Data — I Beat Claude on TNFα for $677

Both arms of both targets, the per-engine scores behind the selection, and the binding kinetics from Adaptyv Bio. Released under ODC-BY.

File What it is
tnfa_designs.csv All 20 TNFα sequences. Control = TRUE is the arm with the sequence/structure co-optimization stage removed.
pdl1_designs.csv All 20 PD-L1 sequences, same convention.
engine_scores.csv Per-design scores from every co-folding engine used for selection: Boltz-2, AlphaFold2, Protenix, RFdiffusion3, OpenFold3, ESMFold2. ipSAE, RMSD, pLDDT, pTM, ipTM, interface PAE. Also the consensus rank each design was selected on.
tnfa_binding_summary.csv Binding calls and fitted kinetics per design: per replicate and overall. binding, binding_strength, kd_app with CIs, kon, koff, fit quality, the fitted model, and the sequence.
pdl1_binding_summary.csv Same for PD-L1.
tnfa_kinetics/ The fit-level tables behind the summary: fits.csv, reads.csv, replicates.csv, blanks.csv, plus the binding models — equations, parameters and units.

What is not here

The raw response curves and sensorgram plots — one per concentration per replicate, 46 MB. Ask and I will send them.

Caveats that matter when you read these numbers

  • The TNFα run is not closed. 19 of the 20 designs have both replicates. TNFA_OPT_08 currently has one. Its overall row is that single replicate.
  • kd_app is apparent, not monovalent. TNFα is a homotrimer and the binder is the immobilized partner, so avidity is built into this format. Several fits sit at the koff floor of 1e-5 /s, which means the off-rate was too slow to resolve in the dissociation window, not that it was measured to be that value.
  • Antigen: ACROBiosystems TNA-H4211, the same catalogue number MIT used for BoltzGen. Anthropic used TNA-H5228.
  • Measured by Adaptyv Bio, BLI, five-point concentration series, duplicate.

Anthropic’s data for the same target is at Anthropic/claude-protein-binder-design under CC-BY-4.0. Every figure in the post can be rebuilt from those two sources.