Nature Communications (Oct 2023)

Lactate biosensors for spectrally and spatially multiplexed fluorescence imaging

  • Yusuke Nasu,
  • Abhi Aggarwal,
  • Giang N. T. Le,
  • Camilla Trang Vo,
  • Yuki Kambe,
  • Xinxing Wang,
  • Felix R. M. Beinlich,
  • Ashley Bomin Lee,
  • Tina R. Ram,
  • Fangying Wang,
  • Kelsea A. Gorzo,
  • Yuki Kamijo,
  • Marc Boisvert,
  • Suguru Nishinami,
  • Genki Kawamura,
  • Takeaki Ozawa,
  • Hirofumi Toda,
  • Grant R. Gordon,
  • Shaoyu Ge,
  • Hajime Hirase,
  • Maiken Nedergaard,
  • Marie-Eve Paquet,
  • Mikhail Drobizhev,
  • Kaspar Podgorski,
  • Robert E. Campbell

DOI
https://doi.org/10.1038/s41467-023-42230-5
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 17

Abstract

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Abstract l-Lactate is increasingly appreciated as a key metabolite and signaling molecule in mammals. However, investigations of the inter- and intra-cellular dynamics of l-lactate are currently hampered by the limited selection and performance of l-lactate-specific genetically encoded biosensors. Here we now report a spectrally and functionally orthogonal pair of high-performance genetically encoded biosensors: a green fluorescent extracellular l-lactate biosensor, designated eLACCO2.1, and a red fluorescent intracellular l-lactate biosensor, designated R-iLACCO1. eLACCO2.1 exhibits excellent membrane localization and robust fluorescence response. To the best of our knowledge, R-iLACCO1 and its affinity variants exhibit larger fluorescence responses than any previously reported intracellular l-lactate biosensor. We demonstrate spectrally and spatially multiplexed imaging of l-lactate dynamics by coexpression of eLACCO2.1 and R-iLACCO1 in cultured cells, and in vivo imaging of extracellular and intracellular l-lactate dynamics in mice.