Showing posts with label molecules. Show all posts
Showing posts with label molecules. Show all posts

Wednesday, June 29, 2011

Largest biochemical circuit built out of small synthetic DNA molecules


Largest biochemical circuit built out of small synthetic DNA molecules

 


A wiring diagram specifying a system of 74 DNA molecules that constitute the largest synthetic circuit of its type ever made. The circuit computes the square root of a number up to 15 and rounds down to the nearest integer (the discrete square root of a four-bit integer). Credit: Caltech/Lulu Qian


In many ways, life is like a computer. An organism's genome is the software that tells the cellular and molecular machinery?the hardware?what to do. But instead of electronic circuitry, life relies on biochemical circuitry?complex networks of reactions and pathways that enable organisms to function. Now, researchers at the California Institute of Technology (Caltech) have built the most complex biochemical circuit ever created from scratch, made with DNA-based devices in a test tube that are analogous to the electronic transistors on a computer chip.


Engineering these allows researchers to explore the principles of information processing in biological systems, and to design biochemical pathways with decision-making capabilities. Such circuits would give biochemists unprecedented control in designing chemical reactions for applications in biological and chemical engineering and industries. For example, in the future a synthetic biochemical circuit could be introduced into a clinical blood sample, detect the levels of a variety of molecules in the sample, and integrate that information into a diagnosis of the pathology.


"We're trying to borrow the ideas that have had huge success in the electronic world, such as abstract representations of computing operations, programming languages, and compilers, and apply them to the biomolecular world," says Lulu Qian, a senior postdoctoral scholar in bioengineering at Caltech and lead author on a paper published in the June 3 issue of the journal Science.


Along with Erik Winfree, Caltech professor of computer science, computation and neural systems, and bioengineering, Qian used a new kind of DNA-based component to build the largest artificial biochemical circuit ever made. Previous lab-made biochemical circuits were limited because they worked less reliably and predictably when scaled to larger sizes, Qian explains. The likely reason behind this limitation is that such circuits need various molecular structures to implement different functions, making large systems more complicated and difficult to debug. The researchers' new approach, however, involves components that are simple, standardized, reliable, and scalable, meaning that even bigger and more complex circuits can be made and still work reliably.


"You can imagine that in the computer industry, you want to make better and better computers," Qian says. "This is our effort to do the same. We want to make better and better biochemical circuits that can do more sophisticated tasks, driving molecular devices to act on their environment."


To build their circuits, the researchers used pieces of DNA to make so-called logic gates?devices that produce on-off output signals in response to on-off input signals. Logic gates are the building blocks of the digital logic circuits that allow a computer to perform the right actions at the right time. In a conventional computer, logic gates are made with electronic transistors, which are wired together to form circuits on a silicon chip. Biochemical circuits, however, consist of molecules floating in a test tube of salt water. Instead of depending on electrons flowing in and out of transistors, DNA-based logic gates receive and produce molecules as signals. The molecular signals travel from one specific gate to another, connecting the circuit as if they were wires.


Winfree and his colleagues first built such a biochemical circuit in 2006. In this work, DNA signal molecules connected several DNA logic gates to each other, forming what's called a multilayered circuit. But this earlier circuit consisted of only 12 different DNA molecules, and the circuit slowed down by a few orders of magnitude when expanded from a single logic gate to a five-layered circuit. In their new design, Qian and Winfree have engineered logic gates that are simpler and more reliable, allowing them to make circuits at least five times larger.


Their new logic gates are made from pieces of either short, single-stranded DNA or partially double-stranded DNA in which single strands stick out like tails from the DNA's double helix. The single-stranded DNA molecules act as input and output signals that interact with the partially double-stranded ones.


"The molecules are just floating around in solution, bumping into each other from time to time," Winfree explains. "Occasionally, an incoming strand with the right DNA sequence will zip itself up to one strand while simultaneously unzipping another, releasing it into solution and allowing it to react with yet another strand." Because the researchers can encode whatever DNA sequence they want, they have full control over this process. "You have this programmable interaction," he says.


Qian and Winfree made several circuits with their approach, but the largest?containing 74 different DNA molecules?can compute the square root of any number up to 15 (technically speaking, any four-bit binary number) and round down the answer to the nearest integer. The researchers then monitor the concentrations of output molecules during the calculations to determine the answer. The calculation takes about 10 hours, so it won't replace your laptop anytime soon. But the purpose of these circuits isn't to compete with electronics; it's to give scientists logical control over biochemical processes.


