1. Academic Validation
  2. Sensitive red fluorescent indicators for real-time visualization of potassium ion dynamics in vivo

Sensitive red fluorescent indicators for real-time visualization of potassium ion dynamics in vivo

  • PLoS Biol. 2025 Sep 17;23(9):e3002993. doi: 10.1371/journal.pbio.3002993.
Lina Yang 1 2 3 4 Vishaka Pathiranage 5 Shihao Zhou 2 3 4 Xiaoting Sun 2 3 4 Hanbin Zhang 2 3 4 Cuixin Lai 2 3 4 Chenlei Gu 2 3 4 Fedor V Subach 6 Mikhail Drobizhev 7 Alice R Walker 5 Kiryl D Piatkevich 2 3 4
Affiliations

Affiliations

  • 1 School of Life Sciences, Fudan University, Shanghai, China.
  • 2 School of Life Sciences, Westlake University, Hangzhou, Zhejiang, China.
  • 3 Westlake Laboratory of Life Sciences and Biomedicine, Hangzhou, Zhejiang, China.
  • 4 Institute of Basic Medical Sciences, Westlake Institute for Advance Study, Hangzhou, Zhejiang, China.
  • 5 Department of Chemistry, Wayne State University, Detroit, Michigan, United States of America.
  • 6 Complex of NBICS Technologies, National Research Center "Kurchatov Institute", Moscow, Russia.
  • 7 Department of Microbiology and Cell Biology, Montana State University, Bozeman, Montana, United States of America.
Abstract

Potassium ion (K+) dynamics are vital for various biological processes. However, the limited availability of detection tools for tracking intracellular and extracellular K+ has impeded a comprehensive understanding of the physiological roles of K+ in intact biological systems. In this study, we developed two novel red genetically encoded potassium indicators (RGEPOs), RGEPO1 and RGEPO2, through a combination of directed evolution in Escherichia coli and subsequent optimization in mammalian cells. RGEPO1, targeted to the extracellular membrane, and RGEPO2, localized in the cytoplasm, exhibited positive K+-specific fluorescence response with affinities of 2.4 and 43.3 mM in HEK293FT cells, respectively. We employed RGEPOs for real-time monitoring of subsecond K+ dynamics in cultured neurons, astrocytes, acute brain slices, and the awake mouse in both intracellular and extracellular environments. Using RGEPOs, we were able, for the first time, to visualize intracellular and extracellular potassium transients during seizures in the brains of awake mice. Furthermore, molecular dynamics simulations provided new insights into the potassium-binding mechanisms of RGEPO1 and RGEPO2, revealing distinct K+-binding pockets and structural features. Thus, RGEPOs represent a significant advancement in potassium imaging, providing enhanced tools for real-time visualization of K+ dynamics in various cell types and cellular environments.

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