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The interaction of the ribotoxin α-sarcin with complex model lipid vesicles.
García-Montoya, Carmen; García-Linares, Sara; Heras-Márquez, Diego; Majnik, Manca; Laxalde-Fernández, Diego; Amigot-Sánchez, Rafael; Martínez-Del-Pozo, Álvaro; Palacios-Ortega, Juan.
Afiliación
  • García-Montoya C; Departamento de Bioquímica y Biología Molecular, Universidad Complutense, Madrid, Spain.
  • García-Linares S; Departamento de Bioquímica y Biología Molecular, Universidad Complutense, Madrid, Spain.
  • Heras-Márquez D; Departamento de Bioquímica y Biología Molecular, Universidad Complutense, Madrid, Spain.
  • Majnik M; Departamento de Bioquímica y Biología Molecular, Universidad Complutense, Madrid, Spain.
  • Laxalde-Fernández D; Departamento de Bioquímica y Biología Molecular, Universidad Complutense, Madrid, Spain.
  • Amigot-Sánchez R; Departamento de Bioquímica y Biología Molecular, Universidad Complutense, Madrid, Spain.
  • Martínez-Del-Pozo Á; Departamento de Bioquímica y Biología Molecular, Universidad Complutense, Madrid, Spain.
  • Palacios-Ortega J; Departamento de Bioquímica y Biología Molecular, Universidad Complutense, Madrid, Spain; Biochemistry, Faculty of Science and Engineering, Åbo Akademi University, Turku, Finland. Electronic address: juan.palaciosb1a@gmail.com.
Arch Biochem Biophys ; 751: 109836, 2024 01.
Article en En | MEDLINE | ID: mdl-38000493
Fungal ribotoxins are extracellular RNases that inactivate ribosomes by cleaving a single phosphodiester bond at the universally conserved sarcin-ricin loop of the large rRNA. However, to reach the ribosomes, they need to cross the plasma membrane. It is there where these toxins show their cellular specificity, being especially active against tumoral or virus-infected cells. Previous studies have shown that fungal ribotoxins interact with negatively charged membranes, typically containing phosphatidylserine or phosphatidylglycerol. This ability is rooted on their long, non-structured, positively charged loops, and its N-terminal ß-hairpin. However, its effect on complex lipid mixtures, including sphingophospholipids or cholesterol, remains poorly studied. Here, wild-type α-sarcin was used to evaluate its interaction with a variety of membranes not assayed before, which resemble much more closely mammalian cell membranes. The results confirm that α-sarcin is particularly sensitive to charge density on the vesicle surface. Its ability to induce vesicle aggregation is strongly influenced by both the lipid headgroup and the degree of saturation of the fatty acid chains. Acyl chain length is indeed particularly important for lipid mixing. Finally, cholesterol plays an important role in diluting the concentration of available negative charges and modulates the ability of α-sarcin to cross the membrane.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Fúngicas / Endorribonucleasas Idioma: En Revista: Arch Biochem Biophys Año: 2024 Tipo del documento: Article País de afiliación: España Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Fúngicas / Endorribonucleasas Idioma: En Revista: Arch Biochem Biophys Año: 2024 Tipo del documento: Article País de afiliación: España Pais de publicación: Estados Unidos