Their circuits have several novel features, Qian says. Because reactions are never perfect?the molecules don't always bind properly, for instance?there's inherent noise in the system. This means the molecular signals are never entirely on or off, as would be the case for ideal binary logic. But the new logic gates are able to handle this noise by suppressing and amplifying signals?for example, boosting a signal that's at 80 percent, or inhibiting one that's at 10 percent, resulting in signals that are either close to 100 percent present or nonexistent.


All the logic gates have identical structures with different sequences. As a result, they can be standardized, so that the same types of components can be wired together to make any circuit you want. What's more, Qian says, you don't have to know anything about the behind the circuit to make one. If you want a circuit that, say, automatically diagnoses a disease, you just submit an abstract representation of the logic functions in your design to a compiler that the researchers provide online, which will then translate the design into the DNA components needed to build the circuit. In the future, an outside manufacturer can then make those parts and give you the circuit, ready to go.


The circuit components are also tunable. By adjusting the concentrations of the types of DNA, the researchers can change the functions of the logic gates. The circuits are versatile, featuring plug-and-play components that can be easily reconfigured to rewire the circuit. The simplicity of the also allows for more efficient techniques that synthesize them in parallel.


"Like Moore's Law for silicon electronics, which says that computers are growing exponentially smaller and more powerful every year, molecular systems developed with nanotechnology have been doubling in size roughly every three years," Winfree says. Qian adds, "The dream is that synthetic biochemical circuits will one day achieve complexities comparable to life itself."

Monday, February 14, 2011

What a ride! Researchers take molecules for a spin (w/ Video)


What a ride! Researchers take molecules for a spin (w/ Video)


Kolomeisky and Rice graduate student Alexey Akimov have taken a large step toward defining the behavior of these molecular whirligigs with a new paper in the American Chemical Society's Journal of Physical Chemistry C. Through molecular dynamics simulations, they defined the ground rules for the rotor motion of molecules attached to a gold surface.



"This is no cartoon. It's a real molecule, with all the interactions taking place correctly," said Anatoly Kolomeisky as he showed an animation of atoms twisting and turning about a central hub like a carnival ride gone mad.


Kolomeisky, a Rice University associate professor of chemistry, was offering a peek into a molecular midway where atoms dip, dive and soar according to a set of rules he is determined to decode.


Kolomeisky and Rice graduate student Alexey Akimov have taken a large step toward defining the behavior of these molecular whirligigs with a new paper in the American Chemical Society's Journal of Physical Chemistry C. Through molecular dynamics simulations, they defined the ground rules for the rotor motion of molecules attached to a gold surface.



You need Flash installed to watch this video


An animation of a rotor simulation

It's an extension of their work on Rice's famed nanocars, developed primarily in the lab of James Tour, Rice's T.T. and W.F. Chao Chair in Chemistry as well as a professor of mechanical engineering and materials science and of computer science, but for which Kolomeisky has also constructed molecular models.

Striking out in a different direction, the team has decoded several key characteristics of these tiny rotors, which could harbor clues to the ways in which molecular motors in human bodies work.


The motion they described is found everywhere in nature, Kolomeisky said. The most visible example is in the flagella of bacteria, which use a simple rotor motion to move. "When the flagella turn clockwise, the bacteria move forward. When they turn counterclockwise, they tumble." On an even smaller level, ATP-synthase, which is an enzyme important to the transfer of energy in the cells of all living things, exhibits similar rotor behavior -- a Nobel Prize-winning discovery.


Understanding how to build and control molecular rotors, especially in multiples, could lead to some interesting new materials in the continuing development of machines able to work at the nanoscale, he said. Kolomeisky foresees, for instance, radio filters that would let only a very finely tuned signal pass, depending on the nanorotors' frequency.


"It would be an extremely important, though expensive, material to make," he said. "But if I can create hundreds of rotors that move simultaneously under my control, I will be very happy."


The professor and his student cut the number of parameters in their computer simulation to a subset of those that most interested them, Kolomeisky said. The basic-model molecule had a sulfur atom in the middle, tightly bound to a pair of alkyl chains, like wings, that were able to spin freely when heated. The sulfur anchored the molecule to the gold surface.


While working on a previous paper with researchers at Tufts University, Kolomeisky and Akimov saw photographic evidence of rotor motion by scanning tunneling microscope images of sulfur/alkyl molecules heated on a gold surface. As the heat rose, the image went from linear to rectangular to hexagonal, indicating motion. What the pictures didn't indicate was why.


That's where computer modeling was invaluable, both on the Kolomeisky lab's own systems and through Rice's SUG@R platform, a shared supercomputer cluster. By testing various theoretical configurations -- some with two symmetrical chains, some asymmetrical, some with only one chain -- they were able to determine a set of interlocking characteristics that control the behavior of single-molecule rotors.


