β-Lactamase cleavable antimicrobial peptide–drug conjugates

Antimicrobial resistance attracts a considerable amount of attention as it threatens the efficiency of current antibacterial treatments. Besides a more considerate use of current antibiotics to slow down the spread of antimicrobial resistance, there is ample need for new therapeutic avenues to treat already resistant strains. Here, we describe the use of a cleavable peptide-drug conjugate to target bacteria with diverse resistance strategies. The conjugate consists of three main components: a β-lactamase cleavable linker, a positively charged stapled antimicrobial peptide, and an antibiotic. The linker ensures selective cleavage and provides the prospect of lowering systemic toxicity of the conjugate. The positively charged peptide targets the negatively charged bacterial membrane, and stapling pre-organises it in a helical structure. Finally, the drug provides another, distinct mode of action to the peptide, which should overall reduce the development of resistance. A series of peptides was prepared and the most promising one was then developed into a stapled conjugate. The factors affecting the activity of this conjugate were investigated, proving cleavage by β-lactamase and superior potency compared to the non-cleavable control, as shown by its minimal inhibitory concentrations.

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Publication Details

Journal
Chemical Science
Published
2025-01-01
DOI
https://doi.org/10.1039/d5sc06369h
Primary Topic
Antimicrobial Peptides and Activities
Type
article
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article

β-Lactamase cleavable antimicrobial peptide–drug conjugates

Thomas A. Hunt, Kristina A. Kostadinova, Josephine Gaynord, Tomáš Deingruber et al.
Chemical Science
Antimicrobial Peptides and Activities
article

β-Lactamase cleavable antimicrobial peptide–drug conjugates

Thomas A. Hunt, Kristina A. Kostadinova, Josephine Gaynord, Tomáš Deingruber, Jeremy S. Parker, Martin Welch, Yaw Sing Tan, David R. Spring, Thomas O’Brien, Jason S. Carroll, Bee‐Ha Gan
article en

Abstract

Antimicrobial resistance attracts a considerable amount of attention as it threatens the efficiency of current antibacterial treatments. Besides a more considerate use of current antibiotics to slow down the spread of antimicrobial resistance, there is ample need for new therapeutic avenues to treat already resistant strains. Here, we describe the use of a cleavable peptide-drug conjugate to target bacteria with diverse resistance strategies. The conjugate consists of three main components: a β-lactamase cleavable linker, a positively charged stapled antimicrobial peptide, and an antibiotic. The linker ensures selective cleavage and provides the prospect of lowering systemic toxicity of the conjugate. The positively charged peptide targets the negatively charged bacterial membrane, and stapling pre-organises it in a helical structure. Finally, the drug provides another, distinct mode of action to the peptide, which should overall reduce the development of resistance. A series of peptides was prepared and the most promising one was then developed into a stapled conjugate. The factors affecting the activity of this conjugate were investigated, proving cleavage by β-lactamase and superior potency compared to the non-cleavable control, as shown by its minimal inhibitory concentrations.

Chemical ScienceVol. 16(41)
AstraZeneca (United Kingdom) (GB), Agency for Science, Technology and Research (SG), University of Cambridge (GB), Cancer Research UK (GB), Bioinformatics Institute (SG)
Openalex Percentile: Top 77%
Antimicrobial Peptides and Activities
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