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---name: aav-vector-design-agent description: AI-powered adeno-associated virus (AAV) vector design for gene therapy including capsid engineering, promoter selection, and tropism optimization. license: MIT metadata: author: AI Group version: "1.0.0" created: "2026-01-19" compatibility:
Full skill instructions
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The AAV Vector Design Agent provides AI-driven design of adeno-associated virus vectors for gene therapy applications. It covers capsid selection and engineering, promoter/enhancer design, transgene optimization, and manufacturing considerations.
Capsid Selection: Match AAV serotype to target tissue based on tropism profiles.
Capsid Engineering: Design modified capsids for enhanced transduction or immune evasion.
Promoter Design: Select and optimize tissue-specific or ubiquitous promoters.
Transgene Optimization: Codon optimization and regulatory element design.
Immunogenicity Prediction: Predict NAb binding and T-cell epitopes.
Manufacturing Assessment: Evaluate producibility and purification considerations.
| Serotype | Primary Tropism | Clinical Use |
|---|---|---|
| AAV1 | Muscle, CNS | Glybera (muscle) |
| AAV2 | Broad (liver, muscle) | Luxturna (retina) |
| AAV5 | CNS, liver, retina | Hemgenix (liver) |
| AAV8 | Liver, muscle | Multiple trials |
| AAV9 | CNS, cardiac, liver | Zolgensma (CNS) |
| AAVrh10 | CNS, liver | CNS trials |
| AAVrh74 | Muscle | Elevidys (muscle) |
| AAV-PHP.eB | CNS (mouse) | Research |
Input: Target tissue, therapeutic gene, patient population characteristics.
Capsid Selection: Rank serotypes by tropism profile match.
Capsid Engineering: Design modifications if needed (peptide insertion, point mutations).
Cassette Design: Optimize ITR-to-ITR expression cassette.
Immunogenicity Analysis: Predict NAb prevalence and T-cell epitopes.
Manufacturing Review: Assess production feasibility.
Output: Complete vector design with rationale.
User: "Design an AAV vector for liver-directed gene therapy in hemophilia B with low immunogenicity."
Agent Action:
python3 Skills/Gene_Therapy/AAV_Vector_Design_Agent/aav_designer.py \
--target_tissue liver \
--therapeutic_gene F9 \
--indication hemophilia_b \
--minimize_immunogenicity true \
--nab_escape true \
--promoter liver_specific \
--output aav_design/
5' ITR - [Promoter] - [5' UTR] - [Transgene] - [WPRE] - [PolyA] - 3' ITR
Packaging limit: ~4.7 kb between ITRs
Promoter Options:
| Promoter | Type | Size | Application |
|---|---|---|---|
| CAG | Ubiquitous | 1.7 kb | Strong expression |
| EF1α | Ubiquitous | 1.2 kb | Constitutive |
| LP1 | Liver-specific | 0.5 kb | Hepatocyte targeting |
| hSyn | Neuron-specific | 0.5 kb | CNS applications |
| MCK | Muscle-specific | 0.6 kb | Myopathies |
| CMV | Ubiquitous | 0.6 kb | High initial (silenced) |
Directed Evolution:
Rational Design:
Machine Learning:
Pre-existing NAbs:
| Serotype | NAb Prevalence |
|---|---|
| AAV2 | 30-60% |
| AAV5 | 15-30% |
| AAV8 | 15-25% |
| AAV9 | 20-35% |
Mitigation Strategies:
Tropism Prediction:
Immunogenicity Modeling:
Expression Optimization:
| Factor | Impact | Optimization |
|---|---|---|
| Capsid yield | Production cost | Sequence modifications |
| Empty/full ratio | Potency | Purification method |
| Aggregation | Stability | Formulation |
| DNA packaging | Transgene size | Cassette design |
AI Group - Biomedical AI Platform
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