Structural basis for antibacterial peptide self-immunity by the bacterial ABC transporter McjD.
Structural basis for antibacterial peptide self-immunity by the bacterial ABC transporter McjD.
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DOI:
10.15252/embj.201797278
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发表时间:
2017-10-16
期刊:
影响因子:
--
通讯作者:
Beis K
中科院分区:
文献类型:
--
作者:
Bountra K;Hagelueken G;Choudhury HG;Corradi V;El Omari K;Wagner A;Mathavan I;Zirah S;Yuan Wahlgren W;Tieleman DP;Schiemann O;Rebuffat S;Beis K
Certain pathogenic bacteria produce and release toxic peptides to ensure either nutrient availability or evasion from the immune system. These peptides are also toxic to the producing bacteria that utilize dedicated ABC transporters to provide self‐immunity. The ABC transporter McjD exports the antibacterial peptide MccJ25 in Escherichia coli. Our previously determined McjD structure provided some mechanistic insights into antibacterial peptide efflux. In this study, we have determined its structure in a novel conformation, apo inward‐occluded and a new nucleotide‐bound state, high‐energy outward‐occluded intermediate state, with a defined ligand binding cavity. Predictive cysteine cross‐linking in E. coli membranes and PELDOR measurements along the transport cycle indicate that McjD does not undergo major conformational changes as previously proposed for multi‐drug ABC exporters. Combined with transport assays and molecular dynamics simulations, we propose a novel mechanism for toxic peptide ABC exporters that only requires the transient opening of the cavity for release of the peptide. We propose that shielding of the cavity ensures that the transporter is available to export the newly synthesized peptides, preventing toxic‐level build‐up.
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影响因子:
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作者:
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通讯作者:
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DOI:
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发表时间:
2006-01-01
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发表时间:
2004-12-01
影响因子:
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DOI:
10.1107/s0907444904016427
发表时间:
2004-12-01
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