| Literature DB >> 28900789 |
Denis Lacabanne1, Alons Lends2, Clément Danis1, Britta Kunert1, Marie-Laure Fogeron1, Vlastimil Jirasko2, Claire Chuilon1, Lauriane Lecoq1, Cédric Orelle1, Vincent Chaptal1, Pierre Falson1, Jean-Michel Jault1, Beat H Meier3, Anja Böckmann4.
Abstract
We here adapted the GRecon method used in electron microscopy studies for membrane protein reconstitution to the needs of solid-state NMR sample preparation. We followed in detail the reconstitution of the ABC transporter BmrA by dialysis as a reference, and established optimal reconstitution conditions using the combined sucrose/cyclodextrin/lipid gradient characterizing GRecon. We established conditions under which quantitative reconstitution of active protein at low lipid-to-protein ratios can be obtained, and also how to upscale these conditions in order to produce adequate amounts for NMR. NMR spectra recorded on a sample produced by GRecon showed a highly similar fingerprint as those recorded previously on samples reconstituted by dialysis. GRecon sample preparation presents a gain in time of nearly an order of magnitude for reconstitution, and shall represent a valuable alternative in solid-state NMR membrane protein sample preparation.Entities:
Keywords: ABC-transporter; BmrA; Membrane proteins reconstitution; Solid-state NMR
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Year: 2017 PMID: 28900789 DOI: 10.1007/s10858-017-0135-4
Source DB: PubMed Journal: J Biomol NMR ISSN: 0925-2738 Impact factor: 2.835