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鶹ýվ scientists unveil “Alenomers,” a new molecular platform that could rival antibodies

Published: 7 May 2026

Montreal, May 6, 2026– Researchers from 鶹ýվ have introduced a groundbreaking new class of molecules that could significantly reshape drug discovery and development. The technology, called Aptamer‑Like ENcoded OligoMERs (Alenomers), combines the advantages of antibodies and DNA‑based therapeutics while overcoming key limitations of both.

Antibodies are among today’s most successful medicines, but they are large, costly to manufacture, and can trigger immune side effects. Aptamers - short strands of DNA that can bind to disease targets - offer a promising alternative because they are smaller, easier to make and less immunogenic. However, from a chemical point of view, their simplicity has limited their real‑world therapeutic impact.

Alenomers overcome this challenge by introducing a wide range of synthetic chemical building blocks into aptamer‑like structures, while keeping a DNA “barcode” that allows researchers to rapidly identify the best performers through sequencing. Using this approach, scientists can test hundreds of thousands of chemically diverse molecules in parallel, dramatically accelerating discovery.

“Aptamers have fallen behind antibodies mainly because their chemistry is very limited, which makes them less stable in the body and harder to turn into effective medicines,”Hanadi Sleiman, Professor in the Department of Chemistry at 鶹ýվ.“Our approach removes this limitation by separating identification from function: enzymes only read a simple DNA barcode, while the attached aptamer can be built from much richer and more diverse chemistry. This allows aptamers to behave far more like antibodies,”concludes Prof Sleiman“with stronger binding, improved stability, and better performance in biological systems, opening new possibilities for how they can be used in medicine.”

Unlike earlier strategies that focused on improving just one property, alenomers are designed to enhance multiple features at once, including binding strength, stability, and overall function. The platform is also highly modular, allowing different aptamers, chemistries, and molecular architectures to be mixed and matched for specific applications.

“This is an elegant way to bring truly diverse chemistry into aptamers, far beyond what enzymes normally allow,”Maureen McKeague, Associate Professor in the Department of Chemistry at 鶹ýվ.“Instead of optimizing one molecule at a time, we can explore hundreds of thousands of variants in parallel, making the process faster, more efficient, and much less wasteful. What’s exciting is that this is not a oneoff solution. The platform is highly modular,” concludes Prof McKeague“and it feels like we’re only seeing the tip of what this chemistry can do for aptamer properties and realworld applications.”

Together, these advances position alenomers as a versatile discovery and development platform with clear pathstoward therapeutic translation. By combining antibody‑like performance with fully synthetic, scalable manufacturing, alenomers could lower development risk and enable new classes of precision molecular technologies for therapeutic and diagnostic applications across a broad range of clinical targets.

Read the full paper on Nature Chemistry

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