< Biomod | 2013 | Komaba
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|-|== Background of Project == | |
|-|: There were many previous studies related to the spontaneous activity of Biomolecule about Kinesin, which is a class of motor proteins, and walking DNA robots.But genuine nano-scale DNA motors which rotate at the stable speed were not yet created. | |
|-|: We tried to create the DNA screw system to overcome these issues in the present study. | |
|-|: The rotation system is used to create the complex motion with any devices, such as drills, screws and clocks.Therefore we thought that the nano-scale rotation system enables us to extended the future of DNA engineering. | |
|-|: The DNA screw has many strong points.DNA screw is able to embed in any other DNA structures and to be assembled into more complex structure easily, because we can take engineering approaches to make DNA structures.And, the size of structure can be easily scaled. In addition, DNA is a stable material than protein and can be used in various environments (ex. Temperature, pH and salt-density). | |
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Overview == |+|
|-|: The motor made in this project comprises three parts, including the cylinder as an axis, DNA Spiders as a source of power and the ring which actually rotate. At the first phase in the project, we design each parts and confirm their suitability for the motor by experiment. Then, in the second phase, we develop a method to combine each pasts and make up the motor. |+|
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|-|: If you need details of each experiment, please click ">>read more" link and jump to Design page. |+|
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|-|===== (Phase 1) ===== |+|
|-|=== Cylinder === |+|
|-|: The cylinder is put in the center of the motor as an axis supporting the rotation. The material DNA is formed into a cylindrical shape using DNA Origami technology. [[ Biomod/2013/Komaba/Design#Cylinder|>>read more]] |+|
|-|=== DNA Walker === |+|
The sources of power in rotational motion is DNA Spiders. DNA Spider consists of three DNA Walker which moves on footing by taking strands after another with DNAzyme. As they orbit the cylinder, their rotational movement is transmitted to DNA Ring. [[Biomod/2013/Komaba/Design#DNA_Walker|>>read more]] |+|
|-|=== Rotary Ring === |+|
|-|: It is the DNA ring part that actually rotates. It has shape like the side surface of a disk, and is also composed with DNA Origami technology. [[Biomod/2013/Komaba/Design#Rotary_Ring|>>read more]] |+|
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=== (Phase 2) ===== |+|
|-|=== Motor === |+|
The motor is realized by assembling above thee parts: Cylinder, Spider, Ring. Unlike motors in electrical work, rotary parts of our motor is outer ones and the central cylinder are fixed. [[Biomod/2013/Komaba/Design#Cylinder_Motor_( Combination_of_above_parts) |>>read more]] |+|
of our is (). the . to and
|-|=== Another Structure === |+|
|-|: The motor made in this project rotates by DNA spider and round footings. In this system, the cylinder become too long if motor make many revolutions. However, we have an idea which make it possible to make lasting rotation by using long straight footing and DNA spiders positioned circularly. |+|
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|-|== Vision for the future( Phase ∞) == |+|
|-|=== DNA submarine === |+|
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|-|=== Gear Connecting === |+|
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|-|=== DNA pore-forming === |+|
|-|If this DNA screw is realized, it would be possible to make a hole on the surface of a vesicle like rotating a screw by connecting the ring to a vesicle with cholesterol. |+|
, . DNA()
|-|=== DNA Clocks === |+|
|-|DNAスパイダーの数を増やしてリングの回転速度を安定させることで、時計のように一定間隔の時間を計ることができると考えます( 日本語変だから、なんかいいのあったら変えて＞＜) 。これは電子コンピュータにおけるクロックの役割を果たすことができ、DNAコンピューティング技術の発展に貢献できるとかんがえます。 |+|
Background of Project
Many kinds of active biomolecules such a kinesin and DNA walkers which are a class of motor proteins and artificial chemical devices have been studied, and their features inspired biomimetics, a large research area aiming at mimicking organism to design novel materials. One of the aims of biomimetics is to create motors by using recent DNA synthesis technologies. We challenged to design a DNA-based rotational structure, named “DNA screw.” Because genuine nano-scale rotating DNA motors are not yet demonstrated, designing such motors is a challenging subject. This structure consists of a small cylinder inside a large ring, which are connected by DNA strands. Since our structure is made of DNA, combining other existing DNA structures is feasible.
Process of the making DNA screw
The key components of DNA screw are three; A cylinder, a ring, and DNA spider. In addition, to visually see how the spider actually move, simulation is also an important factor of our project.
Vision for the future
First of all, our DNA screw is designed to be appled to phage-like functional structure(Figure P2). Phages make pores on the cellular surface and inject DNA or RNA genome inside cells. It has to be researched on what way the structure attaches to the surface and makes pores
In addition, one of our project’s applications is a suspension rod(Figure P3). Let’s imagine a pointer used in class lectures. The rod contains many cylinders and can extend and shrink by changing a relative distance of each cylinder. Inner cylinder corresponds to the DNA cylinder and outer one does to the DNA ring in our project. The rod stretching can be controlled by ordering DNA strands. For example, the rod, which has zigzag-placed strands in parallel to the cylinder's axis, can shrink and suspend spontaneously.
By using suspending movement, our DNA screw can act as a biophysical sensor which measures kinetic properties. For example, DNA screw can be applied to unfolding proteins. The cylinder is attached to a protein, the ring stretches protein’s one end.
Furthermore, this DNA suspension rod can provide a dynamical creating methodology for large micro-scale structures from nano-scale objects such as DNA tensegrity by Liedl et al. (2010). We assume that our DNA cylinders can function as strings and rod-shape structures such as carbon nanotube can work as rods. This method contains three steps. First, combining DNA cylinders and nano rods. Second, starting DNA spiders' movements and reaching a maximum-strength state. Third, cutting connections between DNA cylinders and nano rods and discomposing a large tensegrity structure.
Tim Liedl, Björn Högberg, Jessica Tytell, Donald E. Ingber, and William M. Shih, Self-assembly of 3D prestressed tensegrity structures from DNA. Nat Nanotechnol. 2010 July ; 5(7): 520–524.