NACDDB - The Web Server for DNA,RNA,and Hybrids Circular Dichroism Structure

Collection and characterisation of bacterial membrane proteins

Overview of Saidijam M et al.

AuthorsSaidijam M  Psakis G  Clough JL  Meuller J  Suzuki S  Hoyle CJ  Palmer SL  Morrison SM  Pos MK  Essenberg RC  Maiden MC  Abu-bakr A  Baumberg SG  Neyfakh AA  Griffith JK  Stark MJ  Ward A  O'Reilly J  Rutherford NG  Phillips-Jones MK  Henderson PJ  
AffiliationAstbury Centre for Structural Molecular Biology   University of Leeds   Leeds LS2 9JT   UK.  
JournalFEBS Lett
Year 2003

Abstract


A general strategy for the amplified expression in Escherichia coli of membrane transport and receptor proteins from other bacteria is described. As an illustration we report the cloning of the putative alpha-ketoglutarate membrane transport gene from the genome of Helicobacter pylori, overexpression of the protein tagged with RGS(His)6 at the C-terminus, and its purification in mg quantities. The retention of structural and functional integrity was verified by circular dichroism spectroscopy and reconstitution of transport activity. This strategy for overexpression and purification is extended to additional membrane proteins from H. pylori and from other bacteria.