Optogenetic Control for Investigating Subcellular Localization of Fyn Kinase Activity in Single Live Cells

J Mol Biol. 2020 Mar 27;432(7):1901-1909. doi: 10.1016/j.jmb.2020.03.015. Epub 2020 Mar 18.

Abstract

Previous studies with various Src family kinase biosensors showed that the nuclear kinase activities are much suppressed compared to those in the cytosol, suggesting that these kinases are regulated differently in the nucleus and in the cytosol. In this study, using Fyn as an example, we first engineered a Fyn biosensor with a light-inducible nuclear localization signal to demonstrate that the Fyn kinase activity is significantly lower in the nucleus than in the cytosol. To understand how different equilibrium states between Fyn and the corresponding phosphatases are maintained in the cytosol and nucleus, we further engineered a Fyn kinase domain with light-inducible nuclear localization signal. The results revealed that the Fyn kinase can be actively transported into the nucleus upon light activation and upregulate the biosensor signals in the nucleus. Our results suggest that there is limited transport or diffusion of Fyn kinase between the cytosol and nucleus in the cells, which is important for the maintenance of different equilibrium states of Fyn in situ.

Keywords: FRET biosensor; Fyn kinase; LINuS; light-inducible kinase; live cell imaging.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biosensing Techniques / methods*
  • Cell Nucleus / metabolism*
  • Cells, Cultured
  • Cytosol / metabolism*
  • Fibroblasts / cytology
  • Fibroblasts / metabolism
  • HEK293 Cells
  • Humans
  • Nuclear Localization Signals
  • Optogenetics*
  • Protein Transport
  • Proto-Oncogene Proteins c-fyn / metabolism*
  • Subcellular Fractions / metabolism*

Substances

  • Nuclear Localization Signals
  • Proto-Oncogene Proteins c-fyn