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8ADI

Cryo-EM structure of Darobactin 9 bound BAM complex

Summary for 8ADI
Entry DOI10.2210/pdb8adi/pdb
EMDB information15363
Related PRD IDPRD_002430
DescriptorOuter membrane protein assembly factor BamA, Outer membrane protein assembly factor BamB, Outer membrane protein assembly factor BamC, ... (6 entities in total)
Functional Keywordsbam complex; darobactin 9, structural protein
Biological sourceEscherichia coli
More
Total number of polymer chains6
Total formula weight214349.35
Authors
Yuan, B.,Marlovits, T.C. (deposition date: 2022-07-08, release date: 2023-01-11, Last modification date: 2024-11-20)
Primary citationSeyfert, C.E.,Porten, C.,Yuan, B.,Deckarm, S.,Panter, F.,Bader, C.D.,Coetzee, J.,Deschner, F.,Tehrani, K.H.M.E.,Higgins, P.G.,Seifert, H.,Marlovits, T.C.,Herrmann, J.,Muller, R.
Darobactins Exhibiting Superior Antibiotic Activity by Cryo-EM Structure Guided Biosynthetic Engineering.
Angew.Chem.Int.Ed.Engl., 62:e202214094-e202214094, 2023
Cited by
PubMed Abstract: Over recent decades, the pipeline of antibiotics acting against Gram-negative bacteria is running dry, as most discovered candidate antibiotics suffer from insufficient potency, pharmacokinetic properties, or toxicity. The darobactins, a promising new small peptide class of drug candidates, bind to novel antibiotic target BamA, an outer membrane protein. Previously, we reported that biosynthetic engineering in a heterologous host generated novel darobactins with enhanced antibacterial activity. Here we utilize an optimized purification method and present cryo-EM structures of the Bam complex with darobactin 9 (D9), which served as a blueprint for the biotechnological generation of twenty new darobactins including halogenated analogs. The newly engineered darobactin 22 binds more tightly to BamA and outperforms the favorable activity profile of D9 against clinically relevant pathogens such as carbapenem-resistant Acinetobacter baumannii up to 32-fold, without observing toxic effects.
PubMed: 36308277
DOI: 10.1002/anie.202214094
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.4 Å)
Structure validation

236620

數據於2025-05-28公開中

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