June 13, 2010
Every day the human organism is confronted with a huge variety of pathogens (fig. 1). Most of them are fended off by our immune system. To execute a successful infection, bacteria must therefore manipulate the host to ensure their survival. They secrete virulence factors through a transport channel located in the bacterial membrane. Some bacteria, such as the causative agents of dysentery, food poisoning, typhoid fever, and pest, have developed a specialized transport mechanism called the Type three secretion system. Electron microscopy reveals that this structure is formed like a syringe: the base of the syringe is imbedded in the bacterial membrane, and the needle protrudes out of the bacteria (fig. 2). With this apparatus bacteria can inject virulence factors directly into the host cell.
So far, little has been known about how bacteria build this nano-syringe. Scientists from the Max Planck Institute for Infection Biology in Berlin, the Max Planck Institute for Biophysical Chemistry in Göttingen, and the Federal Institute for Materials Research and Testing have now succeeded in elucidating fundamental principles of the needle assembly. This was made possible by reconstitution experiments which allowed them to study the assembly of proteins into a needle in the test tube (fig. 3).
The close observation of these events revealed how the proteins are assembled into a syringe: the bacterium synthesizes the proteins in the cell interior, transports them through the syringe to the outside, and stacks them one after the other onto the tip of the growing needle. The scientists could also show that the proteins change their three-dimensional structure during the assembly process. They were able to pinpoint the exact structural changes down to the single amino acid level.
These results provide new perspectives in the development of medications that might interfere very early in the course of infection. These so-called anti-infectives could inhibit the assembly of the needle and the injection of virulence factors into the host cell. This would be a major advantage over antibiotics, which have to travel through the membrane into the bacteria to be able to kill it. Furthermore, antibiotics cannot distinguish between good and evil, i.e. disease-causing bacteria, often leading to unwanted side effects. Lastly, the use of anti-infectives would circumvent the problem of antibiotic resistance development.
The change of the three-dimensional structure of the proteins during the needle assembly was analyzed by X-ray structural experiments at BESSY in Berlin and ESRF in Grenoble and complementary NMR-spectroscopic experiments in liquid and solid phase at the Max Planck Institute for Biophysical Chemistry in Göttingen (Department Griesinger). The scientists compared the three-dimensional structure of the needle protein before and after the needle assembly.
BESSY (Berlin Electron Storage Ring Society for Synchrotron Radiation) and ESRF (European Synchrotron Radiation Facility, Grenoble): research facilities in which scientists from all over the world can use x-rays for structural analysis