Human health
- Disease biomarkers
- Cancer
- Infectious disease
- Autoimmune disease
- Cardiovascular disease
- Neurological disease
AI · Structural biology · Protein engineering
We design novel binding proteins for targets across healthcare, diagnostics, agriculture, food, industrial biotechnology and environmental monitoring. From biological target to functional binder — designed computationally, built experimentally.
Approach
Biology runs on molecular recognition. Antibodies became the default tool for detecting, capturing and modulating biological molecules — but discovery is slow, expensive, and bounded by what nature happened to evolve.
Altered Protein is building an AI-native approach to designing binders for targets that are difficult, expensive or impractical to address conventionally.
Instead of searching nature for the right binder, design the binder you need.
The design loop
Generative design, sequence engineering, structure prediction and experimental validation, joined into one continuous discovery loop.
Start from a biological target — a structure, a sequence, an epitope.
Generate candidate binding proteins computationally with generative and protein foundation models.
Evaluate structure, binding geometry, stability and developability before anything enters the lab.
Express and experimentally test the most promising candidates.
Return every measurement — including the failures — to the design process.
Improve affinity, specificity, stability and manufacturability. Then run it again.
Back to 01. Every validated design becomes information. So does every failure.
The objective is not to predict proteins. It is to design proteins that work.
Design space
Engineered proteins can be designed around what an application actually requires, rather than around what a screen happens to return.
This moves protein engineering from discovery by screening toward design followed by validation.
The engine
A computational stack that connects protein generation, sequence design, structural prediction and functional evaluation.
Novel protein backbones and binding architectures.
Amino-acid sequences optimised for the intended structure and function.
Candidate structures and target–binder interfaces, modelled before synthesis.
The properties that decide whether a designed protein can become a product.
Laboratory measurement as ground truth for the next generation of designs.
A compounding engine: each cycle starts better informed than the last.
From digital design to physical biology
The bottleneck in protein engineering is not generating another sequence. It is closing the loop between computation and reality — so that every experiment makes the next design decision more informed.
Platform
Protein binders are a horizontal technology. The same underlying design capability produces molecular recognition systems for very different problems.
Different markets. The same fundamental capability: design a protein that recognises what you need.
Why now
ComputeDesignBuildTestLearn
And the loop is getting faster.
Partnerships
We work with organisations that have challenging biological targets and need new molecular recognition: poorly characterised targets, low-abundance biomarkers, highly specific molecular signatures, difficult protein surfaces, and applications with unusual stability or manufacturing requirements.
Partner with us lab@alteredprotein.com
Let's engineer biology differently.