adaptyvbio/protein-design-skills/solublempnn

Claude Code and agent skill by adaptyvbio/protein-design-skills

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Solubility-optimized protein sequence design using SolubleMPNN. Use this skill when: (1) Designing for E. coli expression, (2) Optimizing solubility of designed proteins, (3) Reducing aggregation propensity, (4) Need high-yield expression, (5) Avoiding inclusion body formation. For standard design, use proteinmpnn. For ligand-aware design, use ligandmpnn.

Install

npx vskill@latest install adaptyvbio/protein-design-skills/solublempnn

SKILL.md

SolubleMPNN Solubility-Optimized Design

Prerequisites

RequirementMinimumRecommended
Python3.8+3.10
CUDA11.0+11.7+
GPU VRAM8GB16GB (T4)
RAM8GB16GB

How to run

First time? See Getting started to set up Modal and biomodals.
Option 1: Modal (recommended)

SolubleMPNN is the soluble model type within the LigandMPNN wrapper:

bash
cd biomodals
modal run modal_ligandmpnn.py \
--input-pdb backbone.pdb \
--params-str "--model_type soluble_mpnn --number_of_batches 16 --temperature 0.1"

GPU: A10G default | Timeout: 900s default

Option 2: Local installation
bash
git clone https://github.com/dauparas/ProteinMPNN.git
cd ProteinMPNN
# The soluble weights are selected with --use_soluble_model, not a model name
python protein_mpnn_run.py \
--pdb_path backbone.pdb \
--out_folder output/ \
--num_seq_per_target 16 \
--sampling_temp "0.1" \
--use_soluble_model

Key parameters

ParameterDefaultDescription
--pdb_pathrequiredInput structure
--use_soluble_modeloffUse the solubility-trained weights
--num_seq_per_target1Sequences per structure
--sampling_temp"0.1"Temperature (string)
--model_namev_48_020Noise level (0.20 A); orthogonal to solubility

Model weights

--model_name sets the training-noise level (v_48_002 = 0.02 A, v_48_010 = 0.10 A, v_48_020 = 0.20 A), not a solubility tier. Solubility is a separate weight set chosen with --use_soluble_model, available for v_48_010 and v_48_020. Higher noise gives more sequence diversity.

Output format

output/
├── seqs/backbone.fa
└── backbone_pdb/backbone_0001.pdb

Sample output

Successful run
$ python protein_mpnn_run.py --pdb_path backbone.pdb --use_soluble_model --num_seq_per_target 8
Loading soluble model weights (v_48_020)...
Designing sequences for backbone.pdb
Generated 8 sequences in 2.1 seconds
output/seqs/backbone.fa:
>backbone_0001, score=1.31, global_score=1.24, seq_recovery=0.78
MKTAYIAKQRQISFVKSHFSRQLE...
>backbone_0002, score=1.28, global_score=1.21, seq_recovery=0.81
MKTAYIAKQRQISFVKSQFSRQLD...

What good output looks like:

  • Score: 1.0-2.0 (lower = more confident)
  • Reduced hydrophobic patches compared to standard MPNN
  • Improved charge distribution

Decision tree

Should I use SolubleMPNN?
│
├─ What expression system?
│ ├─ E. coli → SolubleMPNN ✓
│ ├─ Mammalian → ProteinMPNN (PTMs matter more)
│ └─ Yeast → Either
│
├─ History of expression problems?
│ ├─ Yes, aggregation → SolubleMPNN ✓
│ ├─ Yes, low yield → SolubleMPNN ✓
│ └─ No → ProteinMPNN is fine
│
├─ What's in the binding site?
│ ├─ Small molecule / ligand → Use LigandMPNN
│ └─ Nothing / protein only → SolubleMPNN ✓
│
└─ Optimizing for expression?
└─ Add --use_soluble_model to ProteinMPNN

Typical performance

Campaign SizeTime (T4)Cost (Modal)Notes
100 backbones × 8 seq15-20 min~$2Standard
500 backbones × 8 seq1-1.5h~$8Large campaign

Expected improvement: +15-30% solubility score vs standard ProteinMPNN.


Verify

bash
grep -c "^>" output/seqs/*.fa # Should match backbone_count × num_seq_per_target

Troubleshooting

Still insoluble: Confirm --use_soluble_model is set; redesign more positions or add explicit hydrophobic-residue bias Low diversity: Increase temperature to 0.2 Poor folding: Use standard ProteinMPNN and optimize later

Error interpretation
ErrorCauseFix
RuntimeError: CUDA out of memoryLong protein or large batchReduce batch_size
FileNotFoundError: v_48_020Missing model weightsDownload soluble weights

Next: Structure prediction for validation → protein-qc for filtering.

Security

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Source

Popularity

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Refreshed 17 Mar 2026, 7 months ago.

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