CRC 1009 B03 - Autopenetration of bacterial effector proteins and modulation of signalling responses in cellular barriers

Basic data for this project

Type of projectSubproject in DFG-joint project hosted at University of Münster
Duration at the University of Münster01/07/2020 - 30/06/2024 | 3rd Funding period

Description

Effector proteins can also enter host cells in a type III secretion system (T3SS)-independent manner thereby widening their potential functional range to modulate cellular barriers. In this regard, we identified the entire group of bacterial leucine-rich repeat (LPX) effector proteins as so far unknown cell-penetrating effector proteins (CPE), which provided further evidence for a general concept of T3SS-independent translocation. Now we will elucidate the effects of this novel class of CPE in modulating immune responses in cell-culture and animal models and explore potential therapeutic applications of these CPE.

KeywordsMedical Microbiology; Mycology; Hygiene; Molecular Infection Biology
Website of the projecthttps://www.medizin.uni-muenster.de/en/sfb-1009/projects/project-area-b/b-03.html
Funding identifierSFB 1009/3, B03
Funder / funding scheme
  • DFG - Collaborative Research Centre (SFB)

Project management at the University of Münster

Rüter, Christian
Institute of Infectiology

Applicants from the University of Münster

Rüter, Christian
Institute of Infectiology