Identification of key phospholipids that bind and activate atypical PKCs

PKCζ and PKCι/λ form the atypical protein kinase C subgroup, characterised by a lack of regulation by calcium and the neutral lipid diacylglycerol. To better understand the regulation of these kinases, we systematically explored their interactions with various purified phospholipids using the lipid...

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Detalles Bibliográficos
Autores: Velnati, Suresh, Centonze, Sara, Girivetto, Federico, Capello, Daniela, Biondi, Ricardo Miguel, Bertoni, Alessandra, Cantello, Roberto, Ragnoli, Beatrice, Malerba, Mario, Graziani, Andrea, Baldanzi, Gianluca
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2021
País:Argentina
Institución:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositorio:CONICET Digital (CONICET)
Idioma:inglés
OAI Identifier:oai:ri.conicet.gov.ar:11336/184896
Acceso en línea:http://hdl.handle.net/11336/184896
Access Level:acceso abierto
Palabra clave:KINASE REGULATION
LIPID SIGNALLING
LIPID-PROTEIN INTERACTION
MEMBRANE
PHOSPHATIDYLINOSITOLS
https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
Descripción
Sumario:PKCζ and PKCι/λ form the atypical protein kinase C subgroup, characterised by a lack of regulation by calcium and the neutral lipid diacylglycerol. To better understand the regulation of these kinases, we systematically explored their interactions with various purified phospholipids using the lipid overlay assays, followed by kinase activity assays to evaluate the lipid effects on their enzymatic activity. We observed that both PKCζ and PKCι interact with phosphatidic acid and phos-phatidylserine. Conversely, PKCι is unique in binding also to phosphatidylinositol-monophosphates (e.g., phosphatidylinositol 3-phosphate, 4-phosphate, and 5-phosphate). Moreover, we observed that phosphatidylinositol 4-phosphate specifically activates PKCι, while both isoforms are responsive to phosphatidic acid and phosphatidylserine. Overall, our results suggest that atypical Protein kinase C (PKC) localisation and activity are regulated by membrane lipids distinct from those involved in con-ventional PKCs and unveil a specific regulation of PKCι by phosphatidylinositol-monophosphates.