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dc.rights.licenseopenen_US
dc.contributor.authorAL HAMOUI DIT BANNI, G.
dc.contributor.authorNASREDDINE, R.
hal.structure.identifierUnité de Recherche Oenologie [Villenave d'Ornon] [OENO]
dc.contributor.authorFAYAD, Syntia
dc.contributor.authorCOLAS, C.
hal.structure.identifierUnité de Recherche Oenologie [Villenave d'Ornon] [OENO]
dc.contributor.authorMARCHAL, Axel
dc.contributor.authorNEHME, R.
dc.date.accessioned2021-12-16T10:24:53Z
dc.date.available2021-12-16T10:24:53Z
dc.date.issued2021
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/124183
dc.description.abstractEnThe evaluation of binding affinities between large biomolecules and small ligands is challenging and requires highly sensitive techniques. Microscale thermophoresis (MST) is an emerging biophysical technique used to overcome this limitation. This work describes the first MST binding method to evaluate binding affinities of small ligands to lipases from crude porcine pancreatic extracts. The conditions of the MST assay were thoroughly optimized to successfully evaluate the dissociation constant (Kd) between pancreatic lipases (PL) and triterpenoid compounds purified from oakwood. More precisely, the fluorescent labeling of PL (PL*) using RED-NHS dye was achieved via a buffer exchange procedure. The MST buffer was composed of 20 mM NaH2PO4 + 77 mM NaCl (pH 6.6) with 0.05% Triton-X added to efficiently prevent protein aggregation and adsorption, even when using only standard, uncoated MST capillaries. Storage at -20°C ensured stability of PL* and its fluorescent signal. MST results showed that crude pancreatic extracts were suitable as a source of PL for the evaluation of binding affinities of small ligands. Quercotriterpenoside-I (QTT-I) demonstrated high PL* binding affinity (31 nM) followed by 3-O-galloylbarrinic acid (3-GBA) (500 nM) and bartogenic acid (BA) (1327 nM). To enrich the 50 kDa lipase responsible for the majority of hydrolysis activity in the crude pancreatic extracts, ammonium sulfate precipitation was attempted and its efficiency confirmed using capillary electrophoresis (CE)-based activity assays and HRMS. Moreover, to accurately explain enzyme modulation mechanism, it is imperative to complement binding assays with catalytic activity ones.
dc.description.sponsorshipSynthèse Organique : des molécules au vivant - ANR-11-LABX-0029en_US
dc.language.isoENen_US
dc.subject.enBinding affinity
dc.subject.enCapillary electrophoresis
dc.subject.enEnzymatic assays
dc.subject.enHigh-resolution mass spectrometry
dc.subject.enLipase
dc.subject.enMicroscale thermophoresis
dc.title.enInvestigation of lipase-ligand interactions in porcine pancreatic extracts by microscale thermophoresis
dc.typeArticle de revueen_US
dc.identifier.doi10.1007/s00216-021-03314-7en_US
dc.subject.halSciences du Vivant [q-bio]/Biologie végétaleen_US
bordeaux.journalAnalytical and Bioanalytical Chemistryen_US
bordeaux.page3667-3681en_US
bordeaux.volume413en_US
bordeaux.hal.laboratoriesUnité de Recherche Oenologie - EA 4577en_US
bordeaux.issue14en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionINRAEen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.identifier.funderIDConseil Régional du Centre-Val de Loireen_US
hal.exportfalse
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Analytical%20and%20Bioanalytical%20Chemistry&rft.date=2021&rft.volume=413&rft.issue=14&rft.spage=3667-3681&rft.epage=3667-3681&rft.au=AL%20HAMOUI%20DIT%20BANNI,%20G.&NASREDDINE,%20R.&FAYAD,%20Syntia&COLAS,%20C.&MARCHAL,%20Axel&rft.genre=article


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