Location, Location, Location: Establishing Design Principles for New Antibacterials from Ferric Siderophore Transport Systems

被引:1
|
作者
Luo, Vivien Canran [1 ]
Peczuh, Mark W. [1 ]
机构
[1] Univ Connecticut, Dept Chem, 55 N Eagleville Rd, U3060, Storrs, CT 06269 USA
来源
MOLECULES | 2024年 / 29卷 / 16期
关键词
iron transport; siderophore; Trojan Horse; antibiotics; cefiderocol; BETA-LACTAM ANTIBIOTICS; RESISTANT ACINETOBACTER-BAUMANNII; MEDIATED IRON TRANSPORT; PSEUDOMONAS-AERUGINOSA PAO1; ESCHERICHIA-COLI; OUTER-MEMBRANE; CRYSTAL-STRUCTURE; MOLECULAR-BASIS; IN-VITRO; FERRIPYOVERDINE RECEPTOR;
D O I
10.3390/molecules29163889
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This review strives to assemble a set of molecular design principles that enables the delivery of antibiotic warheads to Gram-negative bacterial targets (ESKAPE pathogens) using iron-chelating siderophores, known as the Trojan Horse strategy for antibiotic development. Principles are derived along two main lines. First, archetypical siderophores and their conjugates are used as case studies for native iron transport. They enable the consideration of the correspondence of iron transport and antibacterial target location. The second line of study charts the rationale behind the clinical antibiotic cefiderocol. It illustrates the potential versatility for the design of new Trojan Horse-based antibiotics. Themes such as matching the warhead to a location where the siderophore delivers its cargo (i.e., periplasm vs. cytoplasm), whether or not a cleavable linker is required, and the relevance of cheaters to the effectiveness and selectivity of new conjugates will be explored. The effort to articulate rules has identified gaps in the current understanding of iron transport pathways and suggests directions for new investigations.
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页数:40
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