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Monday, January 13th, 2014

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    8:00p
    Weighing particles at the attogram scale
    MIT engineers have devised a way to measure the mass of particles with a resolution better than an attogram — one millionth of a trillionth of a gram. Weighing these tiny particles, including both synthetic nanoparticles and biological components of cells, could help researchers better understand their composition and function.

    The system builds on a technology previously developed by Scott Manalis, an MIT professor of biological and mechanical engineering, to weigh larger particles, such as cells. This system, known as a suspended microchannel resonator (SMR), measures the particles’ mass as they flow through a narrow channel.

    By shrinking the size of the entire system, the researchers were able to boost its resolution to 0.85 attograms —more than a 30-fold improvement over the previous generation of the device.

    “Now we can weigh small viruses, extracellular vesicles, and most of the engineered nanoparticles that are being used for nanomedicine,” says Selim Olcum, a postdoc in Manalis’ lab and one of the lead authors of a paper describing the system in this week’s issue of the Proceedings of the National Academy of Sciences.

    Graduate student Nathan Cermak is also a lead author of the paper, and Manalis, a member of MIT’s Koch Institute for Integrative Cancer Research, is the paper’s senior author. Researchers from the labs of MIT professors and Koch Institute members Angela Belcher and Sangeeta Bhatia also contributed to the study.

    A small sensor for small particles

    Manalis first developed the SMR system in 2007 to measure the mass of living cells, as well as particles as small as a femtogram (one quadrillionth of a gram, or 1,000 attograms). Since then, his lab has used the device to track cell growth over time, measure cell density, and measure other physical properties, such as stiffness.

    The original mass sensor consists of a fluid-filled microchannel etched in a tiny silicon cantilever that vibrates inside a vacuum cavity. As cells or particles flow through the channel, one at a time, their mass slightly alters the cantilever’s vibration frequency. The mass of the particle can be calculated from that change in frequency.

    To make the device sensitive to smaller masses, the researchers had to shrink the size of the cantilever, which behaves much like a diving board, Olcum says. When a diver bounces at the end of a diving board, it vibrates with a very large amplitude and low frequency. When the diver plunges into the water, the board begins to vibrate much faster because the total mass of the board has dropped considerably.

    To measure smaller masses, a smaller “diving board” is required. “If you’re measuring nanoparticles with a large cantilever, it’s like having a huge diving board with a tiny fly on it. When the fly jumps off, you don’t notice any difference. That’s why we had to make very tiny diving boards,” Olcum says.

    In a previous study, researchers in Manalis’ lab built a 50-micron cantilever — about one-tenth the size of the cantilever used for measuring cells. That system, known as a suspended nanochannel resonator (SNR), was able to weigh particles as light as 77 attograms at a rate of a particle or two per second.

    The cantilever in the new version of the SNR device is 22.5 microns long, and the channel that runs across it is 1 micron wide and 400 nanometers deep. This miniaturization makes the system more sensitive because it increases the cantilever’s vibration frequency. At higher frequencies, the cantilever is more responsive to smaller changes in mass.

    The researchers got another boost in resolution by switching the source for the cantilever’s vibration from an electrostatic to a piezoelectric excitation, which produces a larger amplitude and, in turn, decreases the impact of spurious vibrations that interfere with the signal they are trying to measure.

    With this system, the researchers can measure nearly 30,000 particles in a little more than 90 minutes. “In the span of a second, we’ve got four or five particles going through, and we could potentially increase the concentration and have particles going through faster,” Cermak says.

    Particle analysis

    To demonstrate the device’s usefulness in analyzing engineered nanoparticles, the MIT team weighed nanoparticles made of DNA bound to tiny gold spheres, which allowed them to determine how many gold spheres were bound to each DNA-origami scaffold. That information can be used to assess yield, which is important for developing precise nanostructures, such as scaffolds for nanodevices.

    The researchers also tested the SNR system on biological nanoparticles called exosomes — vesicles that carry proteins, RNA, or other molecules secreted by cells — which are believed to play a role in signaling between distant locations in the body.

    They found that exosomes secreted by liver cells and fibroblasts (cells that make up connective tissue) had different profiles of mass distribution, suggesting that it may be possible to distinguish vesicles that originate from different cells and may have different biological functions.

    The researchers are now investigating using the SNR device to detect exosomes in the blood of patients with glioblastoma (GBM), a type of brain cancer. This type of tumor secretes large quantities of exosomes, and tracking changes in their concentration could help doctors monitor patients as they are treated.

