Video-rate label-free molecular mapping in living plant tissue with a deployable optical encoder

Abstract Living tissues contain dynamic biochemical information that is difficult to capture with conventional hyperspectral microscopes because sequential spectral acquisition is poorly matched to in vivo molecular processes that evolve during measurement. Here we introduce a task-specific optical encoding framework for video-rate molecular inference in living plant tissue. The system integrates a passive spectral encoder, implemented here as a low-angle scattering LDPE layer, into a 22-mm miniaturized probe and learns a supervised mapping from ultraviolet-excited autofluorescence measurements to biomolecular abundance maps. Unlike conventional pipelines that first reconstruct hyperspectral datacubes and then perform spectral unmixing, the deployed system directly estimates endogenous molecular contrast associated primarily with lignin and chlorophyll in poplar tissue, with additional suberin-associated contrast evaluated in suberin-rich tissue. This reframing makes the measurement task biomolecular inference rather than spectral reconstruction, enabling biochemical mapping under low-photon autofluorescence conditions while reducing data burden and computational latency. In living poplar stems, the platform captures autofluorescence-derived videos of embolism propagation and wound-induced biochemical remodeling, dynamic processes for which sequential spectral acquisition can introduce temporal mixing because the molecular contrast evolves during the scan itself. The system also resolves genotype-dependent reductions in lignin-associated autofluorescence in engineered poplar lines. Direct molecular inference improves biomolecular estimation relative to a reconstruction-based pipeline, while probabilistic decoding provides uncertainty estimates. These results show that compact passive spectral encoding, when optimized for biological inference rather than datacube recovery, enables deployable, label-free molecular videography of living plant tissue dynamics after task-specific calibration.