Optical imaging aids cystic fibrosis research

March 27, 2006
March 27, 2006, Atlanta, GA--Researchers are using a multi-functional optical sensing tool to investigate adenosine triposphate (ATP) release and its role in cystic fibrosis.

March 27, 2006, Atlanta, GA--Researchers are using a multi-functional optical sensing tool to investigate adenosine triposphate (ATP) release and its role in cystic fibrosis. This patented technology, developed by a research team led by Christine Kranz at the Georgia Institute of Technology, adds recessed micro- and nano-electrodes to the tip of an atomic force microscope (AFM), creating a single tool that can simultaneously monitor topography along with electrochemical activity at the cell surface.

The new multi-functional imaging technique will advance the study of biological samples, said Boris Mizaikoff, an associate professor at Georgia Tech's School of Chemistry and Biochemistry and director of its Applied Sensors Lab.

"Conventional AFM can image surfaces, but usually provides limited chemical information," he explained. "And though scanning electrochemical microscopy (SECM), another probing technique, provides laterally resolved electrochemical data, it has limited spatial resolution. By combining AFM and SECM functionality into a single scanning probe, our tool provides researchers with a more holistic view of activities at the cell surface."

In the ATP study, sponsored by the National Institutes of Health and done in collaboration with Douglas Eaton at Emory University's School of Physiology, the Georgia Tech team used the multi-scanning biosensors to study ATP release at the surface of live epithelial cells (which cover most glands and organs in the body). ATP, a chemical involved in energy transport, is of interest to medical researchers because elevated levels have been linked with cystic fibrosis, a disease that affects one out of every 2500 people in the United States.

Using epithelial cell cultures from Emory, the Georgia Tech researchers have demonstrated that their multi-functional biosensors work at the live-cell surface during in vitro studies.

"Before you can identify what triggers the ATP release, we must be able to quantitatively measure the released species at the cell surface," Mizaikoff said, noting that many pathological events involve the disruption of chemical communication and molecular signaling between cells, especially in the nervous system, lungs and kidneys.

Improved understanding of cellular communication can lead to new strategies for treating diseases, he added. "Being able to operate sensors in an electrochemical imaging mode at the micro- and nanoscale is an exciting opportunity for complementing optical imaging techniques. There are many clinical research problems that these biosensors can help with."

In addition to Mizaikoff and Kranz, the team includes post-doctoral scholar Jean-Francois Masson and graduate student Justyna Wiedemair.

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