Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

A second-generation copper(II)-mediated metallo-DNA-base pair.

Nicole Zimmermann1, Eric Meggers, Peter G Schultz

  • 1Department of Chemistry, The Scripps Research Institute, La Jolla, CA 92037, USA.

Bioorganic Chemistry
|January 1, 2004
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Imidazol-2-ylidene-Based NCCN Ligands for Chiral-at-Iron Catalysis.

Organometallics·2026
Same author

Asymmetric Iron-Catalyzed Vicinal C(sp<sup>3</sup>)─H Diamination of Carboxylic Acids.

Angewandte Chemie (International ed. in English)·2026
Same author

Teaching interprofessional competency in graduate education and training - implementation and evaluation of a case-based, interprofessional online seminar for pharmacists and physicians specializing in general practice.

GMS journal for medical education·2026
Same author

An Achiral Tetradentate Cis-α-Coordinating NCCN Ligand Gives Rise to a Configurationally Stable Chiral-at-Iron Complex for Enantioselective Catalysis.

Chemistry (Weinheim an der Bergstrasse, Germany)·2025
Same author

The β-lactamase inhibitor concentration-dependent minimum inhibitory concentration (MICcBLI) as methodology to assess the pharmacokinetic/pharmacodynamic relationship of piperacillin/tazobactam for dosing optimization.

The Journal of antimicrobial chemotherapy·2025
Same author

Antibiotic pharmacodynamics: from MIC to advanced metrics and their applications.

The Journal of antimicrobial chemotherapy·2025

Researchers developed a new metal-dependent base pair for DNA. This second-generation metallo-base pair offers enhanced stability and selectivity, enabling its use in DNA duplexes.

Area of Science:

  • Synthetic biology
  • Supramolecular chemistry
  • Nucleic acid chemistry

Background:

  • Metal-dependent pairing offers an alternative to natural DNA base pairing.
  • First-generation copper(II)-mediated metallo-base pairs (pyridine-2,6-dicarboxylate and pyridine) showed comparable stability to natural pairs but lacked selectivity.

Purpose of the Study:

  • To enhance the selectivity of metal-dependent base pairing.
  • To develop a second-generation metallo-base pair with improved stability and selectivity.
  • To assess the feasibility of incorporating multiple metallo-base pairs into DNA.

Main Methods:

  • Design and synthesis of a second-generation metallo-base pair using pyridine-2,6-dicarboxamide and pyridine.
  • Stability and selectivity assessment of the new metallo-base pair compared to natural base pairs.

Related Experiment Videos

  • Incorporation of multiple metallo-base pairs into DNA duplexes to evaluate structural integrity.
  • Main Results:

    • The second-generation metallo-base pair (pyridine-2,6-dicarboxamide and pyridine) demonstrated superior stability over natural dA:dT and dC:dG pairs.
    • This new metallo-base pair exhibited high selectivity, effectively preventing mispairing.
    • Stable DNA duplexes were formed with multiple incorporated metallo-base pairs, indicating successful replacement of hydrogen-bonding pairs.

    Conclusions:

    • A novel, highly stable, and selective metal-dependent base pair has been engineered.
    • Metallo-base pairs can effectively replace natural hydrogen-bonding base pairs at multiple sites within DNA structures.
    • This advancement opens possibilities for novel DNA architectures and functions.