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Detection of Small GTPase Prenylation and GTP Binding Using Membrane Fractionation and GTPase-linked Immunosorbent Assay

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  • Additional Information
    • Contributors:
      Centre de biophysique moléculaire (CBM); Université d'Orléans (UO)-Université de Tours (UT)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS); Le Studium Loire Valley Institute for Advanced Studies, 45000 Orléans, France; This project has been supported by LE STUDIUM Loire Valley Institute for Advanced Studies, Orléans & Tours, France with funding from the European Union's Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement No. 665790
    • Publication Information:
      HAL CCSD
      JoVE
    • Publication Date:
      2018
    • Collection:
      Université d'Orléans: HAL
    • Abstract:
      International audience ; The Rho GTPase family belongs to the Ras superfamily and includes approximately 20 members in humans. Rho GTPases are important in the regulation of diverse cellular functions, including cytoskeletal dynamics, cell motility, cell polarity, axonal guidance, vesicular trafficking, and cell cycle control. Changes in Rho GTPase signaling play an essential regulatory role in many pathological conditions, such as cancer, central nervous system diseases, and immune system-dependent diseases. The posttranslational modification of Rho GTPases (i.e., prenylation by mevalonate pathway intermediates) and GTP binding are key factors which affect the activation of this protein. In this paper, two essential and simple methods are provided to detect a broad range of Rho GTPase prenylation and GTP binding activities. Details of the technical procedures that have been used are explained step by step in this manuscript.
    • Relation:
      hal-02506767; https://hal.science/hal-02506767; https://hal.science/hal-02506767/document; https://hal.science/hal-02506767/file/Publication%206%20-%20Los.pdf
    • Accession Number:
      10.3791/57646
    • Online Access:
      https://hal.science/hal-02506767
      https://hal.science/hal-02506767/document
      https://hal.science/hal-02506767/file/Publication%206%20-%20Los.pdf
      https://doi.org/10.3791/57646
    • Rights:
      info:eu-repo/semantics/OpenAccess
    • Accession Number:
      edsbas.15681484