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Related Concept Videos

Chromatin Packaging01:32

Chromatin Packaging

16.5K
Each human somatic cell contains 6 billion base pairs of DNA. Each base pair is 0.34 nm long, meaning each diploid cell contains a staggering 2 meters of DNA. This long DNA strand is packed inside a nucleus measuring only 10-20 microns in diameter with the help of specialized DNA-binding proteins called histones. Together they form a compact DNA-protein complex called chromatin. The chromatin is further compacted into higher-order structures. The highest level of compaction is achieved during...
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Updated: May 17, 2025

Simple, Affordable, and Modular Patterning of Cells using DNA
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Simple, Affordable, and Modular Patterning of Cells using DNA

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Macroscale-area patterning of three-dimensional DNA-programmable frameworks.

Feiyue Teng1, Honghu Zhang2, Dmytro Nykypanchuk1

  • 1Center for Functional Nanomaterials, Brookhaven National Laboratory, Upton, NY, USA.

Nature Communications
|April 4, 2025
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Summary
This summary is machine-generated.

Researchers developed a method to grow 3D DNA origami superlattices on patterned surfaces. This advance enables precise nanoscale material assembly over large areas, bridging self-assembly with nanofabrication.

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Area of Science:

  • Nanotechnology
  • Materials Science
  • Biomolecular Engineering

Background:

  • DNA's adaptable structure enables programming of 3D nanostructures with nanoscale components.
  • Integrating self-assembled DNA lattices onto planar substrates is crucial for applications.
  • Existing methods require advancement for large-scale, patterned integration.

Purpose of the Study:

  • To develop an approach for growing 3D DNA-programmable frameworks on patterned silicon wafers and metal oxide surfaces.
  • To investigate factors influencing the growth and orientation of DNA superlattices on surfaces.
  • To enable the integration of self-assembled nanostructures with traditional nanofabrication.

Main Methods:

  • Utilizing polymer templates patterned by electron-beam lithography to guide growth.
  • Achieving selective growth of DNA origami superlattices on customized surface patterns.
  • Analyzing the correlation between assembly conditions and resulting superlattice characteristics.

Main Results:

  • Demonstrated selective growth of DNA origami superlattices into patterned areas with micron-scale features over macroscale regions.
  • Identified correlations between assembly conditions and superlattice orientation, domain size, twinning, and surface coverage.
  • Successfully integrated 3D DNA nanostructures onto diverse substrates.

Conclusions:

  • The developed approach bridges DNA self-assembly with top-down nanofabrication.
  • Enables the creation of engineered 3D nanoscale materials over macroscopic areas with precise control.
  • Opens possibilities for advanced applications requiring patterned, large-area nanoscale architectures.