Structural basis for binding and transfer of heme in bacterial heme-acquisition systems.
Proteins
; 85(12): 2217-2230, 2017 Dec.
Article
em En
| MEDLINE
| ID: mdl-28913898
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.
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Base de dados:
MEDLINE
Assunto principal:
Proteínas Periplásmicas de Ligação
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Chloroflexi
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Burkholderia cenocepacia
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Heme
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Ferro
Idioma:
En
Ano de publicação:
2017
Tipo de documento:
Article