| Literature DB >> 22890565 |
Pawel Stanczak1, Qinghai Zhang, Reto Horst, Pedro Serrano, Kurt Wüthrich.
Abstract
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 [(15)N, (1)H]-TROSY correlation NMR spectra of [(2)H, (15)N]-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 β-barrel integral membrane proteins in structural biology are discussed.Entities:
Mesh:
Substances:
Year: 2012 PMID: 22890565 PMCID: PMC3715323 DOI: 10.1007/s10858-012-9658-x
Source DB: PubMed Journal: J Biomol NMR ISSN: 0925-2738 Impact factor: 2.835