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

Author:

Frommer Jennifer1ORCID,Oppenheimer Robert2ORCID,Allott Benjamin M.34,Núñez‐Pertíñez Samuel34ORCID,Wilks Thomas R.34ORCID,Cox Liam R.34ORCID,Bath Jonathan34ORCID,O'Reilly Rachel K.1ORCID,Turberfield Andrew J.34ORCID

Affiliation:

1. School of Chemistry University of Birmingham, Edgbaston Birmingham B15 2TT United Kingdom

2. Department of Physics University of Oxford Clarendon Laboratory Parks Road Oxford OX1 3PU UK

3. Department of Physics University of Oxford Clarendon Laboratory Parks Road Oxford OX1 3PU UK

4. Kavli Institute for Nanoscience Discovery University of Oxford, Dorothy Crowfoot Hodgkin Building, South Parks Road Oxford OX1 3QU UK

Abstract

AbstractThe 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.

Funder

Engineering and Physical Sciences Research Council

Publisher

Wiley

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