Fast and facile preparation of nanostructured silicon surfaces for laser desorption/ionization mass spectrometry of small compounds.


Journal

Rapid communications in mass spectrometry : RCM
ISSN: 1097-0231
Titre abrégé: Rapid Commun Mass Spectrom
Pays: England
ID NLM: 8802365

Informations de publication

Date de publication:
May 2019
Historique:
received: 30 04 2018
revised: 13 07 2018
accepted: 16 07 2018
pubmed: 27 7 2018
medline: 31 12 2019
entrez: 27 7 2018
Statut: ppublish

Résumé

Many important biological processes rely on specific biomarkers (such as metabolites, drugs, proteins or peptides, carbohydrates, lipids, ...) that need to be monitored in various fluids (blood, plasma, urine, cell cultures, tissue homogenates, …). Although mass spectrometry (MS) hyphenated to liquid chromatography (LC) is widely accepted as a 'gold-standard' method for identifying such synthetic chemicals or biological products, their robust fast sensitive detection from complex matrices still constitutes a highly challenging matter. In order to circumvent the constraints intrinsic to LC/MS technology in terms of prior sample treatment, analysis time and overall method development to optimize ionization efficiency affecting the detection threshold, we investigated laser desorption/ionization mass spectrometry (LDI-MS) by directly depositing the sample under study onto cheap inert nanostructures made of silicon to perform straightforward sensitive and rapid screening of targeted low mass biomarkers on a conventional MALDI platform. The investigated silicon nanostructures were found to act as very efficient ion-promoting surfaces exhibiting high performance for the detection of different classes of organic compounds, including glutathione, glucose, peptides and antibiotics. Achieving such broad detection was compulsory to develop a SALDI-MS-based pre-screening tool. The key contribution of the described analytical strategy consists of designing inert surfaces that are fast (minute preparation) and cheap to produce, easy to handle and able to detect small organic compounds in matrix-free LDI-MS prerequisite for biomarkers pre-screening from body fluids without the recourse of any separation step.

Identifiants

pubmed: 30048019
doi: 10.1002/rcm.8245
doi:

Substances chimiques

Anti-Bacterial Agents 0
Biomarkers 0
Peptides 0
Glutathione GAN16C9B8O
Silicon Z4152N8IUI

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

66-74

Subventions

Organisme : Centre National de la Recherche Scientifique
Organisme : Université Lille 1 - Sciences et Technologies
Organisme : Ministry of Higher Education, Scientific Research and Technology of Tunisia
Organisme : French RENATECH network (French national nanofabrication platform)
Organisme : Hauts-de-France region
Organisme : Centre National de la Recherche Scientifique (CNRS)

Informations de copyright

© 2018 John Wiley & Sons, Ltd.

Références

Nat Methods. 2004 Oct;1(1):39-45
pubmed: 15782151
BMC Bioinformatics. 2006 Apr 28;7:234
pubmed: 16646969
BMC Bioinformatics. 2007 Mar 27;8:105
pubmed: 17389044
Anal Chem. 2007 Nov 15;79(22):8631-8
pubmed: 17927139
Anal Chem. 2009 May 15;81(10):3919-32
pubmed: 19309105
Methods Mol Biol. 2010;658:217-31
pubmed: 20839107
Anal Chem. 2010 Nov 1;82(21):8789-93
pubmed: 20945833
J Biol Chem. 2011 Jul 22;286(29):25435-42
pubmed: 21632543
Mol Cell Proteomics. 2012 Jun;11(6):O111.016717
pubmed: 22261725
Anal Chem. 2014 Feb 18;86(4):2107-16
pubmed: 24446877
Anal Chem. 2015 Oct 6;87(19):9838-45
pubmed: 26327437
J Cheminform. 2016 Jan 29;8:3
pubmed: 26834843
Bioinformatics. 2017 Jul 15;33(14):2235-2237
pubmed: 28334295
Anal Chem. 2017 Jun 20;89(12):6384-6391
pubmed: 28528542
Anal Chem. 2017 Sep 5;89(17):9048-9055
pubmed: 28763190
J Chromatogr A. 2017 Dec 1;1526:1-12
pubmed: 29074071
Curr Opin Chem Biol. 2018 Feb;42:9-15
pubmed: 29107931
Curr Opin Chem Biol. 2018 Feb;42:60-66
pubmed: 29161611
Rapid Commun Mass Spectrom. 2019 Feb 22;:null
pubmed: 30801790

Auteurs

Abderrahmane Hamdi (A)

Univ. Lille, CNRS, Centrale Lille, ISEN, Univ. Valenciennes, IEMN, UMR CNRS 8520, Avenue Poincaré, BP 60069, 59652, Villeneuve d'Ascq, France.
Laboratory of Semi-conductors, Nano-structures and Advanced Technologies, Research and Technology Centre of Energy, Borj-Cedria Science and Technology Park, BP 95, 2050, Hammam-Lif, Tunisia.
Faculty of Science of Bizerte, University of Carthage, 7021, Zarzouna, Tunisia.

Christine Enjalbal (C)

Univ. Montpellier, Institut des Biomolécules Max Mousseron, Place Eugène Bataillon, 34095, Montpellier, France.

Hervé Drobecq (H)

Institut de biologie de Lille, UMR CNRS 8160, 59000, Lille, France.

Rabah Boukherroub (R)

Univ. Lille, CNRS, Centrale Lille, ISEN, Univ. Valenciennes, IEMN, UMR CNRS 8520, Avenue Poincaré, BP 60069, 59652, Villeneuve d'Ascq, France.

Oleg Melnyk (O)

Institut de biologie de Lille, UMR CNRS 8160, 59000, Lille, France.

Hatem Ezzaouia (H)

Laboratory of Semi-conductors, Nano-structures and Advanced Technologies, Research and Technology Centre of Energy, Borj-Cedria Science and Technology Park, BP 95, 2050, Hammam-Lif, Tunisia.

Yannick Coffinier (Y)

Univ. Lille, CNRS, Centrale Lille, ISEN, Univ. Valenciennes, IEMN, UMR CNRS 8520, Avenue Poincaré, BP 60069, 59652, Villeneuve d'Ascq, France.

Articles similaires

Vancomycin-associated DRESS demonstrates delay in AST abnormalities.

Ahmed Hussein, Kateri L Schoettinger, Jourdan Hydol-Smith et al.
1.00
Humans Drug Hypersensitivity Syndrome Vancomycin Female Male
C-Reactive Protein Humans Biomarkers Inflammation
Humans Arthroplasty, Replacement, Elbow Prosthesis-Related Infections Debridement Anti-Bacterial Agents
Vancomycin Polyesters Anti-Bacterial Agents Models, Theoretical Drug Liberation

Classifications MeSH