DI-UMONS : Dépôt institutionnel de l’université de Mons

Recherche transversale
(titres de publication, de périodique et noms de colloque inclus)
2015-09-10 - Article/Dans un journal avec peer-review - Anglais - 12 page(s)

Demeyer Marie, Wisztorski Maxence, Decroo Corentin , De Winter Julien , Caulier Guillaume , Hennebert Elise , Eeckhaut Igor , Fournier Isabelle, Flammang Patrick , Gerbaux Pascal , "Inter- and intra-organ spatial distributions of sea star saponins by MALDI imaging" in Analytical and Bioanalytical Chemistry, 407, 8813-8824

  • Edition : Springer Science & Business Media B.V., Berlin (Germany)
  • Codes CREF : Chimie organique (DI1313), Biologie (DI3100)
  • Unités de recherche UMONS : Synthèse et spectrométrie de masse organiques (S836), Biologie des Organismes Marins et Biomimétisme (S864)
  • Instituts UMONS : Institut des Biosciences (Biosciences)
Texte intégral :

Abstract(s) :

(Anglais) Saponins are secondary metabolites that are abundant and diversified in echinoderms. Mass spectrometry is increasingly used not only to identify saponin congeners within animal extracts but also to decipher the structure/biological activity relationships of these molecules by determining their inter-organ and inter-individual variability. The usual method requires extensive purification procedures to prepare saponin extracts compatible with mass spectrometry analysis. Here, we selected the sea star Asterias rubens as a model animal to prove that direct analysis of saponins can be performed on tissue sections. We also demonstrated that carboxymethyl cellulose can be used as an embedding medium to facilitate the cryosectioning procedure. Matrix-assisted laser desorption/ionization (MALDI) imaging was also revealed to afford interesting data on the distribution of saponin molecules within the tissues. We indeed highlight that saponins are located not only inside the body wall of the animals but also within the mucus layer that probably protects the animal against external aggressions. Graphical Abstract Saponins are the most abundant secondary metabolites in sea stars. They should therefore participate in important biological activities. Here, MALDI imaging is presented as a powerful method to determine the spatial distribution of saponins within the animal tissues. The inhomogeneity of the intra-organ saponin distribution is highlighted, paving the way for future elegant structure/activity relationship investigations.