Your browser doesn't support javascript.
loading
PI(4,5)P2 Clustering and Its Impact on Biological Functions.
Wen, Yi; Vogt, Volker M; Feigenson, Gerald W.
Afiliación
  • Wen Y; Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York 14850, USA; email: yw592@cornell.edu, vmv1@cornell.edu, gwf3@cornell.edu.
  • Vogt VM; Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York 14850, USA; email: yw592@cornell.edu, vmv1@cornell.edu, gwf3@cornell.edu.
  • Feigenson GW; Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York 14850, USA; email: yw592@cornell.edu, vmv1@cornell.edu, gwf3@cornell.edu.
Annu Rev Biochem ; 90: 681-707, 2021 06 20.
Article en En | MEDLINE | ID: mdl-33441034
ABSTRACT
Located at the inner leaflet of the plasma membrane (PM), phosphatidyl-inositol 4,5-bisphosphate [PI(4,5)P2] composes only 1-2 mol% of total PM lipids. With its synthesis and turnover both spatially and temporally regulated, PI(4,5)P2 recruits and interacts with hundreds of cellular proteins to support a broad spectrum of cellular functions. Several factors contribute to the versatile and dynamic distribution of PI(4,5)P2 in membranes. Physiological multivalent cations such as Ca2+ and Mg2+ can bridge between PI(4,5)P2 headgroups, forming nanoscopic PI(4,5)P2-cation clusters. The distinct lipid environment surrounding PI(4,5)P2 affects the degree of PI(4,5)P2 clustering. In addition, diverse cellular proteins interacting with PI(4,5)P2 can further regulate PI(4,5)P2 lateral distribution and accessibility. This review summarizes the current understanding of PI(4,5)P2 behavior in both cells and model membranes, with emphasis on both multivalent cation- and protein-induced PI(4,5)P2 clustering. Understanding the nature of spatially separated pools of PI(4,5)P2 is fundamental to cell biology.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Replicación Viral / Fosfatidilinositol 4,5-Difosfato / Interacciones Huésped-Patógeno Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Annu Rev Biochem Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Replicación Viral / Fosfatidilinositol 4,5-Difosfato / Interacciones Huésped-Patógeno Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Annu Rev Biochem Año: 2021 Tipo del documento: Article