Electron microscope images reveal how cells absorb a vital mineral

The study was published 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 contribute 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 in the biochemistry department at CUMC, who was awarded the Nobel Prize in Chemistry in October 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 and molecular biophysics at CUMC. "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.