GSNT
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Controlling DNA Orientation Using a Brush
Professor Dong Ki Yoon’s research team in the Graduate School of Nanoscience and Technology has developed a technique for producing periodic DNA zigzag structures using a common make-up brush.
The results of the research, first-authored by Ph.D. student Yun Jeong Cha and published in Advanced Materials (online, November 15, 2016), has been highlighted in the hot topics of “Liquid Crystals.”
There exist various methods for synthesizing DNA-based nanostructures, but they commonly involved complex design processes and required expensive DNA samples with regulated base sequences.
Using DNA materials extracted from salmon, the research team was able to produce a nanostructure with a well-aligned zigzag pattern at one-thousandth of the usual cost.
The team used a commercial make-up brush bought at a cosmetics store, and with it, applied the salmon DNA in one direction onto a plate, in the same way paint is brushed onto paper. Using a brush with a width of several centimeters, the team aligned DNA molecules of 2 nanometers in diameter along the direction of the brush strokes.
As the thin and dense film of DNA came into contact with air, it lost moisture. An expansive force was created between the dried film and the plate. This force interacted with the elastic force of DNA and caused undulations in the uni-directionally aligned DNA molecules, which resulted in a regular zigzag pattern.
The zigzag DNA’s base sequences could not be controlled because it was extracted from biological sources. However, it has the advantage of being cheap and readily available without compromising its structural integrity and provides a very regular and intricate structure.
This kind of well-ordered DNA structure can be used as template because it can guide or control versatile guest functional materials that are applied to its surface. For example, it can align liquid crystals used in displays, as well as metallic particles and semi-conductors. It is expected that this capacity can be extended to optoelectric devices in the future.
Professor Yoon remarked that “these findings have special implications, as they have demonstrated that various materials in nature aside from DNA, such as proteins, muscle cells, and components of bones can be applied to optoelectric devices.”
This research has been carried out with the support of the Korea National Research Foundation’s Nanomaterials Fundamental Technology Development Program and the Pioneer Research Center under the High-tech Convergence Technology Development Program.
Source: "Control of Periodic Zigzag Structures of DNA by a Simple Shearing Method" by Yun Jeong Cha and Dong Ki Yoon (Advanced Materials, November 15, 2016, DOI: 10.1002/adma.201604247)
Figure 1. Diagram showing the well-ordered zigzag structure of DNA, and the internal molecular orientation
Figure 2. (Left) Unaligned DNA (Right) Aligned DNA after being brushed and dried
Figure 3. Control of the periodicity of the DNA zigzag patterns using micro-channel plates
Figure 4. Diagram representing the control of orientation of liquid crystal materials applied on a zigzag DNA template, and a polarized optical microscope image
2017.01.10 View 6486 -
Hierarchically-Porous Polymers with Fast Absorption
KAIST's Professor Myungeun Seo and his research team from the Graduate School of Nanoscience and Technology has developed a method to form micropores of less than 2 nanometers within porous polymers where 10 nanometers long mesopores connect like a net. The advantage of the porous polymers is fast absorption of molecules.
Porous polymers with micropores of less than 2 nanometers, like a zeolite, have a large surface area. They are used as a means to store hydrogen-based molecules or as a catalytic support that can be used as a surface to convert a material into a desired form. However, because the size of the pores in its path was too small for the molecules, it took a long time to spread into the pores and reach the surface.
To reach the surface efficiently, a lung cell or the vein of a leaf has a structure wherein the pores are subdivided into different sizes so that the molecule can spread throughout the organ. A technology that can create not only micropores but also bigger pores was necessary in order to create such structure.
The research team solved the issue by implementing a "self-assembly" of block polymers to easily form a net-like nanostructure from mesopores of 10 nanometers.
The team created hierarchically-porous polymers consisting of two different types of pores by using a hypercrosslinking reaction along with the "self-assembly" method. The reaction creates micropores within the chain after the polymer chain is confined by a chemical bond.
This porous polymer has micropores that are smaller than 2 nanometers on the walls of mesopores while 10 nanometers long mesopores forming 3-dimensional net structures. Because of the "self-assembly" method, the size of mesopores can be adjusted within the range of 6 to 15 nanometers.
This is the first case where a porous polymer has both well-defined mesopores and micropores. The research team verified the effect of hierarchically-porous structures on absorption of molecules by confirming that the porous polymer had faster absorption speeds than a polymer consisting only of micropores.
Professor Seo said, “The study has found a simple way to create different sizes of pores within a polymer.” He expected that the hierarchically-porous polymers can be used as a catalytic support in which fast diffusion of molecules is essential, or for molecule collection.
The research was sponsored by National Research Foundation of Korea and published online in the Journal of the American Chemical Society.
Figure 1 – Net-like Structure of Hierarchically-Porous Polymers with Mesopores and Micropores on the walls of Mesopores.
Figure 2 - Hierarchically-Porous Polymers
Figure 3 – Comparison of Porous-Polymers consisting of Mesopores only (left), and Mesopores and Micropores (right)
2015.01.13 View 8089 -
KAIST Develops Core Technology to Synthesize a Helical Nanostructure
Professor Dong-Ki Yoon’s research team of the Graduate School of Nanoscience and Technology (GSNT) at KAIST has developed helical nanostructures using self-assembly processes. The results were published in the Proceedings of the National Academy of Sciences of the United States of America(PNAS) on the October 7th.
This technology enables the synthesis of various helical structures on a relatively large confined area. Its synthesis is often considered the most arduous for three dimensional structures. Formed from liquid crystal, the structure holds a regular helical structure within the confined space of 20 to 300 nanometers. Also, the distance between each pattern increased as the diameter of the nanostructure increased.
Liquid crystals have a unique property of responding sensitively to the surrounding electromagnetic field. The technology, in combination with the electromagnetic property of liquid crystal, is expected to foster the development of highly efficient optoelectronic devices.
Using this technology, it is possible to develop three dimensional patterning technology beyond the current semiconductor manufacturing technology which uses two dimensional photolithography processes. Three-dimensional semiconductor devices are expected to store hundred times more data than current devices. They will also lower costs by simplifying manufacturing processes.
The essence of this research, “self-assembly in confined space,” refers to controlling complex nanostructures, which can be synthesized from materials such as macromolecules, liquid crystal molecules, and biomolecules in relation to surrounding environments including the temperature, concentration, and pH.
The research team produced a confined space with a length of tens of nanometers by using a porous anodized aluminum membrane induced from an electrochemical reaction. They successfully synthesized independently controlled helical nanostructures by forming the helical structures from liquid crystal molecules within that space.
Professor Yoon said, “This research examines the physicochemical principle of controlling helical nanostructures.” He highlighted the significance of the research and commented, “The technology enables the control of complex nanostructures from organic molecules by using confined space and surface reforming.”
He added that, “When grafted with nanotechnology or information technology, this technology will spur new growth to liquid crystal-related industries such as the LCD.”
The research was led by two Ph.D. candidates, Hanim Kim and Sunhee Lee, under the guidance of Professor Yoon. Dr. Tae-Joo Shin of the Pohang Accelerator Laboratory, Professor Sang-Bok Lee of the University of Maryland, and Professor Noel Clark of the University of Colorado also participated.
Picture 1. Electron Microscopy Pictures and Conceptual Diagrams of Helical Nanostructures
Picture 2. Electron Microscopy Pictures of Manufactured Helical Nanostructures
2014.10.29 View 8293