Expression and purification of FtsW and RodA from Streptococcus pneumoniae, two membrane proteins involved in cell division and cell growth, respectively

Marjolaine Noirclerc-Savoye (1, 2, 3) , Cécile Morlot (1, 2, 3) , Philippe Gerard (4, 1, 2, 3) , Thierry Vernet (1, 2, 3) , André Zapun (1, 2, 3)

1 LIM - Laboratoire d'Ingénierie des Macromolécules
2 CNRS - Centre National de la Recherche Scientifique
3 UJF - Université Joseph Fourier - Grenoble 1
4 UEPSD - Unité de recherche d'Écologie et Physiologie du Système Digestif

FtsW and RodA are homologous integral membrane proteins involved in bacterial cell division and cell growth, respectively. Both proteins from Streptococcus pneumoniae were overexpressed in Escherichia coli as N-terminal His-tagged fusions. Their membrane addressing in E. coli was demonstrated by cell fractionation and was confirmed for FtsW by immunolocalization. Recombinant FtsW and RodA were solubilized from membranes using 3-(laurylamido)-N,N'-dimethylaminopropylamine oxide (LAPAO). The detergent was exchanged to polyoxyethylene 8 lauryl ether (C12E8) during one-step purification procedure by Co(2+)-affinity chromatography. This procedure yielded 50-150 microg protein per litre of culture. Both proteins are likely to be folded as they are resistant to trypsin digestion and could be incorporated into reconstituted lipid vesicles.

Domaines: Sciences du Vivant [q-bio]

Marjolaine Noirclerc-Savoye, Cécile Morlot, Philippe Gerard, Thierry Vernet, André Zapun. Expression and purification of FtsW and RodA from Streptococcus pneumoniae, two membrane proteins involved in cell division and cell growth, respectively. Protein Expression and Purification, 2003, 30 (1), pp.18-25. ⟨10.1016/S1046-5928(03)000⟩. ⟨hal-01601007⟩