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The structure of the bacterial iron–catecholate transporter Fiu suggests that it imports substrates via a two-step mechanism
The ferric iron uptake (Fiu) transporter from Escherichia coli functions in the transport of iron–catecholate complexes across the bacterial outer membrane, providing the bacterium with iron, which is essential for growth. Recently it has become clear that Fiu also represents a liability for E. coli...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6926462/ https://www.ncbi.nlm.nih.gov/pubmed/31712312 http://dx.doi.org/10.1074/jbc.RA119.011018 |
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author | Grinter, Rhys Lithgow, Trevor |
author_facet | Grinter, Rhys Lithgow, Trevor |
author_sort | Grinter, Rhys |
collection | PubMed |
description | The ferric iron uptake (Fiu) transporter from Escherichia coli functions in the transport of iron–catecholate complexes across the bacterial outer membrane, providing the bacterium with iron, which is essential for growth. Recently it has become clear that Fiu also represents a liability for E. coli because its activity allows import of antimicrobial compounds that mimic catecholate. This inadvertent import suggests the potential utility of antimicrobial catechol siderophore mimetics in managing bacterial infections. However, to fully exploit these compounds, a detailed understanding of the mechanism of transport through Fiu and related transporters is required. To address this question, we determined the crystal structure of Fiu at 2.1–2.9 Å and analyzed its function in E. coli. Through analysis of the Fiuo crystal structure, in combination with in silico docking and mutagenesis, we provide insight into how Fiu and related transporters bind catecholate in a surface-exposed cavity. Moreover, through determination of the structure of Fiu in multiple crystal states, we revealed the presence of a large, selectively gated cavity in the interior of this transporter. This chamber is large enough to accommodate the Fiu substrate and may allow import of substrates via a two-step mechanism. This would avoid channel formation through the transporter and inadvertent import of toxic molecules. As Fiu and its homologs are the targets of substrate-mimicking antibiotics, these results may assist in the development of these compounds. |
format | Online Article Text |
id | pubmed-6926462 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-69264622019-12-24 The structure of the bacterial iron–catecholate transporter Fiu suggests that it imports substrates via a two-step mechanism Grinter, Rhys Lithgow, Trevor J Biol Chem Protein Structure and Folding The ferric iron uptake (Fiu) transporter from Escherichia coli functions in the transport of iron–catecholate complexes across the bacterial outer membrane, providing the bacterium with iron, which is essential for growth. Recently it has become clear that Fiu also represents a liability for E. coli because its activity allows import of antimicrobial compounds that mimic catecholate. This inadvertent import suggests the potential utility of antimicrobial catechol siderophore mimetics in managing bacterial infections. However, to fully exploit these compounds, a detailed understanding of the mechanism of transport through Fiu and related transporters is required. To address this question, we determined the crystal structure of Fiu at 2.1–2.9 Å and analyzed its function in E. coli. Through analysis of the Fiuo crystal structure, in combination with in silico docking and mutagenesis, we provide insight into how Fiu and related transporters bind catecholate in a surface-exposed cavity. Moreover, through determination of the structure of Fiu in multiple crystal states, we revealed the presence of a large, selectively gated cavity in the interior of this transporter. This chamber is large enough to accommodate the Fiu substrate and may allow import of substrates via a two-step mechanism. This would avoid channel formation through the transporter and inadvertent import of toxic molecules. As Fiu and its homologs are the targets of substrate-mimicking antibiotics, these results may assist in the development of these compounds. American Society for Biochemistry and Molecular Biology 2019-12-20 2019-11-11 /pmc/articles/PMC6926462/ /pubmed/31712312 http://dx.doi.org/10.1074/jbc.RA119.011018 Text en © 2019 Grinter and Lithgow. Author's Choice—Final version open access under the terms of the Creative Commons CC-BY license (http://creativecommons.org/licenses/by/4.0) . |
spellingShingle | Protein Structure and Folding Grinter, Rhys Lithgow, Trevor The structure of the bacterial iron–catecholate transporter Fiu suggests that it imports substrates via a two-step mechanism |
title | The structure of the bacterial iron–catecholate transporter Fiu suggests that it imports substrates via a two-step mechanism |
title_full | The structure of the bacterial iron–catecholate transporter Fiu suggests that it imports substrates via a two-step mechanism |
title_fullStr | The structure of the bacterial iron–catecholate transporter Fiu suggests that it imports substrates via a two-step mechanism |
title_full_unstemmed | The structure of the bacterial iron–catecholate transporter Fiu suggests that it imports substrates via a two-step mechanism |
title_short | The structure of the bacterial iron–catecholate transporter Fiu suggests that it imports substrates via a two-step mechanism |
title_sort | structure of the bacterial iron–catecholate transporter fiu suggests that it imports substrates via a two-step mechanism |
topic | Protein Structure and Folding |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6926462/ https://www.ncbi.nlm.nih.gov/pubmed/31712312 http://dx.doi.org/10.1074/jbc.RA119.011018 |
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