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Related Concept Videos

Nucleic Acid Structure01:25

Nucleic Acid Structure

The pentose sugar in DNA is deoxyribose, while in RNA the pentose sugar is ribose. The difference between the sugars is the presence of the hydroxyl group on the ribose's second carbon and a hydrogen on the deoxyribose's second carbon. The phosphate residue attaches to the hydroxyl group of the 5′ carbon of one sugar and the hydroxyl group of the 3′ carbon of the sugar of the next nucleotide, which forms  a 5′ to 3′ phosphodiester linkage.
DNA Structure
DNA has a double-helix structure. The...
Nucleic acids02:43

Nucleic acids

Nucleic acids are the most important macromolecules for the continuity of life. They carry the cell's genetic blueprint and carry instructions for its functioning.
DNA and RNA
The two main types of nucleic acids are deoxyribonucleic acid (DNA) and ribonucleic acid (RNA). DNA is the genetic material in all living organisms, ranging from single-celled bacteria to multicellular mammals. It is in the nucleus of eukaryotes and in the organelles, chloroplasts, and mitochondria. In prokaryotes, the...

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DNA Origami-Mediated Substrate Nanopatterning of Inorganic Structures for Sensing Applications
08:59

DNA Origami-Mediated Substrate Nanopatterning of Inorganic Structures for Sensing Applications

Published on: September 27, 2019

Temperature-activated nucleic acid nanostructures.

Ke Zhang1, Xiao Zhu, Fei Jia

  • 1Department of Chemistry and Chemical Biology, Northeastern University , 360 Huntington Ave, Boston, Massachusetts 02115, United States.

Journal of the American Chemical Society
|September 13, 2013
PubMed
Summary
This summary is machine-generated.

Researchers developed temperature-responsive DNA-polymer hybrid nanoparticles. Heating exposes DNA for hybridization and biotin accessibility, while cooling blocks these functions, enabling controllable surface chemistry.

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Area of Science:

  • Nanotechnology
  • Materials Science
  • Biochemistry

Background:

  • Gold nanoparticles (AuNPs) are versatile platforms for various applications.
  • Poly(N-isopropylacrylamide) (PNIPAM) exhibits temperature-dependent solubility.
  • DNA nanotechnology offers precise control over molecular assembly and function.

Purpose of the Study:

  • To co-assemble DNA and PNIPAM onto gold nanoparticles.
  • To create a temperature-responsive system for controlling DNA accessibility and surface chemistry.
  • To demonstrate the on-off switching of surface function based on temperature cues.

Main Methods:

  • Co-assembly of DNA and PNIPAM onto gold nanoparticles.
  • Utilizing temperature changes (around 30 °C) to induce conformational changes in PNIPAM.
  • Monitoring DNA hybridization and biotin accessibility using complementary strands and temperature shifts.

Main Results:

  • Successful co-assembly of DNA and PNIPAM on gold nanoparticles.
  • Reversible exposure and hiding of DNA sequences in response to temperature.
  • Demonstrated on-off switching of surface chemistry, with DNA hybridization and biotin accessibility activated upon heating and blocked upon cooling.

Conclusions:

  • The developed DNA-PNIPAM-gold nanoparticle system provides a novel temperature-triggered platform.
  • This system allows for precise control over surface chemistry and function.
  • Potential applications in drug delivery, sensing, and responsive materials are suggested.