Genetically encoded biosensor for fluorescence lifetime imaging of PTEN dynamics in the intact brain

The phosphatase and tensin homolog (PTEN) is a vital protein that maintains an inhibitory brake for cellular proliferation and growth. Accordingly, PTEN loss-of-function mutations are associated with a broad spectrum of human pathologies. Despite its importance, there is currently no method to directly monitor PTEN activity with cellular specificity within intact biological systems. Here we describe the development of a FRET-based biosensor using PTEN conformation as a proxy for the PTEN activity state, for two-photon fluorescence lifetime imaging microscopy. We identify a point mutation that allows the monitoring of PTEN activity with minimal interference to endogenous PTEN signaling. We demonstrate imaging of PTEN activity in cell lines, intact Caenorhabditis elegans and in the mouse brain. Finally, we develop a red-shifted sensor variant that allows us to identify cell-type-specific PTEN activity in excitatory and inhibitory cortical cells. In summary, our approach enables dynamic imaging of PTEN activity in vivo with unprecedented spatial and temporal resolution.

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Publication Details

Journal
Nature Methods
Published
2025-02-20
DOI
https://doi.org/10.1038/s41592-025-02610-9
Citations
15
Primary Topic
PI3K/AKT/mTOR signaling in cancer
Type
article
Field-Weighted Citation Impact
12.09
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article

Genetically encoded biosensor for fluorescence lifetime imaging of PTEN dynamics in the intact brain

Matan Gabay, Tal Laviv, Anat Nitzan, Luca Ravotto et al.
15 citations
Nature Methods
PI3K/AKT/mTOR signaling in cancer
12.09
article

Genetically encoded biosensor for fluorescence lifetime imaging of PTEN dynamics in the intact brain

Matan Gabay, Tal Laviv, Anat Nitzan, Luca Ravotto, Maayan Gal, Ronen Zaidel‐Bar, Sharbel Eid, Britta J. Eickholt, Tomer Kagan, Nikol Malchenko, Maya Maman, Y. Levi, Aasha Meenakshisundaram
article en
15 citations

Abstract

The phosphatase and tensin homolog (PTEN) is a vital protein that maintains an inhibitory brake for cellular proliferation and growth. Accordingly, PTEN loss-of-function mutations are associated with a broad spectrum of human pathologies. Despite its importance, there is currently no method to directly monitor PTEN activity with cellular specificity within intact biological systems. Here we describe the development of a FRET-based biosensor using PTEN conformation as a proxy for the PTEN activity state, for two-photon fluorescence lifetime imaging microscopy. We identify a point mutation that allows the monitoring of PTEN activity with minimal interference to endogenous PTEN signaling. We demonstrate imaging of PTEN activity in cell lines, intact Caenorhabditis elegans and in the mouse brain. Finally, we develop a red-shifted sensor variant that allows us to identify cell-type-specific PTEN activity in excitatory and inhibitory cortical cells. In summary, our approach enables dynamic imaging of PTEN activity in vivo with unprecedented spatial and temporal resolution.

Nature MethodsVol. 22(4)
Tel Aviv University (IL), University of Zurich (CH), Charité - Universitätsmedizin Berlin (DE)
Openalex Percentile: Top 1%
PI3K/AKT/mTOR signaling in cancer
12.09
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