
UK biotech startup Latent Labs has released Latent-X, an internet-based generative AI tool that enables scientists to design protein binders with no coding required. The advance may dramatically reduce barriers to drug discovery. The action is being touted as a push in the direction of ‘push-button biology’, in which intricate biomolecular engineering is made possible via an internet browser.
Founded by Simon Kohl, a former DeepMind scientist who worked on AlphaFold2, the company states that its platform allows users to upload a protein structure, select hotspots, and create binders such as macrocycles and mini-binders, all within hours.
Whereas AlphaFold changed the world of structural biology by predicting protein binding design and structure, Latent-X does more. It designs brand-new proteins from scratch.
That’s a difference that matters. Rather than merely predicting how a particular sequence would fold, Latent-X creates new protein sequences with customized binding properties, providing a revolutionary new avenue for targeted therapeutics.
Early lab results reported by the company indicate 91–100% success rates for macrocycles and 10–64% for mini-binders, with picomolar-level binding affinity in a few instances, an essential measure of pharmaceutical effectiveness.
Latent Labs raised $50 million from a prominent roster of investors, including Radical Ventures, Sofinnova, and technocrats such as Jeff Dean, Aidan Gomez, and Dario Amodei.
The group boasts alumni from DeepMind, Microsoft, Stability AI, Apple, and Zymergen, an indication of serious cross-disciplinary muscle.
Unlike most drug discovery companies powered by AI, which target internal pipelines, Latent Labs aims to license its platform, similar to a software-as-a-service (SaaS) model, to researchers, academics, and biotech companies worldwide.
Latent-X’s no-code aspect is more than simply an easy-to-use interface; it may be a game-changing leveler in the extraordinarily technical domain of bioengineering. Researchers who lack advanced machine learning knowledge or access to supercomputers can now produce structure-validated protein prospects on a laptop.
For a sector where early-stage screening is expensive and time-consuming, Latent-X may significantly shorten discovery cycles, making therapeutic innovation faster, cheaper, and more inclusive.
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As synthetic biology gets more programmable, Latent Labs’ strategy is notable not just for its accessibility but also for its scalability. If the platform meets its early potential, Latent-X might be the catalyst for a new generation of decentralized drug discovery, from Boston laboratories to Bengaluru.