4.4 Article

Spot Variation Fluorescence Correlation Spectroscopy for Analysis of Molecular Diffusion at the Plasma Membrane of Living Cells

Journal

JOVE-JOURNAL OF VISUALIZED EXPERIMENTS
Volume -, Issue 165, Pages -

Publisher

JOURNAL OF VISUALIZED EXPERIMENTS
DOI: 10.3791/61823

Keywords

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Funding

  1. CNRS
  2. Inserm
  3. Aix-Marseille University
  4. French National Research Agency [ANR-17-CE15-0032-01, ANR-18-CE15-0021-02]
  5. French Investissement d'Avenir [ANR-10-INBS-04 France-BioImaging, ANR-11-LABX-054 labex INFORM]
  6. National Science Centre of Poland (NCN) [2016/21/D/NZ1/00285]
  7. French Government
  8. Embassy of France in Poland
  9. Polish Ministry of Development [CBR POIR.02.01.00-00-0159/15-00/19]
  10. National Center for Research and Development [Innochem POIR.01.02.00-00-0064/17]
  11. National Science Center of Poland (NCN) [2016/21/B/NZ3/00343]
  12. Wroclaw Biotechnology Center (KNOW)
  13. Agence Nationale de la Recherche (ANR) [ANR-17-CE15-0032, ANR-18-CE15-0021] Funding Source: Agence Nationale de la Recherche (ANR)

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Dynamic biological processes in living cells, including those associated with plasma membrane organization, occur on various spatial and temporal scales, ranging from nanometers to micrometers and microseconds to minutes, respectively. Such a broad range of biological processes challenges conventional microscopy approaches. Here, we detail the procedure for implementing spot variation Fluorescence Correlation Spectroscopy (svFCS) measurements using a classical fluorescence microscope that has been customized. The protocol includes a specific performance check of the svFCS setup and the guidelines for molecular diffusion measurements by svFCS on the plasma membrane of living cells under physiological conditions. Additionally, we provide a procedure for disrupting plasma membrane raft nanodomains by cholesterol oxidase treatment and demonstrate how these changes in the lateral organization of the plasma membrane might be revealed by svFCS analysis. In conclusion, this fluorescence-based method can provide unprecedented details on the lateral organization of the plasma membrane with the appropriate spatial and temporal resolution.

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