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

Orthogonal base pairs continue to evolve.

Donald E Bergstrom1

  • 1Department of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, Indiana 47907, USA.

Chemistry & Biology
|April 29, 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

Nucleic Acid Binding Molecules.

Current protocols in nucleic acid chemistry·2022
Same author

Novel, Self-Assembling Dimeric Inhibitors of Human β Tryptase.

Journal of medicinal chemistry·2020
Same author

A Novel, Nonpeptidic, Orally Active Bivalent Inhibitor of Human β-Tryptase.

Pharmacology·2018
Same author

Target-Directed Self-Assembly of Homodimeric Drugs Against β-Tryptase.

ACS medicinal chemistry letters·2018
Same author

Reversible linkage of two distinct small molecule inhibitors of Myc generates a dimeric inhibitor with improved potency that is active in myc over-expressing cancer cell lines.

PloS one·2015
Same author

4-Aminocyclopentane-1,3-diols as platforms for diversity: synthesis of anandamide analogs.

Medicinal chemistry (Shariqah (United Arab Emirates))·2012
Same journal

The Hedgehog Pathway Effector Smoothened Exhibits Signaling Competency in the Absence of Ciliary Accumulation.

Chemistry & biology·2017
Same journal

DIVERSE System: De Novo Creation of Peptide Tags for Non-enzymatic Covalent Labeling by In Vitro Evolution for Protein Imaging Inside Living Cells.

Chemistry & biology·2015
Same journal

Differential Regulation of Specific Sphingolipids in Colon Cancer Cells during Staurosporine-Induced Apoptosis.

Chemistry & biology·2015
Same journal

Synthetic Peptides as cGMP-Independent Activators of cGMP-Dependent Protein Kinase Iα.

Chemistry & biology·2015
Same journal

Unraveling the B. pseudomallei Heptokinase WcbL: From Structure to Drug Discovery.

Chemistry & biology·2015
Same journal

Vitamin C as Cancer Destroyer, Investigating Sulfhydration, and the Variability in CFTR Interactome.

Chemistry & biology·2015
See all related articles

Researchers developed a novel orthogonal base pair for site-specific RNA modification. This breakthrough enables the introduction of photo-crosslinkable bases into RNA using T7 RNA polymerase transcription.

Area of Science:

  • Synthetic biology
  • Molecular biology
  • Biochemistry

Background:

  • The creation of unnatural base pairs (UBPs) is crucial for expanding the functional capabilities of nucleic acids.
  • Site-specific incorporation of modified nucleobases into RNA is challenging but essential for various applications.

Discussion:

  • A new orthogonal base pair has been synthesized and characterized.
  • This UBP allows for the specific insertion of a photo-crosslinkable modified base into RNA molecules.
  • The incorporation is achieved via T7 RNA polymerase-mediated transcription of DNA containing the complementary UBP partner.

Key Insights:

  • Demonstrates a novel method for site-specific RNA functionalization.
  • Enables the precise placement of photo-crosslinkable probes within RNA structures.

Related Experiment Videos

  • Expands the toolkit for creating engineered RNA molecules with tailored properties.
  • Outlook:

    • Potential applications in RNA structural biology, drug discovery, and diagnostics.
    • Further development of UBP systems for in vivo RNA engineering.
    • Integration of this technology into automated RNA synthesis platforms.