Targeting the infectious potential of prions with DNA nanotechnology
Lead Research Organisation:
University of Kent
Department Name: Sch of Physical Sciences
Abstract
Amyloids are aggregates of misfolded proteins which are linked to neurodegenerative diseases, and can in some cases be infectious. The mechanistic links between amyloid structure and disease presentation are not yet understood, which means that there is an urgent need for new treatments. Understanding the relationship between their structure and biological role is challenging because it is difficult to isolate populations with single, static structures.
We present a new strategy which will enable study of the relationship between amyloid structure/polymerization state and infectivity, by putting DNA nanotechnology to work in controlling amyloid assembly. Using covalent and supramolecular interface of DNA with Sup35NM, an infective yeast amyloid-forming protein, the impact of programmed DNA hybridization upon the amyloid structure, polymorphism, and mechanical properties will be studied, enabling production of stable amyloid assemblies across a range of sizes.
The infective potential of the DNA-amyloid materials will then be studied by the expression of [PSI+] phenotype in yeast system which will give us unique and valuable new insights into the structural factors which influence amyloid infectivity, and thus assist in the understanding of neurodegenerative diseases and in production of new therapeutics.
We present a new strategy which will enable study of the relationship between amyloid structure/polymerization state and infectivity, by putting DNA nanotechnology to work in controlling amyloid assembly. Using covalent and supramolecular interface of DNA with Sup35NM, an infective yeast amyloid-forming protein, the impact of programmed DNA hybridization upon the amyloid structure, polymorphism, and mechanical properties will be studied, enabling production of stable amyloid assemblies across a range of sizes.
The infective potential of the DNA-amyloid materials will then be studied by the expression of [PSI+] phenotype in yeast system which will give us unique and valuable new insights into the structural factors which influence amyloid infectivity, and thus assist in the understanding of neurodegenerative diseases and in production of new therapeutics.
Organisations
Publications

Taylor ER
(2022)
Tuning dynamic DNA- and peptide-driven self-assembly in DNA-peptide conjugates.
in Chemical science
Related Projects
Project Reference | Relationship | Related To | Start | End | Award Value |
---|---|---|---|---|---|
EP/X01729X/1 | 01/12/2022 | 01/07/2023 | £201,710 | ||
EP/X01729X/2 | Transfer | EP/X01729X/1 | 02/07/2023 | 30/11/2024 | £138,533 |
Description | Our hypothesis that the formation of amyloid fibrils from individual proteins can be influenced by DNA hybridisation is so far supported by the results. We have evidence that specific base-pairing interactions between DNA and a modified protein can result in control of amyloid formation rate, and resulting size distributions. |
Exploitation Route | It is hoped that our results will lead to tools which could be used in the study of amyloid-related diseases such as Alzheimer's, and eventually lead to new therapies. |
Sectors | Healthcare Pharmaceuticals and Medical Biotechnology |