4.3 Article

Micro-coil NMR to monitor optimization of the reconstitution conditions for the integral membrane protein OmpW in detergent micelles

Journal

JOURNAL OF BIOMOLECULAR NMR
Volume 54, Issue 2, Pages 129-133

Publisher

SPRINGER
DOI: 10.1007/s10858-012-9658-x

Keywords

Structural biology; Integral membrane proteins; Solubilization in detergent micelles; E. coli outer membrane protein W

Funding

  1. Joint Center for Innovative Membrane Protein Technologies (JCIMPT-complexes, NIH Roadmap) [P50 GM073197]

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Optimization of aqueous solutions of the integral membrane protein (IMP) OmpW for NMR structure determination has been monitored with micro-coil NMR, which enables the acquisition of NMR spectra using only micrograms of protein and detergent. The detergent 30-Fos (2-undecylphosphocholine) was found to yield the best 2D [N-15, H-1]-TROSY correlation NMR spectra of [H-2, N-15]-labeled OmpW. For the OmpW structure determination we then optimized the 30-Fos concentration, the sample temperature and long-time stability, and the deuteration level of the protein. Some emerging guidelines for reconstitution of beta-barrel integral membrane proteins in structural biology are discussed.

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