Abstract
The synthesis of artificial sequence‐defined polymers that match and extend the functionality of proteins is an important goal in materials science. One way of achieving this is to program a sequence of chemical reactions between precursor building blocks by means of attached oligonucleotide adapters. However, hydrolysis of the reactive building blocks has so far limited the length and yield of product that can be obtained using DNA‐templated reactions. Here, we report an architecture for DNA‐templated synthesis in which reactants are tethered at internal abasic sites on opposite strands of a DNA duplex. We show that an abasic site within a DNA duplex can protect a nearby thioester from degradation, significantly increasing the yield of a DNA‐templated reaction. This protective effect has the potential to overcome the challenges associated with programmable, sequence‐controlled synthesis of long non‐natural polymers by extending the lifetime of the reactive building blocks.
| Original language | English |
|---|---|
| Article number | e202317482 |
| Journal | Angewandte Chemie |
| Early online date | 12 Feb 2024 |
| DOIs | |
| Publication status | E-pub ahead of print - 12 Feb 2024 |
Bibliographical note
Research FundingEngineering and Physical Sciences Research Council. Grant Numbers: EP/L016494/1, EP/T000562/1, EP/T000481/1
Keywords
- DNA-templated synthesis
- DNA
- hydrolysis
- colocalization
- abasic
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A New Architecture for DNA‐Templated Synthesis in Which Abasic Sites Protect Reactants from Degradation
Frommer, J., Oppenheimer, R., Allott, B. M., Núñez‐Pertíñez, S., Wilks, T. R., Cox, L. R., Bath, J., O'Reilly, R. K. & Turberfield, A. J., 12 Feb 2024, (E-pub ahead of print) In: Angewandte Chemie (International Edition) . e202317482.Research output: Contribution to journal › Article › peer-review
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