Ranomics
Antibody structure rendered with highlighted CDR loops for developability analysis
Free research tool

Binder Developability Scout

Score any antibody, nanobody, or designed binder across five developability dimensions (humanness, liability motifs, charge, hydrophobicity, aggregation) before committing designs to synthesis.

Free to use. No credit card required. Sign up and start scoring.

Built for antibody engineers triaging panels, de novo designers filtering RFdiffusion and BindCraft outputs, and groups preparing humanized Mabs for clinical candidacy.

How it works

From sequence to developability report in minutes

01

Paste a sequence

Input a VH/VL pair, scFv, VHH, or de novo binder as FASTA or plain text. Multiple sequences scored in a single batch.

02

Five-dimension scoring

Humanness, liability motifs, charge and pI, hydrophobic patches, and aggregation propensity combined into a 0-1 composite.

03

Annotated results

Per-residue heatmap of liability hotspots, CDR-level breakdown, and side-by-side comparison across a panel.

04

Export for your team

Download a CSV of scores and annotated residues, or a PDF report ready to drop into a design review.

Scoring methodology

Five-dimension composite developability score

Each binder is scored on a 0-1 scale combining five dimensions drawn from published antibody developability literature and industry CMC practice. Higher scores indicate molecules more likely to survive downstream manufacturing, formulation, and clinical development.

20%

Humanness

Germline similarity against the IMGT reference and repertoire frequency against OAS. Lower deviations from observed human antibodies reduce immunogenicity risk and simplify humanization.

20%

Liability motifs

Sequence-level scan for deamidation (NG, NS), isomerization (DG, DS), N-linked glycosylation (NXS/T), methionine oxidation, and unpaired free cysteines. Each motif flagged with position and CDR context.

20%

Charge and pI

Theoretical isoelectric point, net charge at physiological pH, and VH/VL charge asymmetry. Extreme pI or mismatched VH/VL charges predict poor solubility and heightened viscosity at formulation concentrations.

20%

Hydrophobic patches

Kyte-Doolittle sliding-window hydrophobicity with CDR-specific weighting. Surface-exposed hydrophobic patches drive non-specific binding, poor HIC retention, and elevated aggregation risk.

20%

Aggregation propensity

Per-residue aggregation propensity from published hydrophobicity-weighted scales, with aggregation-prone region (APR) detection. Flags contiguous hydrophobic and beta-sheet-prone stretches associated with self-association.

When to use Developability Scout

Catch liabilities before they become attrition

Most developability failures are visible in the sequence long before a molecule reaches a stability study. A deamidation hotspot in CDR-H2, a glycosylation site at a CDR tip, or extreme pI mismatch between chains: all correctable if caught early, costly if caught at scale.

Developability Scout surfaces these liabilities in a consistent, literature-backed report so every candidate in your campaign is triaged the same way. Use it between design and synthesis, between screening and lead nomination, or on any binder you are considering putting into a wet-lab pipeline.

After running RFdiffusion or BindCraft, before committing de novo designs to gene synthesis

Triaging an in-house antibody panel for CMC-blocking liabilities before expression

Evaluating a humanized Mab before freezing the sequence for clinical candidacy

Checking naive yeast display hits for developability before progressing to affinity maturation

Comparing VH/VL pairings and CDR variants from campaign outputs on a single scorecard

Start scoring your binders

Developability Scout is free. Sign up, paste a sequence, and get a scored report in seconds. Or talk to us directly about binder design and developability engineering.