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Template-dependent DNA Ligation for the Synthesis of Modified Oligonucleotides

Overview
Journal Nat Commun
Specialty Biology
Date 2024 Sep 13
PMID 39271668
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Abstract

Chemical modification of DNA is a common strategy to improve the properties of oligonucleotides, particularly for therapeutics and nanotechnology. Existing synthetic methods essentially rely on phosphoramidite chemistry or the polymerization of nucleoside triphosphates but are limited in terms of size, scalability, and sustainability. Herein, we report a robust alternative method for the de novo synthesis of modified oligonucleotides using template-dependent DNA ligation of shortmer fragments. Our approach is based on the fast and scaled accessibility of chemically modified shortmer monophosphates as substrates for the T3 DNA ligase. This method has shown high tolerance to chemical modifications, flexibility, and overall efficiency, thereby granting access to a broad range of modified oligonucleotides of different lengths (20 → 120 nucleotides). We have applied this method to the synthesis of clinically relevant antisense drugs and ultramers containing diverse modifications. Furthermore, the designed chemoenzymatic approach has great potential for diverse applications in therapeutics and biotechnology.

References
1.
Kosuri S, Church G . Large-scale de novo DNA synthesis: technologies and applications. Nat Methods. 2014; 11(5):499-507. PMC: 7098426. DOI: 10.1038/nmeth.2918. View

2.
Oda Y, Chiba J, Kurosaki F, Yamade Y, Inouye M . Additive-Free Enzymatic Phosphorylation and Ligation of Artificial Oligonucleotides with C-Nucleosides at the Reaction Points. Chembiochem. 2019; 20(15):1945-1952. DOI: 10.1002/cbic.201900217. View

3.
Moody E, Obexer R, Nickl F, Spiess R, Lovelock S . An enzyme cascade enables production of therapeutic oligonucleotides in a single operation. Science. 2023; 380(6650):1150-1154. DOI: 10.1126/science.add5892. View

4.
Palluk S, Arlow D, de Rond T, Barthel S, Kang J, Bector R . De novo DNA synthesis using polymerase-nucleotide conjugates. Nat Biotechnol. 2018; 36(7):645-650. DOI: 10.1038/nbt.4173. View

5.
Flamme M, Hanlon S, Marzuoli I, Puntener K, Sladojevich F, Hollenstein M . Evaluation of 3'-phosphate as a transient protecting group for controlled enzymatic synthesis of DNA and XNA oligonucleotides. Commun Chem. 2023; 5(1):68. PMC: 9814670. DOI: 10.1038/s42004-022-00685-5. View