First, he said, the symmetry and structure of the gold surface material (of which several types were tested) has a lot of influence on a rotor's ability to overcome the energy barrier that keeps it from spinning all the time. When both arms are close to surface molecules (which repel), the barrier is large. But if one arm is over a space -- or hollow -- between gold atoms, the barrier is significantly smaller.


Second, symmetric rotors spin faster than asymmetric ones. The longer chain in an asymmetric pair takes more energy to get moving, and this causes an imbalance. In symmetric rotors, the chains, like rigid wings, compensate for each other as one wing dips into a hollow while the other rises over a surface molecule.


Third, Kolomeisky said, the nature of the chemical bond between the anchor and the chains determines the rotor's freedom to spin.


Finally, the chemical nature of rotating groups is also an important factor.


Kolomeisky said the research opens a path for simulating more complex rotor molecules. The chains in ATP-synthase are far too large for a simulation to wrangle, "but as computers get more powerful and our methods improve, we may someday be able to analyze such long molecules," he said.

Tuesday, January 25, 2011

Researchers take molecule's temperature


Researchers take molecule's temperature


You can touch a functioning light bulb and know right away that it's hot. Ouch! But you can't touch a single molecule and get the same feedback.



Rice University researchers say they have the next best thing -- a way to determine the temperature of a molecule or flowing electrons by using Raman spectroscopy combined with an optical antenna.


A new paper from the lab of Douglas Natelson, a Rice professor of physics and astronomy, details a technique that measures the temperature of molecules set between two gold nanowires and heated either by current applied to the wires or laser light. The paper was published this week in the online edition of Nature Nanotechnology.


Natelson, postdoctoral research associate Dan Ward and their colleagues found that while measuring heat at the nanoscale can be much more complicated than taking the temperature of macro objects, it can be done with a level of accuracy that will be of interest to the molecular electronics community or anyone who wants to know how heating and dissipation work at very small scales.


"When you get down to making small electronic devices or tiny junctions, you have to worry about how energy ends up in the form of heat," Natelson said. "In the case of macroscopic objects, like the filament in a light bulb, you can attach a thermocouple -- a thermometer -- and measure it." When light bulbs get hot, they also glow. "If you look at the spectrum of the light coming out, you can figure out how hot it is," he said.


That's an over-simplified version of what Natelson and Ward are doing. One can't see the glow of a molecule. However, the researchers can send in light as a probe and detect the wavelength of the light that molecule is returning when heated. "In Raman scattering, you send in light that interacts with your target. When it comes back, it will either have more energy than you put in, or the same, or less. And we can see that and figure out the effective temperature of whatever is scattering the light."


The new work follows a paper published in September about the lab's creation of nano antennas that concentrate and magnify light up to 1,000 times. That paper focused on the intensity of laser light shot into a gap between the tips of two gold nanowires.


This time, Natelson and Ward spread molecules -- either oligophenylene vinylene or 1-dodecanethiol -- on the surface of a gold nanowire and then broke the wire, leaving a nanoscale gap. When they were fortunate enough to find molecules in the gap -- "the sweet spot" being where the metal wires are closest, Natelson said -- they'd power up and read the resulting spectra.


The experiments were carried out in a vacuum with materials cooled to 80 kelvins (-315 degrees Fahrenheit). The researchers found they could easily detect temperature fluctuations of up to 20 degrees in the molecules.


On the macro level, Natelson said, "You're usually looking at something that's essentially cold. You send in light, it dumps some of the energy into the thing you're looking at and the light comes out with less energy than when you started. With Raman scattering, you can actually see particular molecular vibrational modes."


But the opposite can happen if the atoms are already vibrating with stored energy. "The light can grab some of that and come out with more energy than when it started," he explained.


The effect is most dramatic when current is supplied through the nanowires. "As we crank up the current through this junction, we can watch these different vibrations shaking more and more. We can watch this thing heat up."


Natelson, named by Discover magazine in 2008 as one of the nation's top 20 scientists under age 40, said the experiments show not only how molecules wedged into the nanogap heat up, but also their interaction with the metal wires. "The vibrations show up as sharp peaks in the spectra," he said. "They have very definite energies. Underneath all that, there's this sort of diffuse smear where the light instead is interacting with the electrons in the metal, the actual metal wires."


Natelson said it's extremely hard to get direct information about how heating and dissipation work on nano scales. "In general, you can't do it. There's a lot of modeling, but in terms of experimental things you can actually measure that tell you what's happening, everything is very indirect. This is an exception. This is special. You can see what's happening.


"In our fantasy experiment, we'd say, 'Boy, I wish I could go in with a thermometer,' or, 'I wish I could see each molecule and see how much it's shaking.' And this is effectively a way of doing that. We can really watch these things heat up."