Published October 2017 | Version v1
Journal article

Gradient reconstitution of membrane proteins for solid-state NMR studies

  • 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.