| Literature DB >> 24510648 |
S Saif Hasan1, Danas Baniulis1,2, Eiki Yamashita3, Mariya V Zhalnina1, Stanislav D Zakharov1,4, Jason T Stofleth1,5, William A Cramer1.
Abstract
Methods for studying interactions of protein with lipids and detergents are described for representatives of two major classes of membrane proteins: (1) the α-helical hetero-oligomeric integral cytochrome b6 f complex of oxygenic photosynthesis from cyanobacteria, and (2) the outer membrane β-barrel proteins BtuB and OmpF from Gram-negative Escherichia coli bacteria. Details are presented on the use of detergents for purification and crystallization of the b6 f complex as well as a method for lipid exchange. The positions of detergent and lipid molecules, which define eight potential lipid-binding sites in the b6 f complex, are described. Differences in detergent strategies for isolation and crystallization of β-barrel proteins relative to those for oligomeric helical membrane proteins are discussed, and purification and assessment of protein quality by circular dichroism (CD) is presented.Entities:
Keywords: BtuB; OmpF porin; cytochrome b6f complex; vitamin B12 receptor
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Year: 2013 PMID: 24510648 PMCID: PMC4062877 DOI: 10.1002/0471140864.ps2907s74
Source DB: PubMed Journal: Curr Protoc Protein Sci ISSN: 1934-3655