TY - JOUR A1 - Poyraz, Ö. A1 - Schmidt, H. A1 - Seidel, K. A1 - Delißen, Friedmar A1 - Ader, C. A1 - Tenenboim, H. A1 - Goosmann, C. A1 - Laube, B. A1 - Thünemann, Andreas A1 - Zychlinsky, A. A1 - Baldus, M. A1 - Lange, A. A1 - Griesinger, C. A1 - Kolbe, M. T1 - Protein refolding is required for assembly of the type three secretion needle N2 - Pathogenic Gram-negative bacteria use a type three secretion system (TTSS) to deliver virulence factors into host cells. Although the order in which proteins incorporate into the growing TTSS is well described, the underlying assembly mechanisms are still unclear. Here we show that the TTSS needle protomer refolds spontaneously to extend the needle from the distal end. We developed a functional mutant of the needle protomer from Shigella flexneri and Salmonella typhimurium to study its assembly in vitro. We show that the protomer partially refolds from α-helix into β-strand conformation to form the TTSS needle. Reconstitution experiments show that needle growth does not require ATP. Thus, like the structurally related flagellar systems, the needle elongates by subunit polymerization at the distal end but requires protomer refolding. Our studies provide a starting point to understand the molecular assembly mechanisms and the structure of the TTSS at atomic level. PY - 2010 U6 - https://doi.org/10.1038/nsmb.1822 SN - 1545-9993 SN - 1545-9985 VL - 17 SP - 788 EP - 792 PB - Nature Publ. Comp. CY - New York, NY, USA AN - OPUS4-21726 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -