Columbia University Medical Center

Electron Microscope Images Reveal How Cells Absorb a Vital Mineral

First glimpse of a calcium membrane pore in action identifies a potential target for treating cancer

TRPV6 channel in closed and open states. (Credit: Sobolevsky lab)

New York, NY (Dec. 20, 2017)—Columbia University Medical Center (CUMC) researchers have obtained the first detailed snapshots of the structure of a membrane pore that enables epithelial cells to absorb calcium. The findings could accelerate the development of drugs to correct abnormalities in calcium uptake, which have been linked to cancers of the breast, endometrium, prostate, and colon.

The study was published today in the online edition of Nature.

Although most of the body’s calcium is stored as a mineral in bones, a carefully controlled amount of this chemical element is transported into the cell, in its ionic form, where it plays a vital role in governing cellular functions. Cells regulate calcium uptake through special pores, or channels, that open and close as needed. TRPV6 is a protein channel that is located in the membranes of epithelial cells, which line the walls of the intestine, and contributes to the uptake of dietary calcium. Aberrations in TRPV6 channels may contribute to the development of cancer by disrupting the control of cell proliferation and cell death.

The researchers used advanced cryo-electron microscopy to image TRPV6. Cryo-electron microscopy—an imaging technique that combines thousands of individual images of frozen molecules into finely detailed three-dimensional representations—was pioneered by Joachim Frank, PhD, a structural biologist at CUMC who was awarded the 2017 Nobel Prize in Chemistry for this work.

By comparing the channel structures, in both the open and closed states, the researchers were able to determine that the core portion of the channel—four tightly aligned helical protein segments—do a subtle twist, allowing TRPV6 to open.

“We discovered that the calcium channel opens in response to changes in the middle portion of each core helix, causing the protein segments to bend and rotate outward to create an opening just wide enough to allow a calcium ion to pass through,” said study leader Alexander I. Sobolevsky, PhD, associate professor of biochemistry & molecular biophysics at Columbia. “If one were able to look straight down the channel, it would look like the opening of the iris of an eye.”

The channel can switch between open and closed states extremely quickly, as needed to supply the cell with calcium.

“Our findings will help us better understand how changes in TRPV6 channels contribute to human diseases such as cancer and provide a template for the design of drugs that correct these abnormalities,” said Dr. Sobolevsky.

The TRPV6 calcium channel opens in response to changes in the middle portion (teal) of each core helix, causing the protein segments to bend and rotate outward to create an opening just wide enough to allow a calcium ion to pass through. (Credit: Sobolevsky lab).

About:
The study is titled “Opening of the human epithelial calcium channel TRPV6.” The other contributors (all at CUMC) are Luke L. McGoldrick, Appu K. Singh, Kei Saotome, Maria V. Yelshanskaya, Edward C. Twomey, and Robert A. Grassucci.

The study was supported by grants from the National Institutes of Health (T32 GM008224, F31 NS093838, R01 CA206573, R01 NS083660, and GM103310), the Simons Foundation, and NYSTAR and by Amgen Young Investigator and Irma T. Hirschl Career Scientist awards.

The authors declare no financial or other conflicts of interest.

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