, University of Liège, Liège, Belgium.
Edwin De PauwMass Spectrometry Laboratory, Molecular Systems - MolSys Research Unit, University of Liège, Liège, Belgium.
Frédérique LisacekProteome informatics Group, SIB Swiss Institute of Bioinformatics (SIB), and Computer Science Department, University of Geneva, Geneva, Switzerland.
Valérie LeclèreUniv. Lille, INRA, ISA, Univ. Artois, Univ. Littoral Côte d'Opale, EA 7394-Institut Charles Viollette (ICV), F-59000, Lille, France.
Christophe FlahautUniv. Lille, INRA, ISA, Univ. Artois, Univ. Littoral Côte d'Opale, EA 7394-Institut Charles Viollette (ICV), F-59000, Lille, France. christophe.flahaut@univ-artois.fr.ORCID http://orcid.org/0000-0002-2603-962X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The identification of known (dereplication) or unknown nonribosomal peptides (NRPs) produced by microorganisms is a time consuming, expensive, and challenging task where mass spectrometry and nuclear magnetic resonance play a key role. The first step of the identification process always involves the establishment of a molecular formula. Unfortunately, the number of potential molecular formulae increases significantly with higher molecular masses and the lower precision of their measurements. In the present article, we demonstrate that molecular formula assignment can be achieved by a combined approach using the regular Kendrick mass defect (RKMD) and NORINE, the reference curated database of NRPs. We observed that irrespective of the molecular formula, the addition and subtraction of a given atom or atom group always leads to the same RKMD variation and nominal Kendrick mass (NKM). Graphically, these variations translated into a vector mesh can be used to connect an unknown molecule to a known NRP of the NORINE database and establish its molecular formula. We explain and illustrate this concept through the high-resolution mass spectrometry analysis of a commercially available mixture composed of four surfactins. The Kendrick approach enriched with the NORINE database content is a fast, useful, and easy-to-use tool for molecular mass assignment of known and unknown NRP structures.

Indexed as

Databases, ProteinLipopeptidesMolecular WeightPeptide Biosynthesis, Nucleic Acid-IndependentPeptidesPeptides, CyclicProtonsSoftwareSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationLipopeptidesPeptidesPeptides, CyclicProtonssurfactin peptideKendrick mapMass defectMolecular formulaNonribosomal peptidesNORINE

Identifiers

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.