ArticleJournal of the American Chemical Society2008
Coupling across a DNA helical turn yields a hybrid DNA/organic catenane doubly tailed with functional termini.
Article in Journal of the American Chemical Society, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
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Who cites it
13 citing papers in PubMed.
- Control of Solid-Supported Intra- vs Interstrand Stille Coupling Reactions for Synthesis of DNA-Oligophenylene Conjugates.Bioconjugate chemistry · 2024Article
- Terminal hairpin in oligonucleotide dominantly prioritizes intramolecular cyclization by T4 ligase over intermolecular polymerization: an exclusive methodology for producing ssDNA rings.Nucleic acids research · 2018Article
- Structural optimization of pseudorotaxane-forming oligonucleotides for efficient and stable complex formation.Nucleic acids research · 2018Article
- Cyclization of secondarily structured oligonucleotides to single-stranded rings by usingRSC advances · 2018Article
- Solid Phase Stepwise Synthesis of Polyethylene Glycols.Chemistry (Weinheim an der Bergstrasse, Germany) · 2017Article
- Highly efficient preparation of single-stranded DNA rings by T4 ligase at abnormally low Mg(II) concentration.Nucleic acids research · 2017Article
- Pseudorotaxane formation via the slippage process with chemically cyclized oligonucleotides.Nucleic acids research · 2017Article
- Artificial Molecular Machines.Chemical reviews · 2015Review
- Linking two DNA duplexes with a rigid linker for DNA nanotechnology.Nucleic acids research · 2015Article
- Site-specific inter-strand cross-links of DNA duplexes.Chemical science · 2013Article
- Powering the programmed nanostructure and function of gold nanoparticles with catenated DNA machines.Nature communications · 2013Article
- Templated synthesis of nylon nucleic acids and characterization by nuclease digestion.Chemical science · 2012Article
- Distance dependent interhelical couplings of organic rods incorporated in DNA 4-helix bundles.Bioconjugate chemistry · 2009Article
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Authors and funding
7 authors.
Funding
Abstract
We describe the synthesis of a hybrid DNA/organic macrocycle that is prepared by formation of an amide linkage across one full turn of DNA. Formation of a catenane proved that the linkage crossed a turn rather than running along the phosphodiester backbone contour. The product, a doubly tailed catenane, contains 5'- and 3'-termini that can be functionalized further or used to incorporate the catenane structure into other DNA assemblies.
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