Gradient reconstitution of membrane proteins for solid-state NMR studies
Creators
- 1. UMR 5086 CNRS-Université de Lyon, IBCP, Molecular Microbiology and Structural Biochemistry, Labex Ecofect (France)
- 2. ETH Zurich, Physical Chemistry (Switzerland)
Description
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.
Additional details
Identifiers
Publishing Information
- Journal Title
- Journal of Biomolecular NMR
- Journal Volume
- 69
- Journal Issue
- 2
- Journal Page Range
- p. 81-91
- ISSN
- 0925-2738
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 49106712
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- ELECTRON MICROSCOPY; MEMBRANE PROTEINS; NUCLEAR MAGNETIC RESONANCE; SAMPLE PREPARATION
- Descriptors DEC
- MAGNETIC RESONANCE; MICROSCOPY; ORGANIC COMPOUNDS; PROTEINS; RESONANCE
Optional Information
- Copyright
- Copyright (c) 2017 Springer Science+Business Media B.V.