Uncategorized
Biohub Releases Protein Biology World Model to Address Disease
Biohub Releases Protein Biology World Model to Address Disease
Biohub, the non-profit research organization co-founded by Priscilla Chan, MD, and Mark Zuckerberg, has now unveiled the latest update to the ESM protein language model family, with expanded capabilities in binder design and protein function mapping for therapeutic discovery. The release comes just seven months after Biohub recruited the team behind EvolutionaryScale.
The system includes ESMC (Evolutionary Scale Modeling Cambrian), a language model trained on approximately 2.8 billion sequences drawn from a breadth of life, including organisms adapted to extreme environments, and more than 20,000 types of proteins found in the human body. Evolutionary information encoded in ESMC is translated into atomic-resolution protein structures and interactions using the design engine and prediction model, ESMFold2.
Alex Rives, PhD, head of science at Biohub and former chief scientist at EvolutionaryScale, presented the work at this week’s “AI in Biology” symposium at Cold Spring Harbor Laboratory.
These models aim to transform the earliest stages of drug discovery by making biology more programmable. While traditional discovery workflows rely on slow and resource intensive experimental screens to identify promising drug candidates, rational protein design guided by in silico predictions has the potential to dramatically accelerate development timelines.
“We’re at an exciting point in protein biology where accurate digital representations allow asking experimental questions at a scale that wouldn’t be possible in the laboratory,” Rives told GEN Edge.
![ESMC provides a foundation for modeling the sequence, structure, and function of proteins. ESMFold2 predicts the structure of proteins and biomolecular complexes. Features derived from the representations of the model capture fundamental principles of structure and function that form a compositional grammar for protein biology. [Biohub]](https://www.genengnews.com/wp-content/uploads/2026/05/Viz1-11-1024x576.png)
ESMFold2 designed high-affinity protein binders against five disease targets in cancer and immunology: receptor tyrosine kinases implicated in tumor growth (EGFR and PDGFRβ), immune checkpoints exploited by cancer cells to evade immune surveillance (PD-L1 and CTLA-4), and a regulator of immune cell signaling (CD45).
Lab-validated designs achieved hit rates ranging from 36–88% for compact mini-binders and 15–29% for antibody-derived formats, while also demonstrating nanomolar binding affinity, high specificity, and favorable stability profiles consistent with potential clinical utility. Notably, binders for PD-L1 showed therapeutic function and restored T-cell signaling in laboratory tests by blocking the same pathway as approved checkpoint therapies.
Rather than requiring multiple sequence alignments (MSAs) to build representations, ESMFold2 captures evolutionary information encoded during pretraining. The model also uses a looped transformer architecture, which allows compute to scale at inference time and avoids overfitting that can arise when training is constrained by limited experimental protein structures.
In benchmarking, ESMFold2 performed favorably when compared against Chai-1 from Chai Discovery, Boltz-1 from MIT (whose developers have since launched a public benefit corporation), and AlphaFold 3 from Google DeepMind.
The models are accessible under the highly permissive Massachusetts Institute of Technology (MIT) license for both commercial and non-commercial use. The work is described as a preprint that has not yet been peer reviewed.
“All in” on AI biology
Last November, Chan and Zuckerberg made the pledge to go “all in on AI-powered biology,” announcing that the organization’s scientific teams will now unite under a single entity, known as Biohub, where the duo would place the majority of their philanthropic effort.
Concurrently, Rives and EvolutionaryScale colleagues were recruited to tackle disease by decoding the “grammar” of amino acids through billions of years of evolution. That same mission had once secured a whopping $142 million seed round when the startup unveiled in 2024. The raise was led by Nat Friedman, Daniel Gross and Lux Capital, and included participation from Amazon Web Services (AWS) and NVentures, Nvidia’s corporate venture arm.
Biohub continues to advance virtual biology by building digital representations of molecules, genomes, cells, and living systems. The new ESM release joins Biohub’s growing ecosystem of biology models, including TranscriptFormer, which was published in Science earlier this month.
The organization recently invested $500 million in the Virtual Biology Initiative, a five-year campaign to accelerate the creation of technologies and multi-modal datasets to build predictive models of biology. The commitment comes a few months after the organization announced a collaboration with Arc Institute and Tahoe Therapeutics to build the largest single cell chemical perturbation dataset to power the virtual cell.
Evolution is all you need
Biohub has applied the new ESM models to generate the ESM Atlas, a mapping of 6.8 billion sequences and 1.1 billion predicted structures to protein function using ESMC’s representations. Generating this atlas would have taken “billions of years of experimental work,” but was condensed into a couple of weeks with computational inference. The ESM Atlas is released open-source.
By probing ESMC’s representations using sparse autoencoders (SAEs), a technique for identifying interpretable structure in large language models, the authors found that the model independently learned hierarchical organization covering the basic chemistry of individual amino acids, local structural interactions, and functional concepts across unrelated proteins, despite being trained only on sequence data.
