A New Architecture for DNA‐Templated Synthesis in Which Abasic Sites Protect Reactants from Degradation

Jennifer Frommer, Robert Oppenheimer, Benjamin M. Allott, Samuel Núñez‐Pertíñez, Thomas R. Wilks, Liam R. Cox, Jonathan Bath, Rachel K. O'Reilly*, Andrew J. Turberfield*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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 languageEnglish
Article numbere202317482
JournalAngewandte Chemie
Early online date12 Feb 2024
DOIs
Publication statusE-pub ahead of print - 12 Feb 2024

Bibliographical note

Research Funding
Engineering 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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