Dynamic force spectroscopy of the Helicobacter pylori BabA-Lewis b binding

Biophys Chem. 2009 Jul;143(1-2):102-5. doi: 10.1016/j.bpc.2009.03.007. Epub 2009 Mar 19.

Abstract

The binding strength of the Helicobacter pylori adhesin-receptor complex BabA-ABO/Lewis b has been analyzed by means of dynamic force spectroscopy. High-resolution measurements of rupture forces were performed in situ on single bacterial cells, expressing the high-affinity binding BabA adhesin, by the use of force measuring optical tweezers. The resulting force spectra revealed the mechanical properties of a single BabA-Leb bond. It was found that the bond is dominated by one single energy barrier and that it is a slip-bond. The bond length and thermal off-rate were assessed to be 0.86+/-0.07 nm and 0.015+/-0.006 s(-1), respectively.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ABO Blood-Group System / metabolism
  • Adhesins, Bacterial / metabolism*
  • Glycoconjugates / chemistry
  • Glycoconjugates / metabolism
  • Helicobacter pylori / metabolism*
  • Humans
  • Kinetics
  • Lewis Blood Group Antigens / metabolism*
  • Models, Biological
  • Optical Tweezers
  • Protein Binding
  • Spectrum Analysis

Substances

  • ABO Blood-Group System
  • Adhesins, Bacterial
  • BabA protein, Helicobacter pylori
  • Glycoconjugates
  • Lewis Blood Group Antigens