MU Researchers Develop 3D 'Force Microscope' - Could Lead to Faster Drug Therapies
Dec 17, 2013 - 4:13:38 PM
VIDEO: MU Researchers Develop Advanced Three-Dimensional “Force Microscope”
Normally, force microscopes measure the compression of the needle against the specimen by bouncing a single laser off the cantilever, or arm, that holds the microscopic needle in place. As the cantilever moves, it deflects light that is sent back to a highly advanced computer. There, the results are interpreted, giving researchers an idea of how the membrane proteins are interacting with the cell.
Usually, to determine membrane protein structure in detail, specimens must be crystallized, or frozen; therefore, the specimen cannot be studied as it would behave in the primarily liquid environment found in the body.
King and his fellow researcher, Krishna Sigdel, a postdoctoral fellow in the Department of Physics, solved the problem by building their own force microscope that is able to study membrane proteins in conditions similar to those found in the body. Using a traditional one-dimensional force microscope as a guide, the team added an additional laser that measures the second and third dimensions of tip movement, giving researchers "real-time" access to the measurement of peaks and valleys in the membrane protein and dynamic changes in those structures.
"By adding a new laser that is focused from below, we essentially gave the force microscope two additional dimensions," King said. "Using this new laser, we collect the back-scattered light from not only the cantilever holding the needle, but also the tip of the needle that gives additional measurements. This added flexibility allows us to collect information faster and allows our microscope to work in near-native conditions in fluid like those found in the cell, yielding more realistic results."
King suggested that an advantage of three-dimensional force microscopy is that it allows for better interpretation of how a protein's dynamic shape also dictates its function. King said that by studying how the shape of proteins change, researchers can determine how drugs bind and interact with cells. Using membrane protein information, pharmaceutical companies can determine which molecules to pursue.
King's work, "Three-dimensional atomic force microscopy: interaction force vector by direct observation of tip trajectory," was published in NanoLetters, the journal of the American Chemical Society and was funded in part by the National Science Foundation and the Burroughs Wellcome Fund.
The publication was co-written by King, Sigdel and Justin Grayer, who is currently a graduate student in MU's Electrical and Computer Engineering Department.
King's joint appointment in the Department of Biochemistry, which is located in the School of Medicine and the College of Agriculture, Food, and Natural Resources, emphasizes the highly collaborative culture in the area of One Health/One Medicine-one of the four key areas of collaborative strength that distinguish MU collectively known as the Mizzou Advantage. The other three areas are Food for the Future, Sustainable Energy, and Media of the Future.
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