If you are a drug discovery firm dealing with protein targets for diseases with high unmet need that are too unstable to study — this project developed a stabilization technology that delivers minimally modified proteins with retained functionality.
Universal Protein Stabilization Technology for Better Drugs and Diagnostics
Proteins are like delicate origami; if they unfold or lose their shape, they stop working. This technology acts like a molecular brace, keeping them stable and active even in harsh conditions where they would normally break down. It allows scientists to use powerful proteins that were previously too fragile for real-world use.
What needed solving
Many high-potential proteins for medicine and industry cannot be used because they are unstable and lose their activity outside of very specific physiological conditions.
What was built
A stabilization technology combining structural biology, molecular biology, and chemistry, including a computational design tool for predicting modification sites.
Who needs this
Who can put this to work
If you are a point-of-care device manufacturer dealing with proteins that lose activity outside of a lab setting — this project developed a universal solution to stabilize proteins for biomedical applications.
If you are a chemical production plant dealing with proteins that break down during industrial processes — this project developed a technology to maintain structural integrity under non-physiological conditions.
Quick answers
What is the estimated cost or pricing for this technology?
Based on available project data, specific pricing is not mentioned, but the technology aims to replace costly and time-consuming trial-and-error stabilization approaches.
Can this be scaled to industrial levels?
The project is currently validating the technology in a real operating environment at TRL5 to ensure it can be applied to a broad range of proteins for industrial and biomedical use.
What is the IP and licensing strategy?
Based on available project data, the coordinator intends to offer B2B services to customers and develop an internal drug discovery pipeline.
How does this integrate into existing workflows?
The project is establishing a time-efficient workflow that includes a computational tool for design and prediction of modification sites followed by a production process.
What is the timeline for market availability?
The project period runs from 2022-06-01 to 2025-05-31, focusing on reaching TRL5 validation.
Who built it
The consortium is lean, consisting of 2 partners from the Netherlands and Poland. It is led by Incircular B.V., an SME, with a 50% industry ratio, combining a commercial entity with a research partner to move the technology from lab validation to a real operating environment.
Contact Incircular B.V. in the Netherlands
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