Notably, ESM Atlas SAE feature clusters brought together RNA-guided DNA endonucleases, eukaryotic Fanzor proteins and their evolutionary ancestor, prokaryotic TnpB, despite their high evolutionary divergence and low sequence similarity. These insights could support the development of new gene-editing tools.
While the preprint’s results are still a step away from clinical impact, Rives reiterates the power of open science in placing these tools in the hands of researchers working directly in translational research.
Biohub is partnering with a number of platform partners, including AWS Bio Discovery, Benchling, Phylo, Tamarind Bio, Modal, Tool Universe, and SandboxAQ, to make the models widely available.
The post Biohub Releases Protein Biology World Model to Address Disease appeared first on GEN – Genetic Engineering and Biotechnology News.
Uncategorized
New webinar: Tackling drug discovery challenges in cancer research

Hosted by Drug Discovery World and supported by Sartorius and BioIVT, this webinar will explore the opportunities and challenges that exist within cancer research drug discovery and development.
You will hear from Dr Sudha Rao, Chief Scientific Officer of Kazia Therapeutics, Karol Budzik, PhD, Business Development Associate at Vyriad Therapeutics and Lars van der Veen, Chief Scientific Officer at iOnctura.
Presentations will cover how cancer treatments have shifted towards reprogramming the biology driving tumour growth, immune escape and treatment resistance, the trajectory that in vivo CAR-T treatments are taking, and how challenging tumours burdened by stroma and immune-mediated resistance can be tackled.
Q&A with the speakers follows the presentations.
The post New webinar: Tackling drug discovery challenges in cancer research appeared first on Drug Discovery World (DDW).
Uncategorized
Psilocybin proves promising in neuropathic pain mouse study
Amid the rise of psychedelics in the mental health space, researchers have begun to explore psilocybin as a treatment for chemotherapy-induced peripheral neuropathy.
Uncategorized
New Spectrometry Technique Could Aid Formulation Development
New Spectrometry Technique Could Aid Formulation Development
A new technique combining two forms of spectrometry could help biopharmaceutical companies improve their choice of formulation buffer for antibody manufacturing by revealing how molecular forms and three-dimensional shapes of complex biologics respond to their environment. That’s the view of Christian Bleiholder, PhD, a professor at Florida State University who helped develop the technique.
According to Bleiholder, what happens structurally when a complex biological molecule, such as an antibody or viral spike protein, binds to its target is currently poorly understood.
“This is where [this approach] can help with the bioprocessing and formulation,” he says, as structural changes “can affect the lifespan [of the product] and lead to issues, such as aggregation.”
Because antibodies are complex, existing techniques tend to be powerful at different levels of complexity, he explains. Mass spectrometry is particularly powerful for distinguishing molecular composition, while structural approaches such as X-ray crystallography and cryo-electron microscopy can provide high-resolution structural information.
The challenge is understanding the link between these things within a heterogeneous sample, he says.
To overcome this, Bleiholder and his team worked with Bruker Daltonics to develop Tandem-Trapped Ion Mobility Spectrometry (Tandem-TIMS). This combines tandem ion mobility spectrometry with tandem mass spectrometry to disentangle three overlapping layers of molecular complexity: molecular form, three-dimensional shape, and binding or assembly state, he says.
He explains that, if the proteins have different structures, they can be characterized with tandem ion mobility spectrometry, and then mass spectrometry can be used to look at their molecular forms and binding states.
Going forward, Bleiholder hopes the technique can be used for formulation development but also earlier, during drug discovery of new products, such as multi-specific antibodies, to determine which molecular states are important and how those change when a biologic engages its target. He also plans to look at automating the technique.
Bleiholder spoke about using Tandem-TIMS at the Bioprocessing Summit in Boston earlier this year.
The post New Spectrometry Technique Could Aid Formulation Development appeared first on GEN – Genetic Engineering and Biotechnology News.
-
Uncategorized8 months agoNovartis buys Synnovation’s PI3Kα inhibitors for $3 billion
-
Endpoints News8 months ago
Novartis to pay $2B upfront to take next-gen PI3Kα inhibitor from Synnovation
-
Uncategorized6 months agoOptical Pooled CRISPR Screen Reveals Regulators of NF-κB Dynamics in Human Cells
-
Uncategorized6 months ago
Relay’s PI3Kα inhibitor clears efficacy bar in Phase 2 vascular anomalies study
-
Uncategorized5 months ago
Hybrid solid−liquid optics enable scalable, high-resolution light-sheet microscopy across diverse immersion media
-
Fierce Biotech7 months ago
Scientists turn pig semen extract into eye drops that kill cancer in mice
-
Nature Biotechnology8 months ago
Sustained nitric oxide production by engineered E. coli remodels the tumor microenvironment and potentiates immunotherapy
-
Nature Biotechnology7 months ago
Mapping cis-regulatory mutations at scale in sorghum enables modulation of gene expression
Scan to Read