Programmable DNA Interstrand Crosslinking by Alkene–Alkyne [2 + 2] Photocycloaddition

• Published in: Journal of the American Chemical Society Vol. 145; no. 17; pp. 9428 - 9433
• Main Authors: Neitz, Hermann, Bessi, Irene, Kuper, Jochen, Kisker, Caroline, Höbartner, Claudia
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 03-05-2023
• Subjects: Base Pairing; Cross-Linking Reagents - chemistry; DNA - chemistry; Metals; Nucleic Acid Conformation; Nucleosides
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/jacs.3c01611

Covalent crosslinking of DNA strands provides a useful tool for medical, biochemical, and DNA nanotechnology applications. Here we present a light-induced interstrand DNA crosslinking reaction using the modified nucleoside 5-phenylethynyl-2′-deoxyuridine (PhedU). The crosslinking ability of PhedU was programmed by base pairing and by metal ion interaction at the Watson–Crick base pairing site. Rotation to intrahelical positions was favored by hydrophobic stacking and enabled an unexpected photochemical alkene–alkyne [2 + 2] cycloaddition within the DNA duplex, resulting in efficient formation of a PhedU dimer after short irradiation times of a few seconds. A PhedU-dimer-containing DNA was shown to efficiently bind a helicase complex, but the covalent crosslink completely prevented DNA unwinding, suggesting possible applications in biochemistry or structural biology.