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Unlock protein design's new frontiers with AI

Interlit is an AI protein design company.

We engineer high-affinity protein binders and rank the most clinically viable therapeutic candidates, providing transparency into the metrics driving each ranking.

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Dr. Shen Yan has joined Interlit as co-founder and Chief Scientific Officer, with a PhD in Molecular and Translational Biomedicine, an MBA, and 15+ years of wet lab experience. Read more

01

The next protein therapy is hiding in a vast space

A single antibody sequence has more possible variants than atoms in the observable universe.

A 100-residue protein domain has 20^100 (about 1.3x10^130) possible sequences; the observable universe holds an estimated 10^80 atoms.

02

Designing from scratch is a lottery

It is prohibitively expensive to test every candidate, and most fail late for reasons that have nothing to do with binding: developability, aggregation, immunogenicity.

03

Glass-box, not black-box

We open the ranking, so you see why each candidate scores as it does.

The EMA states an a priori preference for transparent, interpretable models. (EMA reflection paper on AI in the medicinal product lifecycle, 2024.)

Start from what works

We start from your starting sequence(s), design new therapeutic protein binders for the desired target, and rank the most clinically viable candidates, narrowing down to a few you can test.

See every risk metric

Each ranking shows its developability and immunogenicity scores, so you decide which risks matter most for your pipeline.

Lower costs, faster cycles

Fewer designs to synthesize means less wet-lab spend and a shorter research cycle.

The lab results

Proven in the lab

In the 2026 EGFR/cetuximab binder optimization competition, three of our ten designs surpassed the previous world best, and the candidate we ranked first proved to be the tightest binder measured, at 43.9 times tighter than the cetuximab starting antibody and 1.6 times tighter than the best prior design, all done in under one day.

Best measured affinity per approach against the 9.94 nM cetuximab parent (fold better; wet-lab Kd). The previous best public design (scarlet-seal-granite) held 0.37 nM. Three of our ten shortlisted candidates bound more tightly; the Interlit bars carry our in silico method's ranking (#1, #6, #9), and the one we ranked first was also the tightest binder measured. Independently measured by Adaptyv (SPR).
  • 43.9x tighter binding affinity than the approved cancer drug, cetuximab
  • 10 of 10 ranked candidates bound to their target in the lab
  • 3 of 10 designs surpassed the previous world record
  • under 1 day from zero to one, from start to finish, under limited compute

Affinities independently measured by Adaptyv, an independent wet-lab partner (SPR), as measured mid-July 2026. "World best" means the best publicly recorded result we are aware of in Adaptyv's competition data.

How the field reacted

10 out of 10 candidates actually binding is already a great achievement, but having 3 even higher affinity than the previous best is amazing!
Estelle Grosjean Scientist & Project Manager On our LinkedIn post
Interlit's founder

Our story

In under a day, we set three world records in protein design.

A two-person team I led set a world best in the 2026 EGFR/cetuximab binder optimization competition. The secret? While most teams ranked their candidates using AlphaFold confidence scores like ipTM or ipSAE, we focused on selecting the tools and metrics that correlate with the physical reality of protein binding. Today I'm building Interlit, an AI protein design company, to help biotech and pharmaceutical teams push protein design's frontier.

Frequently asked questions

We are an AI-native protein design company, helping drug-discovery teams turn a promising sequence into a lab-ready, defensible shortlist.
Our core focus is protein optimization. We prefer to start from a sequence, or a few, then we propose new candidate sequences and rank the best ones, to save you from testing every sequence. That reduces your experimental cost and accelerates your research lifecycle.
Interlit offers a clear rationale for why one sequence ranks above another, so you can decide for yourself whether a given metric, such as immunogenicity risk or developability and manufacturability, matters more than another.
We are focused on building the best AI protein design company, so at the moment we do not offer wet-lab services ourselves.
It depends on the pricing tier you pay for; please refer to our Terms and Conditions. Basically, at the standard tier you keep the IP. At the discount tier, we either co-own the IP or you allow us to train our models on the results.
Early access is open on request. Please fill out the form below and we will reach out to you as soon as we can.
No. Adaptyv is an independent company that predates us and provides lab services to us. That keeps our results unbiased, independently validated by wet-lab partners the industry already trusts.

Early access

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