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Related Concept Videos

Ribozymes02:47

Ribozymes

The term ribozyme is used for RNA that can act as an enzyme. Ribozymes are mainly found in selected viruses, bacteria, plant organelles, and lower eukaryotes. Ribozymes were first discovered in 1982 when Tom Cech’s laboratory observed Group I introns acting as enzymes. This was shortly followed by the discovery of another ribozyme, Ribonulcease P, by Sid Altman’s laboratory. Both Cech and Altman received the Nobel Prize in chemistry in 1989 for their work on ribozymes.
Ribozymes can be...

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DNAzyme 10-23 - Based Nanomachines for Nucleic Acid Recognition
07:16

DNAzyme 10-23 - Based Nanomachines for Nucleic Acid Recognition

Published on: February 9, 2024

pH-programmable DNAzyme nanostructures.

Simcha Shimron1, Nimrod Magen, Johann Elbaz

  • 1Institute of Chemistry, The Hebrew University of Jerusalem, Jerusalem, Israel.

Chemical Communications (Cambridge, England)
|July 7, 2011
PubMed
Summary
This summary is machine-generated.

Engineered DNA nanostructures function as pH-switchable devices. These nanodevices control the activation and deactivation of DNAzymes that mimic horseradish peroxidase activity.

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Area of Science:

  • Biotechnology and Nanotechnology
  • Molecular Biology
  • Chemical Biology

Background:

  • DNA nanostructures offer precise control over molecular interactions.
  • DNAzymes with enzymatic activity, such as horseradish peroxidase (HRP) mimicry, are valuable tools.
  • Developing controllable systems for DNAzyme activity is crucial for advanced applications.

Purpose of the Study:

  • To design and characterize pH-switchable DNA nanostructures.
  • To utilize these nanostructures for the controlled activation and deactivation of HRP-mimicking DNAzymes.

Main Methods:

  • Engineering of two distinct DNA nanostructures: a nucleic acid functional hairpin and a DNA tweezers assembly.
  • Integration of these nanostructures with HRP-mimicking DNAzymes.
  • Investigation of the pH-dependent switching behavior of the DNA nanostructure-DNAzyme system.

Main Results:

  • Demonstrated that the engineered DNA nanostructures act as effective pH-switchable controllers.
  • Successfully achieved 'ON-OFF' regulation of the HRP-mimicking DNAzyme activity.
  • The system exhibits reversible switching in response to changes in pH.

Conclusions:

  • The developed DNA nanostructures provide a novel platform for creating responsive molecular devices.
  • This pH-switchable system enables precise temporal control over DNAzyme activity.
  • Potential applications in biosensing, diagnostics, and targeted drug delivery.