1. Academic Validation
  2. Dysregulation of bacterial proteolytic machinery by a new class of antibiotics

Dysregulation of bacterial proteolytic machinery by a new class of antibiotics

  • Nat Med. 2005 Oct;11(10):1082-7. doi: 10.1038/nm1306.
Heike Brötz-Oesterhelt 1 Dieter Beyer Hein-Peter Kroll Rainer Endermann Christoph Ladel Werner Schroeder Berthold Hinzen Siegfried Raddatz Holger Paulsen Kerstin Henninger Julia E Bandow Hans-Georg Sahl Harald Labischinski
Affiliations

Affiliation

  • 1 Department of Anti-infectives, Bayer HealthCare AG, Pharma Research, Aprather Weg 18a, D-42096 Wuppertal, Germany. heike.broetz-oesterhelt@bayerhealthcare.com
Abstract

Here we show that a new class of antibiotics-acyldepsipeptides-has Antibacterial activity against Gram-positive bacteria in vitro and in several rodent models of Bacterial infection. The acyldepsipeptides are active against isolates that are resistant to Antibiotics in clinical application, implying a new target, which we identify as ClpP, the core unit of a major Bacterial protease complex. ClpP is usually tightly regulated and strictly requires a member of the family of Clp-ATPases and often further accessory proteins for proteolytic activation. Binding of acyldepsipeptides to ClpP eliminates these safeguards. The acyldepsipeptide-activated ClpP core is capable of proteolytic degradation in the absence of the regulatory Clp-ATPases. Such uncontrolled proteolysis leads to inhibition of Bacterial cell division and eventually cell death.

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