Binding of SecA ATPase monomers and dimers to lipid vesicles.

ABSTRACT: The Escherichia coli SecA ATPase motor protein is essential for secretion of proteins through the SecYEG translocon into the periplasmic space. Its function relies upon interactions with the surrounding lipid bilayer as well as SecYEG translocon. That negatively charged lipids are required for bilayer binding has been known for >25 years, but little systematic quantitative data is available. We have carried out an extensive investigation of SecA partitioning into large unilamellar vesicles (LUV) using a wide range of lipid and electrolyte compositions, including the principal cytoplasmic salt of E. coli, potassium glutamate, which we have shown stabilizes SecA. The water-to-bilayer transfer free energy is about -7.5 kcal mol^-1 for typical E. coli lipid compositions. Although it

SUBMITTER: Roussel G 

PROVIDER: S-EPMC6943190 | biostudies-literature | 2020 Feb

REPOSITORIES: biostudies-literature