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Deep Visual Proteomics Agent

---name: deep-visual-proteomics-agent description: AI-driven integration of cellular imaging, laser microdissection, and ultra-sensitive mass spectrometry for spatially-resolved single-cell proteomics. license: MIT metadata: author: AI Group version: "1.0.0" created: "2026-01-19" compatibility:

SKILL.md

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Deep Visual Proteomics Agent

The Deep Visual Proteomics Agent implements the Deep Visual Proteomics (DVP) workflow that combines AI-driven image analysis of cellular phenotypes with automated laser microdissection and ultra-high-sensitivity mass spectrometry. It links protein abundance to complex cellular or subcellular phenotypes while preserving spatial context.

When to Use This Skill

  • When studying spatially-resolved protein expression in tissue sections.
  • To link single-cell morphological phenotypes to proteome profiles.
  • For identifying cell-type specific protein signatures in heterogeneous tissues.
  • When analyzing subcellular proteome compartmentalization.
  • To discover spatially-restricted biomarkers in tumor microenvironments.

Core Capabilities

  1. AI Image Segmentation: Deep learning models segment cells and identify phenotypes from brightfield, H&E, or immunofluorescence images.

  2. Phenotype Classification: CNN/​transformer classifiers identify cell types, disease states, and morphological abnormalities.

  3. LMD Coordinate Generation: Automated generation of laser microdissection coordinates for cells of interest.

  4. MS Data Integration: Processes MaxQuant/​DIA-NN output to link protein abundances to spatial coordinates.

  5. Spatial Proteome Mapping: Creates spatially-resolved proteome maps linking morphology to molecular profiles.

  6. Biologically-Informed Analysis: Neural networks incorporating pathway knowledge for interpretable biomarker discovery.

DVP Workflow

Tissue Section
     ↓
[AI Image Analysis] → Cell Segmentation → Phenotype Classification
     ↓
[Region Selection] → LMD Coordinates → Automated Microdissection
     ↓
[Sample Processing] → Low-input LC-MS/​MS → Proteome Quantification
     ↓
[Data Integration] → Spatial Proteome Map → Pathway Analysis

Example Usage

User: "Identify tumor vs. stroma cells in this H&E image and generate proteome profiles for each population."

Agent Action:

python3 Skills/​Proteomics/​Deep_Visual_Proteomics_Agent/​dvp_analyzer.py \
    --image tissue_section.tiff \
    --segmentation cellpose \
    --classifier tumor_stroma_cnn \
    --generate_lmd true \
    --ms_data maxquant_output/ \
    --analysis differential \
    --output dvp_results/

Key Components

ComponentTool/​MethodDescription
SegmentationCellpose, StarDistInstance segmentation of cells
ClassificationCustom CNN/​ViTPhenotype assignment
LMD InterfaceLeica LMD7, PALMCoordinate export formats
MS ProcessingMaxQuant, DIA-NNProtein quantification
IntegrationCustom PythonSpatial mapping

Analysis Outputs

  1. Spatial Protein Maps: Protein abundance overlaid on tissue coordinates
  2. Phenotype-Proteome Links: Proteins enriched in specific cell types
  3. Pathway Activation: Spatial patterns of pathway activity
  4. Differential Analysis: Comparison between regions/​phenotypes
  5. Biomarker Candidates: Spatially-restricted markers

Biologically-Informed Neural Networks (BINNs)

The agent implements BINNs that integrate:

  • A priori knowledge of protein-pathway relationships
  • Sparse neural network architecture mirroring biological networks
  • Enhanced interpretability for clinical applications
  • Validated in septic AKI, COVID-19, and ARDS cohorts
Input: Protein abundances
  ↓
Pathway Layer: Proteins → Pathways (sparse connections)
  ↓
Process Layer: Pathways → Biological processes
  ↓
Output: Phenotype classification + pathway importance scores

Prerequisites

  • Python 3.10+
  • PyTorch with vision models
  • Cellpose/​StarDist for segmentation
  • MS data processing tools
  • GPU recommended for image analysis

Related Skills

  • Pathology_AI - For histopathology analysis
  • Proteomics_MS - For standard proteomics workflows
  • Spatial_Transcriptomics - For complementary spatial RNA

Applications

  1. Tumor Heterogeneity: Map proteome across tumor microenvironment regions
  2. Single-Cell Resolution: Proteome profiles of rare cell populations
  3. Disease Mechanisms: Link morphological changes to molecular drivers
  4. Drug Response: Spatial patterns of treatment response

Technical Specifications

Sensitivity: 100-500 cells per sample for robust quantification Throughput: 1,000-5,000 proteins per sample Resolution: Single-cell to ~10-cell resolution Formats: TIFF/​SVS images, MaxQuant/​DIA-NN output

Author

AI Group - Biomedical AI Platform

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