Gradient reconstitution of membrane proteins for solid-state NMR studies |
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Authors: | Denis Lacabanne Alons Lends Clément Danis Britta Kunert Marie-Laure Fogeron Vlastimil Jirasko Claire Chuilon Lauriane Lecoq Cédric Orelle Vincent Chaptal Pierre Falson Jean-Michel Jault Beat H. Meier Anja Böckmann |
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Affiliation: | 1.Molecular Microbiology and Structural Biochemistry, Labex Ecofect,UMR 5086 CNRS-Université de Lyon, IBCP,Lyon,France;2.Physical Chemistry,ETH Zurich,Zurich,Switzerland |
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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. |
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