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Enhancing data acquisition for the analysis of complex organic matter in direct-infusion Orbitrap mass spectrometry using micro-scans.
Wolters, Cédric; Flandinet, Laurène; He, Chao; Isa, Junko; Orthous-Daunay, François-Régis; Thissen, Roland; Hörst, Sarah; Vuitton, Véronique.
Afiliación
  • Wolters C; Univ. Grenoble Alpes, CNRS, IPAG, Grenoble, 38000, France.
  • Flandinet L; Univ. Grenoble Alpes, CNRS, IPAG, Grenoble, 38000, France.
  • He C; Department of Earth and Planetary Sciences, Johns Hopkins University, Baltimore, MD, USA.
  • Isa J; Univ. Grenoble Alpes, CNRS, IPAG, Grenoble, 38000, France.
  • Orthous-Daunay FR; Univ. Grenoble Alpes, CNRS, IPAG, Grenoble, 38000, France.
  • Thissen R; Université Paris-Saclay, CNRS, Institut de Chimie Physique UMR8000, Orsay, 91405, France.
  • Hörst S; Department of Earth and Planetary Sciences, Johns Hopkins University, Baltimore, MD, USA.
  • Vuitton V; Univ. Grenoble Alpes, CNRS, IPAG, Grenoble, 38000, France.
Rapid Commun Mass Spectrom ; 34(15): e8818, 2020 Aug 15.
Article en En | MEDLINE | ID: mdl-32342561
ABSTRACT
RATIONALE Acquisition quality in analytical science is key to obtaining optimal data from a sample. In very high-resolution mass spectrometry, quality is driven by the optimization of multiple parameters, including the use of scans and micro-scans (or transients) for performing a Fourier transformation.

METHODS:

Thirty-nine mass spectra of a single synthesized complex sample were acquired using various numbers of scans and micro-scans determined through a simple experimental design. An electrospray ionization source coupled with an LTQ Orbitrap XL™ mass spectrometer was used, and acquisition was performed using a single mass range. All the resulting spectra were treated in the same way to enable comparisons of assigned stoichiometric formulae between acquisitions.

RESULTS:

Converting the number of scans into micro-scans enhances signal quality by lowering noise and reducing artifacts. This modification also increases the number of attributed stoichiometric formulae for an equivalent acquisition time, giving access to a larger molecular diversity for the analyzed complex sample.

CONCLUSIONS:

For complex samples, the use of long acquisition times leads to optimal data quality, and the use of micro-scans instead of scans-only maximizes the number of attributed stoichiometric formulae.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Rapid Commun Mass Spectrom Año: 2020 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Rapid Commun Mass Spectrom Año: 2020 Tipo del documento: Article País de afiliación: Francia