Information propagation through enzyme-free catalytic templating of DNA dimerization with weak product inhibition

Information propagation by sequence-specific, template-catalyzed molecular assembly is a key motif facilitating life’s biochemical complexity, allowing the production of thousands of sequence-defined proteins from only 20 distinct building blocks. By contrast, exploitation of catalytic templating is rare in non-biological contexts, particularly in enzyme-free environments, where even the template-catalyzed formation of dimers is challenging. The main obstacle is product inhibition: the tendency of products to bind to templates more strongly than individual monomers, preventing catalytic turnover. We present a rationally designed enzyme-free system in which a DNA template catalyzes, with weak product inhibition, the production of sequence-specific DNA dimers. We demonstrate selective templating of 9 different dimers with high specificity and catalytic turnover; we then show that the products can participate in downstream reactions, and that the dimerization can be coupled to covalent bond formation. Most importantly, our mechanism demonstrates a rational design principle for engineeringinformation propagation by molecular templating.

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Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2024-12-26
DOI
https://doi.org/10.5281/zenodo.14959246
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
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article

Information propagation through enzyme-free catalytic templating of DNA dimerization with weak product inhibition

Zenodo (CERN European Organization for Nuclear Research)
Cyclopropane Reaction Mechanisms
article

Information propagation through enzyme-free catalytic templating of DNA dimerization with weak product inhibition

article en

Abstract

Information propagation by sequence-specific, template-catalyzed molecular assembly is a key motif facilitating life’s biochemical complexity, allowing the production of thousands of sequence-defined proteins from only 20 distinct building blocks. By contrast, exploitation of catalytic templating is rare in non-biological contexts, particularly in enzyme-free environments, where even the template-catalyzed formation of dimers is challenging. The main obstacle is product inhibition: the tendency of products to bind to templates more strongly than individual monomers, preventing catalytic turnover. We present a rationally designed enzyme-free system in which a DNA template catalyzes, with weak product inhibition, the production of sequence-specific DNA dimers. We demonstrate selective templating of 9 different dimers with high specificity and catalytic turnover; we then show that the products can participate in downstream reactions, and that the dimerization can be coupled to covalent bond formation. Most importantly, our mechanism demonstrates a rational design principle for engineeringinformation propagation by molecular templating.

Zenodo (CERN European Organization for Nuclear Research)
University of Surrey (GB), University College London (GB), Imperial College London (GB)
Openalex Percentile: Top 73%
Cyclopropane Reaction Mechanisms
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