Hydrogenated Diglucose Detergents for Membrane-Protein Extraction and Stabilization
journal contributionposted on 15.02.2019, 00:00 by Pierre Guillet, Florian Mahler, Kelly Garnier, Gildas Nyame Mendendy Boussambe, Sébastien Igonet, Carolyn Vargas, Christine Ebel, Marine Soulié, Sandro Keller, Anass Jawhari, Grégory Durand
We report herein the design and synthesis of a novel series of alkyl glycoside detergents consisting of a nonionic polar headgroup that comprises two glucose moieties in a branched arrangement (DG), onto which octane-, decane-, and dodecanethiols were grafted leading to ODG, DDG, and DDDG detergents, respectively. Micellization in aqueous solution was studied by isothermal titration calorimetry, 1H NMR spectroscopy, and surface tensiometry. Critical micellar concentration values were found to decrease by a factor of ∼10 for each pair of methylene groups added to the alkyl chain, ranging from ∼0.05 to 9 mM for DDDG and ODG, respectively. Dynamic light scattering and analytical ultracentrifugation sedimentation velocity experiments were used to investigate the size and composition of the micellar aggregates, showing that the aggregation number significantly increased from ∼40 for ODG to ∼80 for DDDG. All new compounds were able to solubilize membrane proteins (MPs) from bacterial membranes, insect cells, as well as the Madin–Darby canine kidney cells. In particular, native human adenosine receptor (A2AR) and bacterial transporter (BmrA) were solubilized efficiently. Striking thermostability improvements of +13 and +8 °C were observed when ODG and DDG were, respectively, applied to wild-type and full-length A2AR. Taken together, this novel detergent series shows promising detergent potency for solubilization and stabilization of membrane proteins (MPs) and thus makes a valuable addition to the chemical toolbox available for extracting and handling these important but challenging MP targets.
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Critical micellar concentration valueschemical toolboxalkyl chain1 H NMR spectroscopyadenosine receptoralkyl glycoside detergentsglucose moietiesmembrane proteinsaggregation numberHydrogenated Diglucose DetergentsDynamic lightmicellar aggregatestitration calorimetrymethylene groupsnovel seriessurface tensiometryMembrane-Protein Extractionthermostability improvements9 mMdetergent potencyMP targetsinsect cellskidney cellssolubilize membrane proteinsultracentrifugation sedimentation velocity experiments2ARODGnovel detergent seriesDDDG detergents