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Related Concept Videos

Protein Complex Assembly02:41

Protein Complex Assembly

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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...
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The nucleoid represents a structurally and functionally distinct region within prokaryotic cells, where the cell's DNA and associated proteins are housed. Unlike eukaryotic cells, prokaryotes lack a membrane-bound nucleus, and the nucleoid facilitates the organization and accessibility of the genetic material within this constraint. The DNA in most bacteria and archaea exists as a single, circular, double-stranded molecule that is highly compacted through supercoiling and interactions with...
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Related Experiment Video

Updated: Mar 16, 2026

Folding and Characterization of a Bio-responsive Robot from DNA Origami
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Folding and Characterization of a Bio-responsive Robot from DNA Origami

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Self-organized architectures from assorted DNA-framed nanoparticles.

Wenyan Liu1, Jonathan Halverson1, Ye Tian1

  • 1Center for Functional Nanomaterials, Brookhaven National Laboratory, Upton, New York 11973, USA.

Nature Chemistry
|August 25, 2016
PubMed
Summary
This summary is machine-generated.

Scientists developed DNA-framed nanoparticles for advanced nanomanufacturing. This method allows the creation of complex nanoparticle structures with designed architectures without precise particle positioning.

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Area of Science:

  • Nanotechnology
  • Materials Science
  • Biotechnology

Background:

  • Self-assembly science has evolved from understanding natural organization to actively controlling it.
  • Achieving complex nanomanufacturing necessitates methods for designing nanoparticle architectures without dictating individual particle placement.

Purpose of the Study:

  • To introduce a novel self-assembly concept for creating designed nanoparticle structures.
  • To demonstrate the fabrication of nanoparticle architectures using embedded building instructions via DNA frames.

Main Methods:

  • Integration of nanoparticles (NPs) with DNA origami frames to impart anisotropic and selective interactions.
  • Utilizing a set of distinct DNA-framed NPs with pre-defined topological types.

Main Results:

  • Successful fabrication of diverse planar nanoparticle architectures, including periodic structures and shaped meso-objects.
  • Demonstrated spontaneous emergence of complex shapes upon mixing different topological types of DNA-framed NPs.
  • Achieved self-assembly of non-trivial shapes, exemplified by a nanoscale model of the Vitruvian Man.

Conclusions:

  • DNA-framed nanoparticles offer a powerful platform for programmable self-assembly.
  • This approach enables the design and fabrication of complex nanoparticle architectures with high fidelity.
  • The methodology holds significant potential for advancing nanomanufacturing capabilities.