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

Chemical nucleases.

J A Cowan1

  • 1Evans Laboratory of Chemistry, The Ohio State University, 100 West 18th Avenue, Columbus, Ohio 43210, USA. cowan@chemistry.ohio-state.edu

Current Opinion in Chemical Biology
|December 12, 2001
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

Structural and sequence basis for substrate selection in the cellular trafficking of Fe-S clusters, hemes and glutathione-complexed metals through membrane transporters.

Journal of inorganic biochemistry·2025
Same author

Understanding the Thermodynamics of Magnesium Binding to RNA Structural Motifs.

Life (Basel, Switzerland)·2024
Same author

Influence of the Weak Nuclear Force on Metal-Promoted Autocatalytic Strecker Synthesis of Amino Acids: Formation of a Chiral Pool of Precursors for Prebiotic Peptide and Protein Synthesis.

Life (Basel, Switzerland)·2024
Same author

Activity and Synergy of Cu-ATCUN Antimicrobial Peptides.

International journal of molecular sciences·2022
Same author

Structures of Atm1 provide insight into [2Fe-2S] cluster export from mitochondria.

Nature communications·2022
Same author

Spectroscopic and functional characterization of the [2Fe-2S] scaffold protein Nfu from Synechocystis PCC6803.

Biochimie·2021
Same journal

Function through shape: An overview of DNA G-quadruplexes in transcriptional regulation.

Current opinion in chemical biology·2026
Same journal

Advances in tools and technologies for multiplexed bioluminescence imaging.

Current opinion in chemical biology·2026
Same journal

High-resolution molecular mapping by expansion-coupled label-free and multimodal imaging.

Current opinion in chemical biology·2026
Same journal

Recent advances in glycoconjugate-based therapeutics.

Current opinion in chemical biology·2026
Same journal

Towards better red emitters for bioimaging: Innovations in rhodamine and cyanine chemistry.

Current opinion in chemical biology·2026
Same journal

Chemigenetic fluorescent biosensors in biological imaging - New trends and advances.

Current opinion in chemical biology·2026
See all related articles

Researchers are synthesizing functional mimics of metallonuclease enzymes for DNA and RNA cleavage. Ligand design improvements enhance substrate binding and catalytic activity, paving the way for targeted molecular recognition and cleavage applications.

Area of Science:

  • Biomimetic chemistry
  • Catalysis
  • Molecular biology

Background:

  • Metallonuclease enzymes play crucial roles in nucleic acid metabolism.
  • Developing synthetic mimics offers insights into enzyme mechanisms and potential therapeutic applications.
  • Current synthetic metallonucleases show promise but require further optimization for efficiency and selectivity.

Purpose of the Study:

  • To review recent advancements in the synthesis of functional metallonuclease mimics.
  • To highlight improvements in ligand design for enhanced catalytic activity and substrate binding.
  • To discuss progress in achieving site-selective cleavage of DNA and RNA.

Main Methods:

  • Synthesis of novel metal complexes with tailored ligand environments.
  • Investigation of catalytic activity in DNA and RNA cleavage reactions.

Related Experiment Videos

  • Structure-activity relationship studies to understand molecular determinants of selectivity.
  • Main Results:

    • Demonstrated successful synthesis of functional metallonuclease mimics.
    • Achieved significant improvements in catalytic rates compared to previous designs.
    • Reported successful double-strand DNA cleavage under hydrolytic conditions.
    • Identified key molecular factors for site-selective RNA cleavage.

    Conclusions:

    • Substantial progress has been made in developing synthetic metallonuclease mimics.
    • Ligand design is critical for optimizing substrate binding, complex stability, and catalytic efficiency.
    • Future research will focus on further enhancing activity and achieving precise site-selective cleavage for therapeutic and diagnostic applications.