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Related Concept Videos

Protein Complex Assembly02:41

Protein Complex Assembly

Proteins can form homomeric complexes with another unit of the same protein or heteromeric complexes with different types.  Most protein complexes self-assemble spontaneously via ordered pathways, while some proteins need assembly factors that guide their proper assembly. Despite the crowded intracellular environment, proteins usually interact with their correct partners and form functional complexes.
Many viruses self-assemble into a fully functional unit using the infected host cell to...
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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Updated: Jun 15, 2026

DNAzyme 10-23 - Based Nanomachines for Nucleic Acid Recognition
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DNA self-assembly for nanomedicine.

Rahul Chhabra1, Jaswinder Sharma, Yan Liu

  • 1Department of Chemistry and Biochemistry, Arizona State University, Tempe, AZ 85287, USA.

Advanced Drug Delivery Reviews
|March 17, 2010
PubMed
Summary

DNA nanostructures self-assemble into complex patterns, acting as molecular pegboards. These DNA systems are vital for precise molecular positioning in sensing, drug delivery, and constructing protein and nanoparticle arrays.

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Area of Science:

  • Nanotechnology and Supramolecular Chemistry
  • Biomolecular Engineering

Background:

  • Rational design of DNA branch junction molecules enables self-assembly of complex DNA nanostructures.
  • DNA nanostructures serve as versatile scaffolds for precise molecular organization.

Purpose of the Study:

  • To review recent advancements in self-assembled DNA nanostructural systems.
  • To summarize biomedical applications of information-guided DNA nanostructures.
  • To illustrate the use of DNA nanostructures in sensing, computation, drug delivery, and constructing molecular arrays.

Main Methods:

  • Exploration of rationally designed DNA branch junction molecules for self-assembly.
  • Review of state-of-the-art developments in DNA nanostructural systems.
  • Analysis of biomedical applications and use as scaffolds for molecular arrays.

Main Results:

  • Demonstrated construction of patterned supramolecular structures with high complexity.
  • Highlighted the utility of DNA tiles as molecular pegboards for deterministic positioning.
  • Illustrated applications in sensing, computation, drug delivery, and protein/nanoparticle arrays.

Conclusions:

  • Self-assembled DNA nanostructures offer precise control over molecular positioning and architectural design.
  • DNA nanostructures are promising platforms for diverse biomedical and nanotechnology applications.
  • Complex DNA architectures enable the creation of ordered arrays of proteins and nanoparticles.