Shigella flexneri Spa15 crystal structure verified in solution by double electron electron resonance

J Mol Biol. 2011 Jan 14;405(2):427-35. doi: 10.1016/j.jmb.2010.10.053. Epub 2010 Nov 12.

Abstract

Shigella flexneri Spa15 is a chaperone of the type 3 secretion system, which binds a number of effectors to ensure their stabilization prior to secretion. One of these effectors is IpgB1, a mimic of the human Ras-like Rho guanosine triphosphatase RhoG. In this study, Spa15 alone and in complex with IpgB1 has been studied by double electron electron resonance, an experiment that gives distance information showing the spacial separation of attached spin labels. This distance is explained by determining the crystal structure of the spin-labeled Spa15 where labels are seen to be buried in hydrophobic pockets. The double electron electron resonance experiment on the Spa15 complex with IpgB1 shows that IpgB1 does not bind Spa15 in the same way as is seen in the homologous Salmonella sp. chaperone:effector complex InvB:SipA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / chemistry*
  • Bacterial Proteins / metabolism
  • Crystallography, X-Ray
  • Electron Spin Resonance Spectroscopy*
  • Electrons*
  • Models, Molecular
  • Molecular Chaperones / chemistry*
  • Molecular Chaperones / metabolism
  • Protein Conformation
  • Shigella flexneri / growth & development
  • Shigella flexneri / metabolism*
  • Solutions
  • Spin Labels
  • rac1 GTP-Binding Protein / chemistry
  • rac1 GTP-Binding Protein / metabolism

Substances

  • Bacterial Proteins
  • Molecular Chaperones
  • Solutions
  • Spa15 protein, Shigella flexneri
  • Spin Labels
  • IpgB1 protein, Shigella flexneri
  • rac1 GTP-Binding Protein