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Methods Mol Biol ; 2009: 297-306, 2019.
Article in English | MEDLINE | ID: mdl-31152412

ABSTRACT

The posttranslational lipid modification of Rho GTPases is important for their proper subcellular localization and signal transduction. Rho GTPases terminate in a CaaX motif, in which the cysteine residue is modified with either a farnesyl or geranylgeranyl isoprenoid. RhoGDI renders Rho GTPases soluble by masking their lipid moieties. We recently identified that the brain-specific splice variant of Cdc42 (bCdc42) containing a noncanonical CCaX motif harbors a dual prenyl-palmitoyl modification that prevents its binding to RhoGDI. This chapter describes a method to analyze RhoGDI extraction of Rho GTPases containing different lipid modifications from membranes using a liposome reconstitution assay and click chemistry.


Subject(s)
Cell Membrane/chemistry , Click Chemistry , Protein Prenylation , cdc42 GTP-Binding Protein , rho-Specific Guanine Nucleotide Dissociation Inhibitors , Amino Acid Motifs , Animals , Sf9 Cells , Spodoptera , cdc42 GTP-Binding Protein/chemistry , cdc42 GTP-Binding Protein/isolation & purification , rho-Specific Guanine Nucleotide Dissociation Inhibitors/chemistry , rho-Specific Guanine Nucleotide Dissociation Inhibitors/isolation & purification
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