Scientists determine the atomic-level structure of a zinc-transporter protein

Scientists at the U.S. Department of Energy's (DOE) Brookhaven National Laboratory have determined the atomic-level structure of a zinc-transporter protein, a molecular machine that regulates levels of this crucial trace metal micronutrient inside cells. As described in a paper just published in Nature Communications, the structure reveals how the cellular membrane protein shifts its shape to move zinc from the environment into a cell, and temporarily blocks this action automatically when zinc levels inside the cell get too high.

"Zinc is important for many biological activities, but too much can be a problem," said Qun Liu, the Brookhaven Lab biophysicist who led the project. "During evolution, different organisms have evolved in many ways to regulate zinc. But no one has shown that a transporter that controls the uptake of zinc from the environment can regulate its own activity. Our study is the first to show a zinc transporter with such a built-in sensor."

The research was conducted as part of Brookhaven Lab's Quantitative Plant Sciences Initiative (QPSI). Using a bacterial version of a zinc transporter that shares essential features with zinc transporters in plants, the scientists gained key insights into how these proteins work.

"This research is part of our effort to understand how micronutrients like zinc are taken up by plants so we can understand how to design plants that are better able to grow on marginal land for the production of bioenergy," said Brookhaven Lab Biology Department Chair John Shanklin, a co-author on the paper.

The research could also suggest ways to engineer food crops with increased zinc content to improve their nutritional value, the scientists noted.

Cryo-EM plus computation

To solve the protein structure, the Brookhaven team used cryo-electron microscopy (cryo-EM) at the Laboratory for BioMolecular Structure (LBMS). With this technique, scientists can sample many different conformations of a protein instead of a single, crystallized form. That's important because, in nature, proteins are dynamic, not static; pieces of them move around.

Cryo-EM does not require proteins to form crystals, so we can actually capture dynamic steps that may not feasible using x-ray crystallography, another technique for studying protein structures. In essence, with cryo-EM, we can capture more frames of the 'movie' to get a structure that is very helpful in understanding a protein's biological function."

Qun Liu, Biophysicist, Brookhaven Lab

To sort through the many variations in structure, the scientists need powerful computational tools. These include artificial intelligence approaches that use machine learning, some of which Liu has developed. Using these algorithms, the scientists can semi-automatically select and sort through millions of cryo-EM images to find groups of structures with similarities. The method allows them to achieve the highest feasible resolution, and thus to reveal atomic-scale details of the structure.

For this study, this cryo-EM approach revealed key features of one stage of a ZIP (Zrt-/Irt-like protein) zinc transporter that reveals how it regulates its own zinc-uptake activity depending on how much zinc is already in the cell.

"Our new data made us revise the previous views as to how this protein works," Liu said.

Tilt to enter, sense to stop

An earlier report based on x-ray crystallography and coevolutional analyses suggested that the transporter may function as a sort of "elevator" to transport zinc. The new research shows how interactions with zinc on either side of the cellular membrane trigger the movement of parts of the protein to bring zinc into the cell-;and, crucially, block its entry when the levels inside get too high.

"Our key structure shows that when the zinc level inside the cell rises to a certain level-;beyond what's required to meet the cell's demands-;the excess zinc binds to a loop on the inside of the membrane," Liu said. "Then, as this flexible loop reorients, it folds back on itself, and binds in a manner that blocks zinc from entering the cell."

"It's almost like the plug going into a bathtub drain and blocking it," Shanklin added.

The scientists also worked out how other parts of the protein move to allow zinc to enter.

When zinc levels inside the cell are low, zinc falls off the loop portion and the plug pops back out of the transporter. Zinc from the environment can move into the transporter. Inside the transporter, the zinc causes part of the protein machine to move up and tilt, closing the exit to the external environment. Once the zinc moves into the cell, the machine will reset itself to work again.

"Our cryo-EM structure is the first to show how this loop domain of the protein modulates the transporter's activity by feedback depending on the level of zinc," Liu said.

It's also the first structure to show that this zinc transporter is an arrangement of two identical proteins-;known as a dimer. "It requires two molecules to do the work," Liu said.

The scientists' think that having two molecules acting in the form of a dimer may be related to its function or stability-;which they'll explore with future computational simulations of how the molecules work together.

"This research could enable new ways of engineering zinc transporters in microbes and plants to optimize their growth in conditions where zinc is too low or too high, potentially on marginal lands for the production of bioenergy and bioproducts," Liu said.

This research was funded by the DOE Office of Science, Office of Biological and Environmental Research (BER) through QPSI, with protein expression, purification, and sample preparation supported by the Office of Basic Energy Sciences (BES). LBMS operations are supported by BER.

Journal reference:

Pang, C., et al. (2023). Structural mechanism of intracellular autoregulation of zinc uptake in ZIP transporters. Nature Communications.


The opinions expressed here are the views of the writer and do not necessarily reflect the views and opinions of News Medical.
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