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Cardiolipin-Containing Lipid Membranes Attract the Bacterial Cell Division Protein DivIVA
N. Labajová, N. Baranova, M. Jurásek, R. Vácha, M. Loose, I. Barák
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články
Grantová podpora
2/0001/21
Vedecká Grantová Agentúra MŠVVaŠ SR a SAV
APVV-18-0104
Agentúra na Podporu Výskumu a Vývoja
GA20-20152S
Grantová Agentura České Republiky
679239
European Research Council - International
NLK
Free Medical Journals
od 2000
Freely Accessible Science Journals
od 2000
PubMed Central
od 2007
Europe PubMed Central
od 2007
ProQuest Central
od 2000-03-01
Open Access Digital Library
od 2000-01-01
Open Access Digital Library
od 2007-01-01
Health & Medicine (ProQuest)
od 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
od 2000
PubMed
34361115
DOI
10.3390/ijms22158350
Knihovny.cz E-zdroje
- MeSH
- bakteriální proteiny metabolismus MeSH
- buněčná membrána metabolismus MeSH
- Clostridioides difficile růst a vývoj metabolismus MeSH
- kardiolipiny metabolismus MeSH
- membránové lipidy metabolismus MeSH
- proteiny buněčného cyklu metabolismus MeSH
- transport proteinů MeSH
- Publikační typ
- časopisecké články MeSH
DivIVA is a protein initially identified as a spatial regulator of cell division in the model organism Bacillus subtilis, but its homologues are present in many other Gram-positive bacteria, including Clostridia species. Besides its role as topological regulator of the Min system during bacterial cell division, DivIVA is involved in chromosome segregation during sporulation, genetic competence, and cell wall synthesis. DivIVA localizes to regions of high membrane curvature, such as the cell poles and cell division site, where it recruits distinct binding partners. Previously, it was suggested that negative curvature sensing is the main mechanism by which DivIVA binds to these specific regions. Here, we show that Clostridioides difficile DivIVA binds preferably to membranes containing negatively charged phospholipids, especially cardiolipin. Strikingly, we observed that upon binding, DivIVA modifies the lipid distribution and induces changes to lipid bilayers containing cardiolipin. Our observations indicate that DivIVA might play a more complex and so far unknown active role during the formation of the cell division septal membrane.
CEITEC and Faculty of Science Masaryk University Kamenice 5 625 00 Brno Czech Republic
Institute of Molecular Biology SAS Dubravska Cesta 21 845 51 Bratislava Slovakia
Institute of Science and Technology Austria Am Campus 1 3400 Klosterneuburg Austria
Citace poskytuje Crossref.org
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