Reciprocating devices are a common part of the macroscopic world. Examples of reciprocating machines are petrol and diesel engines or a hydraulic pump. At the core of these machines is a piston and cylinder assembly where the piston executes a reciprocating motion inside the cylinder. Reciprocating motion like that in a piston has not been available in a nanoscale machine until now. Ned Seeman and his team at New York University have designed a DNA device that exhibits reciprocal motion. They have used the PX-JX2 device, a robust sequence-dependent nanomechanical DNA machine, as the basis for constructing a pair of reciprocal devices, wherein one device assumes one state, while the other device assumes the opposite state.
Molecular-size motors have evolved in nature, where they are used in virtually every important biological process. In contrast, the development of synthetic nanomotors that mimic the function of these amazing natural systems and that could be used in man-made nanodevices is in its infancy. Building nanoscale motors is not just an exercise in scaling down the design of a macroworld engine to nanoscale dimensions. In addition to organic molecules, scientists increasingly are looking to DNA as a very promising way to fabricate nanomotors. The concept of a single DNA molecule nanomotor was already introduced in early 2002. However, this and subsequent designs require addition and removal of fuel and waste strands for motor function, although some artificial nanomotors can utilize alternative energy sources, including hydrolysis of the DNA backbone and ATP. Researchers at the University of Florida have now designed a photoswitchable single-molecule DNA nanomotor. It is the first fully reversible single-molecule DNA nanomachine driven by photons without any additional DNA strands as fuel.
Proteins that bind to specific sites of DNA are essential to all biological functions of DNA. These DNA-binding proteins include transcription factors which modulate the process of transcription, various polymerases, nucleases which cleave DNA molecules, and histones which are involved in chromosome packaging in the cell nucleus. Developing methods to precisely determine the locations and occupancy of DNA-binding proteins is instrumental to scientists' understanding of cellular processes like gene expression and regulation. Motivated by the desire to overcome some of the inherent limitations of existing biochemical techniques for mapping protein binding sites on DNA, scientists at UCLA have now demonstrated the viability of a single molecule approach to directly visualize and map protein binding sites on DNA using fluorescent quantum dots, allowing multicolor, nanometer-resolution localization.
Studies have already shown the complexity of architecture that is achievable using DNA as building blocks. For instance, nanofabrication via molecular self-assembly has already resulted in simple DNA polyhedra with connectivities of a cube, octahedron, and a tetrahedron. Platonic solids - any one of five solids whose faces are congruent regular polygons and whose polyhedral angles are all congruent - are the most efficient at enclosing large volumes. The more complex the polyhedron, the greater its ability to encapsulate cargo, because the capsule size can be maximized while keeping the pore-size of the capsule minimal. The most complex platonic solid is the icosahedron and therefore this would be most suitable for achieving cargo encapsulation. The DNA shell of such a capsule could protect vulnerable drugs from degradation by proteins until they reach their target site. It could also prevent dangerous drugs from leaking out until the capsule reaches its intended target. The DNA shell could also allow attachment to a protein that could ferry the drug-loaded capsule to a target.
DNA nanomachines - synthetic DNA assemblies that switch between defined molecular shapes upon stimulation by external triggers - can be controlled by a variety of methods; these include pH changes and the addition of other molecular components, such as small molecule effectors, proteins and DNA strands. A team of Indian researchers has now taken structural DNA nanotechnology, where so far only in vitro applications have been demonstrated, across a new boundary and into living systems. They describe the successful operation of an artificially designed DNA nanomachine inside living cells, and show that these nanomachines work as efficiently inside cells as in vitro. The device is externally triggered by protons and functions as a pH sensor based on fluorescence resonance energy transfer (FRET) inside living cells.
DNA, the fundamental building block of life, has become an intense nanotechnology research field. DNA molecules can serve as precisely controllable and programmable scaffolds for organizing functional nanomaterials in the design, fabrication, and characterization of nanoscale devices such as sensors and electronics. Most DNA research on controlled self-assembly deals with two-dimensional, i.e. flat, patterns and an expansion of these arrays into the third dimension has been challenging. New research coming out of UC Santa Barbara describes the self-assembly of multilayer hexagonal DNA arrays through highly regular interlayer packing. The researchers found that DNA arrays assembled into a two dimensional hexagonal pattern, or a sheet, assemble further into multilayer stacks.
DNA, the fundamental building block of our genetic makeup, has become an intense nanotechnology research field. DNA molecules can serve as precisely controllable and programmable scaffolds for organizing functional nanomaterials in the design, fabrication, and characterization of nanometer scale electronic devices and sensors. The reason why DNA could be useful in nanotechnology for the design of electric circuits is the fact that it actually is the best nanowire in existence - it self-assembles, it self-replicates and it can adopt various states and conformations. The most basic and simplest form of DNA mechanical devices that are expected to be the first to demonstrate some close-to-reality functions are DNA tweezers. This concept was first introduced in 2000 by scientists at Bell Labs and Oxford University. To keep this type of tweezers running, two fuel DNA strands are alternately added to a buffered solution that contains the tweezers. These fuels are basically two stretches of complementary DNA, one of which closes the tweezers and the other opens them. The exciting potential applications for DNA tweezers include their use in constructing various molecular devices dedicated to repairing a functional unit in a cell, harnessing the delivery of drug molecules to pathogenic cells, or assembling nanoscale devices.
In case you haven't seen the absolutely amazing animation 'Cellular Visions: The Inner Life of a Cell' yet, go watch it now. In it, there is a sequence where a motor protein is sort of 'walking' along a filament, dragging this round sphere of lipids behind it. This kind of nanoscale biological motor is able to load/unload particular types of cargo without external stimuli, and transport them along cytoskeletal filaments by using the energy of adenosine triphosphate (ATP) hydrolysis within cells. Nanotechnology researchers are fascinated by the various molecular delivery systems that have evolved in nature and they are receiving increasing attention as blueprints for nanoscale actuators and building blocks to construct artificially-engineered bio-hybrid systems. Some researchers expect that artificial molecular transport systems which utilize microtubules motility will be an alternative way to pressure-driven or electrokinetic flow-based microfluidic devices. Researchers in Japan propose a molecular transport system that can achieve autonomous loading/unloading of specified cargoes. This system loads a cargo molecule through DNA hybridization.