    Glioblastoma exosomes can now be detected by mixing blood samples with magnetic nanoparticles coated with antibodies that bind to markers found on vesicle surfaces, but the SNR could provide a simpler test.

    “We’re particularly excited about using the high precision of the SNR to quantify microvesicles in the blood of GBM patients. Although affinity-based approaches do exist for isolating subsets of microvesicles, the SNR could potentially provide a label-free means of enumerating microvesicles that is independent of their surface expression,” Manalis says.

    The research was funded by the U.S. Army Research Office through the Institute for Collaborative Biotechnologies, the Center for Integration of Medicine and Innovative Technology, the National Science Foundation, and the National Cancer Institute.
    8:00p
    How the immune system fights off malaria
    The parasites that cause malaria are exquisitely adapted to the various hosts they infect — so studying the disease in mice doesn’t necessarily reveal information that could lead to drugs effective against human disease.

    Now, a team led by MIT researchers has developed a strain of mice that mimics many of the features of the human immune system and can be infected with the most common human form of the malaria parasite, known as Plasmodium falciparum. Using this strain, the researchers have already identified a key host defense mechanism, and they believe it should lead to many more useful discoveries.

    “Human malaria studies have been hampered by a lack of animal models,” says Jianzhu Chen, the Ivan R. Cottrell Professor of Immunology, a member of MIT’s Koch Institute for Integrative Cancer Research, and the lead principal investigator of the Infectious Disease Interdisciplinary Research Group at the Singapore-MIT Alliance for Research and Technology (SMART). “This paves the way to start dissecting how the host human immune system interacts with the pathogen.”

    Chen is one of the senior authors of a paper describing the findings in this week’s Proceedings of the National Academy of Sciences, along with Ming Dao, a principal research scientist in MIT’s Department of Materials Science and Engineering (DMSE); Subra Suresh, president of Carnegie Mellon University (and a former MIT dean of engineering and the Vannevar Bush Professor Emeritus of Engineering); and Peter Preiser, a professor at Nanyang Technology University in Singapore.

    Plasmodium falciparum, a parasite carried by mosquitoes, usually infects the liver and red blood cells of its victims. Scientists hoping to study malaria in mice have previously generated mice with human red blood cells — but these mice also have compromised immune systems, so they can’t be used to study the immune response to malaria infection.

    The humanized mouse project described in the new PNAS study grew out of an interdisciplinary program Suresh initiated in 2003 involving researchers from MIT, several institutions in Singapore, and the Institut Pasteur in France to study the mechanobiology of human red blood cells invaded by malaria parasites and its consequences for the pathogenesis of malaria. In 2007, Chen, Suresh, Dao, and Preiser established a collaboration, through SMART, to develop a humanized mouse model for malaria.

    Over the past several years, Chen and colleagues have developed strains of mice that have the human cells necessary for a comprehensive immune response. To generate these cells, the researchers deliver human hematopoietic stem cells, along with cytokines that help them mature into B and T cells, natural killer (NK) cells, and macrophages — all critical components of the immune system. These mice have already proven useful to study other diseases, such as dengue fever.

    To adapt the mice for the study of malaria, the researchers injected them with human red blood cells every day for a week, at which point 25 percent of their red blood cells were human — enough for the malaria parasite to cause an infection.

    Natural defense

    In the new PNAS paper, the researchers investigated the role of NK cells and macrophages during the first two days of malaria infection. They found that eliminating macrophages had very little impact on the immune response during those early stages. However, in mice lacking NK cells, parasite levels went up sevenfold, suggesting that NK cells are critical to controlling infection early on.

    To further investigate the role of NK cells, the researchers placed human NK cells in a sample of infected and uninfected red blood cells. The NK cells randomly interacted with both types of cells, but they latched onto infected cells much longer, eventually killing them.

    This indicates that NK cells may provide an important immune defense against malaria, says Lewis Lanier, a professor of microbiology and immunology at the University of California at San Francisco. “These findings will prompt future studies in infected humans and suggest that augmenting NK cell function might provide a new therapeutic strategy for malaria,” says Lanier, who was not part of the research team.

    The researchers also identified a cell adhesion protein called LFA-1 that helps NK cells bind to red blood cells. They are now studying this process in more detail and trying to figure out what other molecules, including those produced by the malaria parasite, might be involved.

    Chen and colleagues also hope to use these mice to study experimental malaria vaccines or drugs. And in another future study, they plan to inject the mice with human red blood cells from people with sickle cell anemia to investigate how the sickle-shaped red blood cells help people survive malaria infection.

    The research was funded by the National Research Foundation Singapore through SMART’s Interdisciplinary Research Group in Infectious Disease.

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