Unlocking the secrets of how cells communicate offers insights into treating diseases

December 12, 2018, Portland State University
Unlocking the secrets of how cells communicate offers insights into treating diseases
2-D images, left, and the 3D structure, right, of the gap junction communication channel from the eye lens, resolved to near-atomic resolution by the Reichow Lab using cryo-electron microscopy Credit: Reichow Lab | Portland State University

Portland State University researchers have made a significant breakthrough by developing the 3-D structure of proteins from inside the eye lens that control how cells communicate with each other, which could open the door to treating diseases such as cataracts, stroke and cancer.

The PSU research team, led by chemistry professor Steve Reichow, used a multimillion-dollar microscope and a developed by three Nobel Prize-winning biophysicists called (Cryo-EM) to view membrane channels—or transportation tunnels in cell walls—at the atomic level. This allowed Reichow's team, whose research is supported by the National Institutes of Health, to create a 3-D image of the membrane to better understand the processes involved in cell-to-cell communication.

Portland State researchers used Cryo-EM—a microscope technique that freezes biomolecules in mid-movement and takes ultra-high-resolution images—and computer modeling to see the 3-D structure of gap junction proteins that had been isolated from eye lenses. Gap junctions are tiny channels that allow neighboring cells to communicate with one another and are found in many places throughout the body.

Their findings—published Dec. 12 in the scientific journal Nature - showed for the first time how selectively pass or block chemical information. Until now, it was not known how these channels would allow certain messages to pass between cells while specifically blocking others.

Steve Reichow, an assistant professor of chemistry at Portland State University, talks about how his lab uses cryo-electron microscopy to view membrane protein channels at the atomic level, and what that means for medical research. Credit: Portland State University

Reichow said the detailed images may open the door to understanding, and potentially treating, different types of diseases that are associated with the loss of function in cellular communication involving gap junctions such as cataracts, cardiac arrhythmia, stroke and certain cancers.

"Currently there's no drug on the market today that can specifically block or activate gap junction proteins," Reichow said. "But our discovery may one day pave the way for development of pharmaceuticals that can control heart disease or other diseases that are associated with the malfunctions or mis-regulations of these protein channels."

Members of Portland State University's Reichow Lab and co-authors of the study, graduate student Bassam Haddad (center, holding an eye lens), graduate student Janette Myers, assistant chemistry professor Steve Reichow, and senior research assistant Susan O'Neill Credit: Peter Simon | Portland State University

Now that the Reichow Lab has established a method for characterizing the proteins, they are trying to understand the nuances of how the body uses gap junctions differently across tissues and organs.

Explore further: 'Scaffolding' method allows biochemists to see proteins in remarkable detail

More information: Janette B. Myers et al, Structure of native lens connexin 46/50 intercellular channels by cryo-EM, Nature (2018). DOI: 10.1038/s41586-018-0786-7

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