Unverified paper record
Fluorescence Lifetime Imaging in Plants: Practical guidelines for multiplexing, label-free imaging and data analysis
bioRxiv · 11 Jun 2026 · 10.64898/2026.06.11.731528
Abstract
ABSTRACT Fluorescence Lifetime Imaging Microscopy (FLIM) is becoming a key technique for live-cell multiplexing and label-free detection of endogenous fluorescence in animal systems. Its potential in plant biology, however remains largely unexploited, despite its integration into a number of commercial microscopy setups. Here, we build a systematic, subcellular FLIM reference library for a panel of genetically-encoded fluorophores. Lifetime imaging of different fluorescent reporters targeted to distinct organelles (nucleus, plasma membrane, endoplasmic reticulum, etc.) and subsequent analysis of the decay curves using different modes allowed us to simultaneously discriminate up to four spectrally overlapping fluorophores solely by lifetime differences in specific subcellular compartments. Remarkably, fluorophores with lifetimes differing by as little as 0.1 ns can be reliably discriminated using one of these modes, namely Phasor-based analysis. Moreover, we show that the same fluorophores exhibit compartment-specific lifetime shifts, enabling Phasor separation of identical tags residing in different organelles. Finally, we extended the Phasor approach to label-free imaging of endogenous plant fluorescence. Together, these results establish FLIM-Phasor as a versatile, multiplex-capable tool for plant cell biology, opening new avenues for imaging strategies that yield higher content information at both cellular and tissue-level resolution.
Plant phenotyping relevance
植物細胞・組織の蛍光状態を取得・解析するFLIM-Phasor法を体系的に構築・検証し、マルチプレックスおよびラベルフリー植物蛍光イメージングへの応用を示した、方法中心の研究である。
abstractHere, we build a systematic, subcellular FLIM reference library for a panel of genetically-encoded fluorophores.
abstractRemarkably, fluorophores with lifetimes differing by as little as 0.1 ns can be reliably discriminated using one of these modes, namely Phasor-based analysis.
abstractTogether, these results establish FLIM-Phasor as a versatile, multiplex-capable tool for plant cell biology, opening new avenues for imaging strategies that yield higher content information at both cellular and tissue-level resolution.
Code and data availability
The paper reports FLIM-Phasor plant imaging data but provides no public repository, dataset, image deposit, or author code URL. Supplementary data are referenced without a link, and the URLs present (fpbase, PhasorPy, bids colourmap) are generic third-party tools, not paper-specific assets.
No evidence-backed public reproduction asset is currently recorded.
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