Spatial Post-Translational Modification Mapping Service

Our Spatial Post-Translational Modification (PTM) Mapping service provides a high-resolution window into the true functional state of the proteome. Moving beyond standard protein abundance, we enable you to visualize how proteins are modified (e.g., phosphorylation, acetylation) and exactly where active signaling occurs within the complex tissue architecture. By mapping these dynamic functional states in situ, we empower drug developers and translational researchers to elucidate drug mechanisms of action, validate novel therapeutic targets, and discover functional biomarkers with unprecedented spatial context.

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  • What is
  • Workflow
  • Platform
  • Applications
  • Why choose
  • FAQs
  • Sample preparation

What is Spatial PTM Mapping?

Post-translational modifications (PTMs) are the "on/off" switches of cellular function. While genomics tells you the blueprint and proteomics tells you the machinery, PTM mapping tells you the activity.

Spatial PTM Mapping utilizes advanced technologies—such as MALDI-MSI (Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry Imaging) or Antibody-based Multiplexing—to detect specific chemical changes on proteins across a 2D or 3D tissue landscape. This allows for the visualization of localized signaling pathways within tumors, brain regions, or inflamed tissues.

Workflow

From Sample to Insight. We provide a seamless, end-to-end pipeline designed to ensure data integrity and biological relevance.

Spatial PTM Mapping workflow

Our Technology Platform

We utilize a multi-modal approach to suit diverse research needs:

  • MALDI-TOF/TOF & FT-ICR MSI: For label-free, discovery-based mapping of glycans and small molecule modifications with high mass accuracy.
  • High-Plex Spatial Proteomics: Using DNA-barcoded antibodies to detect dozens of specific phosphorylated proteins simultaneously at sub-cellular resolution.
  • Advanced Image Fusion: Proprietary software to overlay molecular heatmaps onto high-resolution histological images.

Key Applications

  • Oncology: Identifying "active" signaling zones in the tumor microenvironment to predict drug resistance.
  • Neuroscience: Mapping protein phosphorylation patterns in neurodegenerative diseases like Alzheimer's or Parkinson's.
  • Drug Development: Visualizing the spatial distribution of a drug's effect on target protein modification (Pharmacodynamics).
  • Immunology: Tracking the activation state of immune cells as they infiltrate specific tissue niches.

Why Choose Us?

  • Unmatched Sensitivity: Our platform detects low-abundance PTMs that are often missed by standard imaging techniques.
  • Expert Integration: We don't just provide raw data; we provide biological context, linking molecular shifts to morphological features.
  • Customization: We develop bespoke protocols for "difficult" modifications or unique tissue types.
  • Validated Accuracy: Every project includes rigorous internal standards to ensure spatial and chemical fidelity.

FAQs

What is the spatial resolution of this service?

A: Depending on the platform, we offer resolution ranging from 5 μm (sub-cellular) to 50 μm (regional), tailored to your tissue size and goals.

Can you map multiple PTMs at once?

A: Yes. Through multiplexed imaging or sequential MSI runs, we can correlate different modifications (e.g., Glycosylation and Phosphorylation) on the same or adjacent sections.

How do you ensure the PTMs don't degrade during processing?

A: We utilize specialized protease and phosphatase inhibitors during sample prep and maintain strict cold-chain protocols for fresh-frozen materials.

Learn about other Q&A.

Sample Preparation Guidelines

To ensure the highest data quality, please adhere to the following:

Tissue Types: We accept Fresh Frozen (FF), Optimal Cutting Temperature (OCT) embedded, or FFPE tissues. For MALDI-MSI projects, please avoid OCT compound as it interferes with mass spectral ionization. Use CMC (Carboxymethyl Cellulose) or Gelatin embedding instead. OCT is accepted only for Antibody-based/Immunofluorescence projects.Thickness:

Storage: Frozen samples must be shipped on dry ice and stored at -80°C to prevent PTM degradation (especially for phosphorylation).

Slides: Use conductive slides (ITO) for MSI or adhesive slides for multiplexed imaging as specified during consultation.

NOTE: Please consult with our technical team prior to sample preparation to obtain a detailed protocol.

* For Research Use Only. Not for use in diagnostic procedures.
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