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Gradient reconstitution of membrane proteins for solid-state NMR studies.

Authors :
Lacabanne D
Lends A
Danis C
Kunert B
Fogeron ML
Jirasko V
Chuilon C
Lecoq L
Orelle C
Chaptal V
Falson P
Jault JM
Meier BH
Böckmann A
Source :
Journal of biomolecular NMR [J Biomol NMR] 2017 Oct; Vol. 69 (2), pp. 81-91. Date of Electronic Publication: 2017 Sep 12.
Publication Year :
2017

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.

Details

Language :
English
ISSN :
1573-5001
Volume :
69
Issue :
2
Database :
MEDLINE
Journal :
Journal of biomolecular NMR
Publication Type :
Academic Journal
Accession number :
28900789
Full Text :
https://doi.org/10.1007/s10858-017-0135-4