CLiB - a novel cardiolipin-binder isolated via data-driven and in vitro screening

Open Access
Authors
  • I. Kleinwächter
  • B. Mohr
  • A. Joppe
  • N. Hellmann
  • T. Bereau ORCID logo
  • H.D. Osiewacz
  • D. Schneider
Publication date 01-07-2022
Journal RSC Chemical Biology
Volume | Issue number 3 | 7
Pages (from-to) 941-954
Number of pages 14
Organisations
  • Faculty of Science (FNWI) - Van 't Hoff Institute for Molecular Sciences (HIMS)
  • Faculty of Science (FNWI) - Informatics Institute (IVI)
Abstract
Cardiolipin, the mitochondria marker lipid, is crucially involved in stabilizing the inner mitochondrial membrane and is vital for the activity of mitochondrial proteins and protein complexes. Directly targeting cardiolipin by a chemical-biology approach and thereby altering the cellular concentration of “available” cardiolipin eventually allows to systematically study the dependence of cellular processes on cardiolipin availability. In the present study, physics-based coarse-grained free energy calculations allowed us to identify the physical and chemical properties indicative of cardiolipin selectivity and to apply these to screen a compound database for putative cardiolipin-binders. The membrane binding properties of the 22 most promising molecules identified in the in silico approach were screened in vitro, using model membrane systems finally resulting in the identification of a single molecule, CLiB (CardioLipin-Binder). CLiB clearly affects respiration of cardiolipin-containing intact bacterial cells as well as of isolated mitochondria. Thus, the structure and function of mitochondrial membranes and membrane proteins might be (indirectly) targeted and controlled by CLiB for basic research and, potentially, also for therapeutic purposes.
Document type Article
Note With supplementary file.
Language English
Published at https://doi.org/10.1039/d2cb00125j
Other links https://www.scopus.com/pages/publications/85132524936
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d2cb00125j (Final published version)
Supplementary materials
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