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Home > Press > First reported video of cellís recognition of danger through its protein response made by Sandia and UNM researchers

Total internal reflection fluorescence (TIRF) microscope time-lapse image of quantum-dot labeled proteins fluorescing on the surface of a cell membrane.
Total internal reflection fluorescence (TIRF) microscope time-lapse image of quantum-dot labeled proteins fluorescing on the surface of a cell membrane.

Abstract:
"Like using cameras to watch individual bank robbers move around as a holdup progressed," says scientist

First reported video of cellís recognition of danger through its protein response made by Sandia and UNM researchers

ALBUQUERQUE, NM | Posted on August 14th, 2008

Cells are expected to respond defensively when an antigen lands on a cell membrane and prepares to cause mischief.

But to activate a response, a cell must become aware of the presence of the intruder on its membrane, just as a human first must become aware of a mosquito on a forearm in order to slap it.

In joint experimental work, physicists at Sandia National Laboratories and biologists at the University of New Mexico's Cancer Research and Treatment Center have combined unusual techniques to make real-time movies that show exactly how a 50-nanometer-thick membrane notifies the cell it encloses that a hostile alien presence ó an antigen ó has made a landing.

And also why notification may not take place.

"We were able to characterize the motion of the receptor proteins in the membrane in real time as they respond to the antigen," says lead Sandia researcher Alan Burns. "Perhaps more importantly, we learned the cell membrane is really complicated and highly structured, rather than fluid and unstructured, as is the prevailing notion."

The membrane structures, which resemble holding corrals, says Burns, do move around in the membrane. But they restrict the motion of proteins. The response of the cell requires that the antigen receptor proteins cluster with other proteins to commence the cellular signaling network.

"The proteins are like Paul Revere giving a warning," says Burns. "When proteins bind antigens, they begin to cluster. This causes other proteins to thrash around. That sends a message from the membrane to the cell nucleus that something's wrong.

"But if there are places on the membrane that are walled off and an antigen lands there, the cell may not be notified there's a problem. No protein, no warning."

UNM researchers already knew that incoming antigens were detected by proteins present in the lipid matrix of the cell membrane. But how exactly to determine the process?

Burns, working with his former Sandia postdoctoral student Keith Lidke (now a UNM professor), modified a special microscope called a total internal reflection fluorescence (TIRF) microscope, whose laser-light output is completely contained within the microscope coverslip. This resembles the way optical fibers transport light, except that the TIRF does not ever release any light. But though the light is contained, making its use seem at first an exercise in futility because it penetrates nothing external, it generates a tiny electrical exploratory field that extends about 100 nm into the cell, which lies supported by the coverslip.

"When a cell settles on a piece of bare thin glass," says Burns, "the membrane of the cell by definition is snuggled up against the glass and available to the radiation field."

Enter the UNM biology team. Led by professor Diane Lidke, the team was able to attach quantum dots of 8 nm and 11 nm respectively to two different types of antigen receptor proteins in the membrane.

Quantum dots emit light when stimulated by an electrical field. The color fluoresced is determined by the size of the dot. So one protein, when stimulated by the laser's electrical field, emitted orange light. The other emitted red. That way researchers could keep track of the motion of single, individual proteins and see how they interacted; moreover, it allowed them to observe barriers to the motion.

Sensitive CCD cameras picked up and videotaped the motion of the lit-up proteins as they reacted to the introduction of antigens to the membrane.

"It was like using cameras to watch individual bank robbers move around as a holdup progressed," says Burns.

The work is of interest to Sandia, a national defense lab interested in determining the human response to bioinfectious diseases, and to UNM's bioscience program.

Other authors on the paper were graduate student Nicholas Andrews and pathology professors Bridget Wilson and Janet Oliver, all with UNM's Cancer Research and Treatment Center.

The Sandia work was funded by its Laboratory Directed Research and Development office. The National Institutes of Health funded the UNM portion.

The work was published online the week of July 20 in the journal Nature Cell Biology.

####

About Sandia National Laboratories
Sandia is a multiprogram laboratory operated by Sandia Corporation, a Lockheed Martin company, for the U.S. Department of Energyís National Nuclear Security Administration. With main facilities in Albuquerque, N.M., and Livermore, Calif., Sandia has major R&D responsibilities in national security, energy and environmental technologies, and economic competitiveness.

For more information, please click here

Contacts:
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(505) 845-7078

Copyright © Sandia National Laboratories

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Video 1 - The proteins move freely on the cell surface until the allergen binds, linking the proteins together. This causes them to stop moving. and also to start associating with other proteins inside the cell. This causes the cell to release histamine.

Video 2 - QD-IgE (red) proteins are moving on the cell surface, avoiding actin structures (green). Actin is a protein that makes up the "skeleton" of the cell.

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