De Novo Scaffold Design with Foldexa Scaffold

De novo protein design — creating proteins with no evolutionary precedent — is one of the most ambitious challenges in structural biology. With Foldexa Pipeline 2, it is now accessible to any researcher with a browser.

What Is De Novo Protein Design?

Classical protein engineering modifies naturally occurring proteins. De novo design starts from a blank slate: you define what a protein should do — bind a specific epitope, form a stable trimer, thread a catalytic motif — and the algorithm generates a backbone and sequence that achieves it. This unlocks protein functions that evolution never explored.

Foldexa Scaffold: Backbone Generation

Foldexa Scaffold, developed by the Baker Lab at the University of Washington, is a denoising diffusion probabilistic model fine-tuned from Foldexa Scaffold. It operates on protein backbone coordinates (N, Cα, C, O atoms), learning the joint distribution of residue positions in protein structures. Given a noisy backbone, it iteratively denoises toward physically realistic protein geometries.

Critically, Foldexa Scaffold supports partial diffusion — you can fix a target motif (e.g., the epitope contact residues from a viral antigen) and diffuse only the surrounding scaffold. This is the key capability we use in Pipeline 2.

Foldexa Pipeline 2 Workflow

1. 1Define the target motif: upload target PDB and specify residues to scaffold (e.g., chain A residues 45–67)
2. 2Configure scaffold parameters: total length (60–200 residues), secondary structure bias, symmetry (monomer, dimer, trimer)
3. 3Foldexa Scaffold generates N backbone structures (default N=100) conditioned on the fixed motif
4. 4Foldexa Sequence designs amino acid sequences for each backbone (3 sequences per backbone)
5. 5Foldexa Structure predicts the structure of each sequence and compares it to the Foldexa Scaffold backbone
6. 6Self-consistency filter: keep designs where Foldexa Structure RMSD < 1.5 Å to the Foldexa Scaffold backbone
7. 7Final ranking by Foldexa Score; top candidates returned with full structure files

The Self-Consistency Test

The self-consistency test is the most important filter in Pipeline 2. It asks: if we take the Foldexa Sequence sequence and predict its structure with Foldexa Structure, does it fold back into the Foldexa Scaffold backbone?

import foldexa

client = foldexa.Client(api_key="your_key")

# Submit de novo scaffold job
job = client.jobs.create(
    pipeline="foldexa-scaffold-design",
    motif_pdb="6VXX",
    motif_residues="A45-A67",
    scaffold_length=120,
    num_designs=100,
    sequences_per_design=3,
)

# Wait for completion
result = client.jobs.wait(job.id)

# Filter by self-consistency RMSD
top = [
    d for d in result.designs
    if d.self_consistency_rmsd < 1.5
    and d.foldexa_score >= 0.80
]
print(f"{len(top)} designs passed all filters")

Benchmark: Viral Epitope Scaffolding

We benchmarked Pipeline 2 on three viral epitope scaffolding tasks: RSV site II (F protein), SARS-CoV-2 RBD ACE2-binding interface, and Influenza HA stem. For each, we generated 100 designs and measured self-consistency and scaffold quality.