Download MendeleyStructural basis for binding and transfer of heme in bacterial heme-acquisition systems.
Naoe, Y., Nakamura, N., Rahman, M.M., Tosha, T., Nagatoishi, S., Tsumoto, K., Shiro, Y., Sugimoto, H.(2017) Proteins 85: 2217-2230
- PubMed: 28913898
- DOI: https://doi.org/10.1002/prot.25386
- Primary Citation of Related Structures:
5GIZ, 5GJ3, 5Y89, 5Y8A, 5Y8B - PubMed Abstract:
Periplasmic heme-binding proteins (PBPs) in Gram-negative bacteria are components of the heme acquisition system. These proteins shuttle heme across the periplasmic space from outer membrane receptors to ATP-binding cassette (ABC) heme importers located in the inner-membrane. In the present study, we characterized the structures of PBPs found in the pathogen Burkholderia cenocepacia (BhuT) and in the thermophile Roseiflexus sp. RS-1 (RhuT) in the heme-free and heme-bound forms. The conserved motif, in which a well-conserved Tyr interacts with the nearby Arg coordinates on heme iron, was observed in both PBPs. The heme was recognized by its surroundings in a variety of manners including hydrophobic interactions and hydrogen bonds, which was confirmed by isothermal titration calorimetry. Furthermore, this study of 3 forms of BhuT allowed the first structural comparison and showed that the heme-binding cleft of BhuT adopts an "open" state in the heme-free and 2-heme-bound forms, and a "closed" state in the one-heme-bound form with unique conformational changes. Such a conformational change might adjust the interaction of the heme(s) with the residues in PBP and facilitate the transfer of the heme into the translocation channel of the importer.
Organizational Affiliation:
Biometal Science Laboratory, RIKEN SPring-8 Center, 1-1-1 Kouto, Sayo, Hyogo, 679-5148, Japan.
