Projects per year
Abstract
Infections caused by the Gram-negative pathogen Pseudomonas aeruginosa are emerging worldwide as a major threat to human health. Conventional antibiotic monotherapy suffers from rapid resistance development, underlining urgent need for novel treatment concepts. Here, we report on a nontraditional approach to combat P. aeruginosa-derived infections by targeting its main virulence factor, the elastase LasB. We discovered a new chemical class of phosphonates with an outstanding in vitro ADMET and PK profile, auspicious activity both in vitro and in vivo. We established the mode of action through a cocrystal structure of our lead compound with LasB and in several in vitro and ex vivo models. The proof of concept of a combination of our pathoblocker with levofloxacin in a murine neutropenic lung infection model and the reduction of LasB protein levels in blood as a proof of target engagement demonstrate the great potential for use as an adjunctive treatment of lung infections in humans.
Original language | English |
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Pages (from-to) | 2205-2215 |
Number of pages | 11 |
Journal | ACS Central Science |
Volume | 9 |
Issue number | 12 |
DOIs | |
Publication status | Published - 27 Dec 2023 |
Bibliographical note
Publisher Copyright:© 2023 The Authors. Published by American Chemical Society.
© 2023 The Authors. Published by American Chemical Society.
Keywords
- inhibitors
- LasB
Fields of Science and Technology Classification 2012
- 104 Chemistry
- 106 Biology
Projects
- 1 Finished
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Mechanism of bacterial collagenolysis
Schönauer, E. (Principal Investigator)
1/04/19 → 31/03/23
Project: Research