Citation:
Chemistry. 2025 Mar 24:e202500448. doi: 10.1002/chem.202500448. Epub ahead of print. PMID: 40127302
Abstract:
Amino-modifiers are pivotal chemical modifications in nucleic acid scaffolds, serving applications ranging from (bio)conjugation to probing the origins of life. We report a simple, efficient, and cost-effective methodology for the introduction of amino-modifiers into DNA and RNA. This approach leverages a commercially available sulfonyl-containing solid support, which is first converted into a mixed N-hydroxysuccinimide carbonate, enabling robust conjugation with primary and secondary amines whether nucleosidic or non-nucleosidic. Oligonucleotides are synthesized via solid-phase synthesis and purified using standard methods, with little to no modification. Building on this framework, we introduce a novel amino-containing tandem oligonucleotide synthesis (aTOS) methodology, which facilitates the introduction of multiple terminal amino (or monophosphate) groups across two oligonucleotide strands. This innovative method broadens the toolkit for the introduction of amino modifications in nucleic acids, for applications in nucleic acid (bio)chemistry and biotechnology.
Epub:
Not Epub
Link to Publication:
https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/chem.202500448
Organism or Cell Type:
None
Delivery Method:
None