Phytohormone Spatial Profiling
Phytohormone Spatial Profiling
Overview of Phytohormone Spatial Profiling Technology
The Technical Workflow of MALDI-based Phytohormone Spatial Profiling
Why Choose MetwareBio for Phytohormone Spatial Profiling?
Phytohormone Coverage for Spatial Metabolomics Analysis
| Class | Number | Compound |
| Auxins | 13 | IAA-Glu, OxIAA, IAA-Asp, IAA-Leu, IAA-Val, IAA-Trp, ILA, IA, IAA-Ala, IAA-Phe, ICA, IAA, IBA |
| Gibberellins (GAs) | 11 | GA15, GA19, GA53, GA7, GA9, GA8, GA5, GA6, GA29, GA34, GA12-ald |
| Jasmonates (JAs) | 6 | OPC-4, OPC-6, H2JA, JA, JA-ILE, 12-OH-JA |
| Salicylates | 5 | SA, SAG, Phe, t-CA, 2-Coumarate |
| Abscisic Acid | 1 | ABA |
Note: For cytokinin analysis, please consider our MALDI untargeted spatial metabolomics service.
Plant Hormone Spatial Metabolomics Analysis Workflow
Applications of Plant Hormone Spatial Profiling
Spatial profiling of phytohormones provides direct insight into how localized hormone gradients shape plant growth, organ initiation, vascular differentiation, and reproductive development. By visualizing the in situ distribution of auxins, gibberellins, jasmonates, salicylates, and abscisic acid, researchers can dissect tissue-specific signaling networks underlying root architecture, leaf formation, meristem activity, seed development, and fruit maturation. This spatially resolved approach is particularly valuable for decoding hormone crosstalk in developmental biology and functional plant research.
Phytohormones are central regulators of plant responses to drought, salinity, temperature extremes, wounding, and pathogen challenge. Spatial metabolomics enables precise mapping of hormone accumulation and redistribution within stressed tissues, revealing localized defense activation, stress signaling hubs, and adaptive metabolic reprogramming. This approach supports mechanistic studies of ABA-mediated abiotic stress tolerance, JA- and SA-associated defense pathways, and multi-hormone coordination in resilience phenotypes, making it highly relevant for plant stress physiology and crop adaptation research.
The spatial behavior of phytohormones is critical for understanding how plants perceive and respond to microbes and environmental cues. Spatial phytohormone analysis can uncover where immune-related hormones are produced, transported, and accumulated during infection or environmental perturbation, providing a refined view of defense signaling and local–systemic communication. These data support research on host–pathogen interactions, induced resistance, wound signaling, and rhizosphere-associated responses, helping identify molecular mechanisms that govern plant health and environmental adaptation.
Phytohormone spatial profiling offers a powerful tool for linking molecular phenotypes to agronomic traits in crops. By comparing hormone localization patterns across genotypes, treatments, developmental stages, or engineered lines, researchers can identify regulatory hotspots associated with growth vigor, stress tolerance, yield formation, and tissue-specific traits. The technology is well suited for functional genomics, mutant characterization, trait validation, and breeding research, providing spatially resolved molecular evidence to accelerate crop improvement and precision plant science.
Validated Expertise in Phytohormone Spatial Metabolomics
Number of Metabolites Mapped Across Various Plant Tissues by MALDI-based Phytohormone Spatial Profiling
Sample Requirements & Submission Guidelines for Phytohormone MSI
- Embedding Medium: CMC is recommended for optimal tissue support during sectioning.
- Tissue Cross-section Size: 1.5 × 1.5 mm (min) – 50 × 30 mm (max)
- Tissue Height: 2 mm (min) – 25 mm (max)
- Storage & Shipment: Store samples in a frozen tissue storage box and ship on dry ice to maintain sample integrity.
- Slide Type: ITO-coated slides are required for MALDI-MSI analysis.
- Maximum Scanning Area: 65 × 40 mm
- Section Thickness: 8–50 µm
- Storage & Shipment: Store sections in a slide box and ship on dry ice.
FAQs about Phytohormone Spatial Profiling
Our Phytohormone Spatial Profiling service is applicable to a wide range of plant tissues, including fruits, leaves, roots, seeds, stems, and flowers. Fresh-frozen tissue blocks or tissue sections are recommended as sample submission formats to best preserve metabolite integrity and spatial distribution for MALDI-MSI analysis.
For optimal spatial metabolomics results, plant samples should be fresh-frozen as quickly as possible after collection to preserve native metabolite distributions. Tissue blocks are typically embedded in CMC, sectioned at an appropriate thickness, mounted on ITO-coated slides, and stored or shipped on dry ice.
This service is performed on the Bruker timsTOF fleX platform using MALDI-based mass spectrometry imaging (MALDI-MSI). Combined with optimized sample preparation and derivatization strategies, the platform enables sensitive spatial visualization of trace-level phytohormones in plant tissues.
Our workflow supports the spatial detection of 36 phytohormones across five major classes: Auxins, Gibberellins (GAs), Jasmonates (JAs), Salicylates, and Abscisic Acid (ABA). This coverage supports research on plant hormone signaling, tissue-specific regulation, and stress responses.
The optimal spatial resolution depends on your research goal, tissue structure, and target distribution pattern. Higher resolution is more suitable for small or heterogeneous tissue regions, while moderate resolution is often sufficient for broader tissue-level profiling. Our team can recommend an appropriate resolution based on your sample type and project objectives.
Next-Generation Omics Solutions:
Proteomics & Metabolomics
Ready to get started? Submit your inquiry or contact us at support-global@metwarebio.com.