Analysis of Nanosensor-Reported Waveforms for Plant Wounding

Using nanosensors in living plants allows the real-time detection of internal reactive oxygen species (e.g., hydrogen peroxide) signaling in response to environmental stressors. The time-dependent pulse of hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) constitutes a <i>signaling waveform</i>; however, standardized methods of extracting and analyzing such waveforms quantitatively remain elusive. Here, we develop a reference-less framework to extract stress-induced H<sub>2</sub>O<sub>2</sub> waveforms <i>in</i> <i>planta</i> directly from active nanosensors for the first time. We show that waveforms extracted for 3-week-old spinach across different experimental configurations, including 2D nIR imaging and 1D spectroscopy, are identical. Using this standardized approach, we systematically validate an analytical waveform model based on H<sub>2</sub>O<sub>2</sub> reaction-diffusion transport with a large waveform data set and extract the wave velocities and propagation rate constants from different waveforms. A wave-velocity-rate constant map is created for comparative studies. Results suggest that nanosensors can identify distinct waveforms associated with specific plant stressors with the proposed framework, providing opportunities for new diagnostic tools.

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Publication Details

Journal
Nano Letters
Published
2026-03-28
DOI
https://doi.org/10.1021/acs.nanolett.5c06366
Primary Topic
Plant Stress Responses and Tolerance
Type
article
Field-Weighted Citation Impact
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article

Analysis of Nanosensor-Reported Waveforms for Plant Wounding

Gajendra Singh, Mervin Chun‐Yi Ang, Thomas Porter, Niying Chua et al.
Nano Letters
Plant Stress Responses and Tolerance
article

Analysis of Nanosensor-Reported Waveforms for Plant Wounding

Gajendra Singh, Mervin Chun‐Yi Ang, Thomas Porter, Niying Chua, Duc Thinh Khong, Gabriel Sánchez-Velázquez, Rajeev J. Ram, Rajani Sarojam, Cody L. Ritt, Michael S. Strano, Yile Jiang
article en

Abstract

Using nanosensors in living plants allows the real-time detection of internal reactive oxygen species (e.g., hydrogen peroxide) signaling in response to environmental stressors. The time-dependent pulse of hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) constitutes a <i>signaling waveform</i>; however, standardized methods of extracting and analyzing such waveforms quantitatively remain elusive. Here, we develop a reference-less framework to extract stress-induced H<sub>2</sub>O<sub>2</sub> waveforms <i>in</i> <i>planta</i> directly from active nanosensors for the first time. We show that waveforms extracted for 3-week-old spinach across different experimental configurations, including 2D nIR imaging and 1D spectroscopy, are identical. Using this standardized approach, we systematically validate an analytical waveform model based on H<sub>2</sub>O<sub>2</sub> reaction-diffusion transport with a large waveform data set and extract the wave velocities and propagation rate constants from different waveforms. A wave-velocity-rate constant map is created for comparative studies. Results suggest that nanosensors can identify distinct waveforms associated with specific plant stressors with the proposed framework, providing opportunities for new diagnostic tools.

Nano Letters
Temasek Life Sciences Laboratory (SG), Nanyang Technological University (SG), University of Colorado Boulder (US), University of Colorado System (US), Singapore-MIT Alliance for Research and Technology (SG), Massachusetts Institute of Technology (US)
Openalex Percentile: Top 4%
Plant Stress Responses and Tolerance
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