Lipid−Protein Nanodiscs as Reference Medium in Detergent Screening for High-Resolution NMR Studies of Integral Membrane Proteins

The choice of a suitable detergent-based membrane mimetic is of crucial importance for high-resolution NMR studies of membrane proteins. The present report describes a new approach of detergent screening. It is based on the comparison of 2D 1H,15N-correlation spectra of a protein in a membrane-bilay...

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Veröffentlicht in:Journal of the American Chemical Society 2010-04, Vol.132 (16), p.5628-5629
Hauptverfasser: Shenkarev, Zakhar O, Lyukmanova, Ekaterina N, Paramonov, Alexander S, Shingarova, Lyudmila N, Chupin, Vladimir V, Kirpichnikov, Mikhail P, Blommers, Marcel J. J, Arseniev, Alexander S
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Sprache:eng
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Zusammenfassung:The choice of a suitable detergent-based membrane mimetic is of crucial importance for high-resolution NMR studies of membrane proteins. The present report describes a new approach of detergent screening. It is based on the comparison of 2D 1H,15N-correlation spectra of a protein in a membrane-bilayer “reference” medium and in “trial” detergent-based environments. The proposed “reference” medium is the lipid−protein nanodisc (LPN) representing nanoscale phospholipid bilayers wrapped around by apolipoprotein A-1. The set of zwitterionic (DPC, DMPC/DHPC), anionic (SDS, LMPG, LPPG), and weakly cationic (LDAO) detergent-based media was screened for their ability to represent the native structure of the isolated voltage-sensing domain (VSD) of the archaeal potassium channel KvAP. The VSD/LPN complexes composed of saturated zwitterionic (DMPC), anionic (DMPG), or a mixture of unsaturated differently charged (POPC/DOPG, 3:1) lipids were used as reference. All assayed detergent media demonstrate similar CD spectra of the domain with a high level (∼60%) of overall helicity but different 2D NMR spectra. Using the reference spectrum of the VSD in LPN, we were able to choose the detergent composition in which the membrane-like structure of the VSD is preserved.
ISSN:0002-7863
1520-5126
DOI:10.1021/ja9097498