install
source · Clone the upstream repo
git clone https://github.com/majiayu000/claude-skill-registry
Claude Code · Install into ~/.claude/skills/
T=$(mktemp -d) && git clone --depth=1 https://github.com/majiayu000/claude-skill-registry "$T" && mkdir -p ~/.claude/skills && cp -r "$T/skills/data/antibody-design" ~/.claude/skills/majiayu000-claude-skill-registry-antibody-design && rm -rf "$T"
manifest:
skills/data/antibody-design/SKILL.mdsource content
---name: antibody-design-agent description: An advanced agent for de novo antibody design and optimization using state-of-the-art protein language models (MAGE, RFdiffusion). license: MIT metadata: author: VUMC / UW Baker Lab version: "1.0.0" compatibility:
- system: Python 3.10+
- hardware: GPU required (A100/H100) allowed-tools:
- run_shell_command
keywords:
- antibody-design
- automation
- biomedical measurable_outcome: execute task with >95% success rate. ---"
Antibody Design Agent
This skill brings together cutting-edge tools for antibody engineering, including MAGE (Monoclonal Antibody Generator) and RFdiffusion for Antibodies. It enables the de novo design of antibodies against specific viral or tumoral targets.
When to Use This Skill
- De Novo Design: Generating antibody sequences/structures that bind to a specific antigen.
- Epitope Targeting: Designing VHH or binders for a specific epitope on a target protein.
- Optimization: Improving the affinity or stability of an existing antibody candidate.
- Viral Defense: Rapidly generating antibodies against novel viral strains.
Core Capabilities
- MAGE (Monoclonal Antibody Generator): Uses a protein language model to generate diverse antibody sequences against unseen viral strains.
- RFdiffusion for Antibodies: Generates 3D antibody structures that bind to a target structure with high precision.
- ProteinMPNN: Optimizes the sequence of the generated structures for solubility and expression.
Workflow
- Target Definition: Input the PDB structure or sequence of the antigen (target).
- Design Phase:
- Use RFdiffusion to generate the backbone of the binder (CDR loops).
- Use ProteinMPNN to design the sequence for the backbone.
- Alternatively, use MAGE to generate sequences directly from viral strain data.
- Validation (In Silico): Use AlphaFold3 or ESMFold to predict the complex structure and assess binding confidence (pLDDT, PAE).
- Selection: Rank candidates for synthesis.
Example Usage
User: "Design a VHH nanobody that binds to the RBD of the SARS-CoV-2 KP.2 variant."
Agent Action:
- Retrieves RBD structure for KP.2.
- Runs
with "binder" constraints on the RBD surface.RFdiffusion - Generates 100 backbone candidates.
- Sequences them with
.ProteinMPNN - Folds the complexes with
to verify binding interface.AlphaFold3 - Returns top 5 sequences.