The automated lab for agentic biology

We have been selected by @ARIA_research as an Activation Partner and are expanding to London. As part of the programme, we’re opening a lab in London and will work with ARIA-funded teams to build the experimental capabilities their protein design programmes need. Those new assays and modalities will plug into Adaptyv’s existing lab and data infrastructure, giving them the same scale, speed and ease of access as the rest of the platform. This new experimental infrastructure will be built and operated in the UK, expanding what ARIA-funded teams and the wider UK protein design ecosystem can build and test. We think the UK is one of the best places in the world to build at the intersection of AI and biology, with exceptional teams across protein design, biotech and AI already here. We’re excited to become a deeper part of that ecosystem and help enable the next wave of companies building here.
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Adaptyv Bio retweeted
Bindcraft2 🤝 Claude 🤝 Adaptyv apply for our protein design competition and solve all the challenges docs.google.com/forms/d/e/1F…
ʙɪɴᴅᴄʀᴀꜰᴛ2 is out, and we're not waiting for the paper. The full code drops today, free for academic and industry use. We're releasing it early so you can start designing right now, and bring its full power to the current Adaptyv competition. github.com/PacesaLab/BindCra…
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Back in 2024, BindCraft1 emerged as one of the strongest methods in our protein design benchmarks, winning our first EGFR competition and becoming one of the most widely used approaches in the following round. We’re happy to see BindCraft2 released just in time for our new protein design competition with Anthropic, where more than 5,000 designs will be experimentally tested in our lab. Show us what you can do with BindCraft2!
ʙɪɴᴅᴄʀᴀꜰᴛ2 is out, and we're not waiting for the paper. The full code drops today, free for academic and industry use. We're releasing it early so you can start designing right now, and bring its full power to the current Adaptyv competition. github.com/PacesaLab/BindCra…
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We’re partnering with @Anthropic to launch the biggest Protein Design Competition in the world, challenging people around the world to use AI to design new potential drug candidates for diseases that affect millions of lives. The competition will feature five challenges, each focused on a specific disease or biological mechanism. Compared to previous competitions, it will be a big step-up in complexity and scale to push the boundaries of AI-driven protein design. Together with Anthropic, we’re sponsoring over $1 million in experimental validation, making it possible to test more than 5,000 protein designs in our automated lab at no cost to participants. Anthropic is providing an additional $1 million in Claude credits. All experimental results will be published openly on @Proteinbase, including designs that didn’t work, so anyone can access the data and build on what we learn. The competition is open to everyone and free to enter. It will feature 3 tracks: - Track 1 is aimed at expert protein designers, with up to 20 teams to be selected. - Track 2 is targeting life science academics and industry researchers. - Track 3 is open to everyone from tech enthusiasts to high-school students. By combining Anthropic’s models with access to our automated lab, we want to make it possible for anyone with a laptop and an internet connection to join the global effort to advance human health with AI. A big thanks to @Modal for contributing compute for protein design and to @TwistBioscience for contributing the DNA for the experimental validation! Sign up link below -
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We're bringing experimental validation to @OpenAI's Rosalind Workbench through the Adaptyv API. Rosalind Workbench is a new way to orchestrate complex life science research workflows across models and specialized scientific tools. Through the Adaptyv API, those workflows can now run full design–build–test–learn cycles in our wet lab, with real experimental data feeding directly into the next round of designs.
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We raised a $40M Series A to build the automated lab for agentic biology. Last week, we shared the work we did with @Anthropic: Claude designed proteins, sent them to our automated wet lab, and got real experimental data back. We believe this is where biology is going: AI agents designing experiments, running them in automated wet labs, learning from the results and iterating. But AI can only move as fast as the experiments behind it. To use the potential of AI to cure all diseases, we need to build high-throughput wet lab infrastructure: a “biological gigafactory”. That’s exactly what we’re doing at Adaptyv. Over the past year we’ve grown our lab throughput by over 5x and onboarded more than 100 customers, ranging from bio AI labs like @chaidiscovery and @boltz_bio to pharmas like @Roche and @novonordisk to dozens and dozens of new startups that use AI to radically speed up drug discovery.
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The round was led by @HighlandEurope with existing investors ACE Ventures, @byFounders and @ycombinator doubling down.
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Now we’re scaling: doubling our team in Lausanne and opening a new office and lab in London in Q4 2026. If you want to work on hard problems across software, biology, and lab automation, join us: adaptyvbio.com/careers
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Adaptyv Bio retweeted
Using NVIDIA Proteina-Complexa, @muni_bio's autoresearch agent explored nearly 14,000 protein designs. @adaptyvbio validated nine TREM2 binders, three with sub-nanomolar affinity. The results show how agents can connect computational design with wet-lab feedback to improve the next round of discovery. 📘muni.bio/research/closing-th…
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AI has solved software. Biology is the next frontier. We're hiring across every team at Adaptyv. We’ve built the best automated lab for protein designers to experimentally test their AI-designed proteins. Today, the most advanced protein design companies run their wet-lab work on Adaptyv, from the biggest biopharmas to frontier AI labs to dozens of virtual biotech startups. Demand has grown faster than we have, so we’re hiring across the board: • Bio: Research associates, scientists and lab technicians to develop and run new assays at scale. • Lab automation: Engineers and interns to onboard new lab instruments and scale our automation infrastructure. • Software: Product and backend engineers to scale LabOS, our internal lab orchestration platform, our API for agents and the data pipelines that turn messy physical-world data into clean results. • Partnerships, customer success and operations: Building partnerships with AI & pharma labs, making sure customers understand their data and can run more campaigns, making sure the company operations run smoothly
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Step 4: you know where 👀
How to design your own PD-1 binder in 4 easy steps: 1. Download the tutorial notebook from the ESM team 2. Get a @modal API key to scale it up 3. Scaling it up, O($1000) will get you a 96 well plate of minibinders with >50% success rates on typical targets 4. Test it in the lab!
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Adaptyv Bio retweeted
We have fully open sourced our binder design protocol, which generates nanomolar affinity scFvs. The code here implements a faithful reproduction of the pipeline described in the paper, which is exactly what was used to produce our designs. Check it out here: tinyurl.com/7jnsuzv5
Replying to @THayes427
We’re excited to share the full binder design protocol. Check it out here: github.com/Biohub/esm/blob/m…. The notebook includes support for @modal to easily scale up binder generation. Give it a try and let us know how it works! You can read more about ESMFold2, ESMC, ESM Atlas, and the full results in the paper here: biohub.ai/papers/esm_protein….
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Adaptyv Bio retweeted
Binder design has come of age thanks to generative models—but how can we access the wider array of dynamic, multistate protein functions, so elegantly employed by nature? @mihirbafna14 and I are excited to share SwitchCraft, a framework for designing such functions. (1/7)
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What happens when you let frontier LLMs design proteins, and then synthesize and test them in a wet lab? We ran a protein design competition with @muni_bio where AI agents competed against humans to design molecules that bind TREM2, a key receptor linked to Alzheimer’s. Results: GPT 5.2 and Grok 4.1 both placed in the top 5, with molecules showing strong binding to TREM2 when tested in our lab.
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Honest caveat: we measured binding, on one target, in one day, which is the easy half of a therapeutic. We'd go as far as to claim binding is roughly solved. Whether agent-grade design holds for developability, immunogenicity, PK/PD or in vivo potency, we don't know yet.
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