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Active NON-SBIR/STTR RPGS NIH (US)

Molecular Mechanism of an Exporter-like ABC Importer YbtPQ

$4.99M USD

Funder NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
Recipient Organization University of Colorado Denver
Country United States
Start Date Jul 17, 2024
End Date May 31, 2029
Duration 1,779 days
Number of Grantees 1
Roles Principal Investigator
Data Source NIH (US)
Grant ID 10877484
Grant Description

Bacterial infections pose one of the most significant global public health challenges, exacerbated by the emergence of antibiotic-resistant strains. As a result, treating these infections has become increasingly difficult. Recently, the FDA approved cefiderocol, a siderophore-antibiotic conjugate, as a new treatment for urinary tract

infections (UTIs) caused by antibiotic-resistant Gram-negative bacteria. This approval highlights the potential of targeting the bacterial siderophore-mediated metal uptake process for pharmaceutical interventions. A crucial step in this process involves the uptake of metal-chelated siderophores across the bacterial inner membrane,

facilitated by ATP-binding cassette (ABC) importers. Unfortunately, the detailed molecular mechanisms underlying these importers remains poorly understood, impeding the development of targeted drugs. This proposal focuses on a unique example of these critical importers: the yersiniabactin importer YbtPQ from

uropathogenic E. coli, the leading cause of UTIs. Our preliminary studies have revealed that YbtPQ exhibits folding characteristics similar to an ABC exporter, representing a novel type of ABC transporter. Building upon this discovery, we expect to study the fundamental structure-function relationship of YbtPQ by pursuing two

specific aims: 1) Define the substrate selectivity and inhibitory mechanism of YbtPQ; 2) Understand the unique structural motifs within YbtPQ. To accomplish these goals, we will employ a multidisciplinary approach, combining mutagenesis, specifically-designed transport assays, microscale thermophoresis, circular dichroism,

native mass spectrometry, molecular dynamic simulations, and cryo-electron microscopy. Successful completion of this proposal will yield valuable insights into the substrate/inhibitor selectivity and transport dynamics of YbtPQ. This knowledge will serve as a solid foundation for future drug development targeting this importer, offering new

possibilities for effectively treating bacterial infections and addressing the challenges of antibiotic resistance.

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University of Colorado Denver

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