A Proximity-Based Programmable DNA Nanoscale Assembly Line
By Hongzhou Gu, J. Chao, S. Xiao, Nadrian C. Seeman. Nature, 2010
730 citations recorded by the source corpus.
Our ability to synthesize nanometre-scale chemical species, such as nanoparticles with desired shapes and compositions, offers the exciting prospect of generating new functional materials and devices by combining them in a controlled fashion into larger structures. Self-assembly can achieve this task efficiently, but may be subject to thermodynamic and kinetic limitations: reactants, intermediates and products may collide with each other throughout the assembly time course to produce non-target species instead of target species. An alternative approach to nanoscale assembly uses information-containing molecules such as DNA to control interactions and thereby minimize unwanted cross-talk between different components. In principle, this method should allow the stepwise and programmed construction of target products by linking individually selected nanoscale components—much as an automobile is built on an assembly line. Here we demonstrate that a nanoscale assembly line can be realized by the judicious combination of three known DNA-based modules: a DNA origami tile that provides a framework and track for the assembly process, cassettes containing three independently controlled two-state DNA machines that serve as programmable cargo-donating devices and are attached in series to the tile, and a DNA walker that can move on the track from device to device and collect cargo. As the walker traverses the pathway prescribed by the origami tile track, it sequentially encounters the three DNA devices, each of which can be independently switched between an ‘ON’ state, allowing its cargo to be transferred to the walker, and an ‘OFF’ state, in which no transfer occurs. We use three different types of gold nanoparticle species as cargo and show that the experimental system does indeed allow the controlled fabrication of the eight different products that can be obtained with three two-state devices.
Subfields: Mechanical Engineering, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/93e72171af1d6ce5aea1057a1d03743774e266dd
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Mechanical Engineering
In Molecular Biology
- Georg Seelig
- David Y. Zhang
- Matthew R. Jones
- Chad A. Mirkin
- Nadrian C. Seeman
- Chunhai Fan
- Juewen Liu
- Peixuan Guo
Citations in the corpus
- Morphing in nature and beyond: a review of natural and synthetic shape-changing materials and mechanisms (2016, background): “Hydrogels have been developed that selectively contract when exposed to specific antigens [136] and single strands of DNA [137], the latter with measurable difference in response to only one base change.”
- Self-assembled multivalent DNA nanostructures for noninvasive intracellular delivery of immunostimulatory CpG oligonucleotides. (2011, background): “3 Since the pioneering work of Seeman in the 1980s, there have been great advances in the area of DNA nanotechnology, in both directed assembly of highly complex nanostructures(4) 10 and promising applications of these nanostructures in molecular sensing,(11) 13 computation,(14,15) and nanomachines.”
- Dynamic DNA nanotechnology using strand-displacement reactions. (2011, background): “Since then, DNA origami technology [44] has enabled the construction of significantly longer tracks with more complex geometry [50, 96] leading to correspondingly longer processive walks and integration of multiple different kinds of DNA nanomotors.”
- Building plasmonic nanostructures with DNA. (2011, neutral): “DNA origami also provides an efficient template for organizing metallic nanoparticles into discrete multimeric plasmonic molecule”
- Programmable materials and the nature of the DNA bond (2015, methodology): “This has facilitated the demonstration of DNA walkers that can pick up nanoscale cargo (35), studies of distance-dependent bivalent ligandprotein binding (55), and the controlled placement of nanoparticles for plasmonic applications (56, 57).”