"It's really giving us a molecular-level picture of what's going on," said Matthew Lang, an assistant professor of biological and mechanical engineering and senior author of a paper on the work appearing in the June 30 advanced online issue of the Proceedings of the National Academy of Sciences.
Last fall, Lang and others demonstrated that light beams could be used to pick up and move individual cells around the surface of a microchip.
Now they have applied the optical tweezers to measuring protein microarchitectures, allowing them to study the forces that give cells their structure and the ability to move.
The researchers focused on proteins that bind to actin filaments, an important component of the cytoskeleton. Depending on the arrangement and interaction of actin filaments, they can provide structural support, help the cell crawl across a surface or sustain a load (in muscle cells).
"We're trying to understand how nature engineered these molecular linkages to use in different ways," said Lang.
Actin filaments are most commonly found either bonded or crosslinked by a much smaller actin binding protein.
The researchers studied the interactions between the proteins by pinning one actin filament to a surface and controlling the motion of the second one with a beam of light. As the researchers tug on a bead attached to the second filament, the bond mediated by the actin-binding protein eventually breaks.
With this technique, the researchers can get a precise measurement of the force holding the proteins together, which is on the order of piconewtons (10^-12 newtons).
The same technique could be used to investigate many of the other hundreds of protein interactions that occur in the cytoskeleton, said Lang.
Source: Massachusetts Institute of Technology
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