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High resolution mapping of subcellular refractive index by Fluorescence Lifetime Imaging: A next frontier in quantitative cell science?

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12 Scopus citations

Abstract

Intracellular refractive index (RI) is an essential biophysical parameter, which best represents the mass and the distribution of proteins in the cell interior, including high-density accumulations in membraneless organelles. For RI measurements, a number of sophisticated techniques have been developed; however most of the new approaches are either insufficiently sensitive to intracellular variations of proteins distribution or are not compatible with live cell studies. Here, we outline the fluorescence lifetime imaging (FLIM) strategy for high resolution mapping of subcellular RI. We provide an example of our recent studies in which we utilize FLIM for measurements and monitoring of local RI in the major membraneless organelles within live cultured cells.

Original languageEnglish
Article number032001
JournalMethods and Applications in Fluorescence
Volume8
Issue number3
DOIs
StatePublished - Jul 2020

Keywords

  • FLIM
  • cellular compartmentalization
  • fluorescence lifetime
  • liquid liquid phase separation
  • membraneless organelles
  • proteins condensation
  • refractive index

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