Dynamic imaging of homo-FRET in live cells by fluorescence anisotropy microscopy

Methods Enzymol. 2012:505:291-327. doi: 10.1016/B978-0-12-388448-0.00024-3.


Multiple lipid and protein components of the plasma membrane of a living cell are organized, both compositionally and functionally, at different spatial and temporal scales. For instance, Rab protein domains in membranes the clathrin-coated pit, or the immunological synapse are exquisite examples of functional compartmentalization in cell membranes. These assemblies consist in part of nanoscale complexes of lipids and proteins and are necessary to facilitate some specific sorting and signaling functions. It is evident that cellular functions require a regulated spatiotemporal organization of components at the nanoscale, often comprising of countable number of molecular species. Here, we describe multiple homo-FRET-based imaging methods that provide information about nanoscale interactions between fluorescently tagged molecules in live cells, at optically resolved spatial resolution.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Membrane / metabolism
  • Cell Tracking / methods*
  • Drosophila / cytology
  • Fluorescence Polarization / instrumentation
  • Fluorescence Polarization / methods
  • Fluorescence Resonance Energy Transfer / methods*
  • Green Fluorescent Proteins*
  • Image Processing, Computer-Assisted
  • Lipid Metabolism
  • Microscopy, Confocal / instrumentation
  • Microscopy, Confocal / methods*
  • Microscopy, Fluorescence / methods*


  • Green Fluorescent Proteins