Elegant constrictions in a cellular kill switch

(Press-News.org) The inner workings of a "self-destruct switch" present on human cells that can be activated during an immune response have been revealed. In unprecedented detail, KAUST scientists with collaborators in China report the 3D atomic structure of the human PANX1 protein, which may help underpin new therapies that target the immune system.

When cells become infected with a pathogen, the body's immune system works to destroy the infected cells before they become a threat to surrounding tissues. This form of cell death, during which a cell releases potent danger signals to recruit immune cells, is known as pyroptosis.

The protein PANX1, a channel pore that dots a cell's outer membrane, has been implicated in pyroptosis because it allows the passage of ions and molecules out of the cell, which helps mark it for destruction. But how it carries out this function, or "flicks the switch" on cell death, has been unclear.

"We wanted to know the gating mechanisms of PANX1 by resolving the previously unrevealed protein ends -- the C- and N-termini -- to understand their importance in pyroptosis," says study co-first author Baolei Yuan, a Ph.D. student in Mo Li's lab.

Li's collaborators, led by Maojun Yang at Tsinghua University, first isolated the protein and revealed the 3D structure using data collected on KAUST's state-of-the art Titan Krios cryo-transmission electron microscope and a similar instrument at Tsinghua University.

Through this, the researchers visualized a number of amino acids within the protein that "pinch" the pore to control the passage of molecules across the cell membrane. Using cultured cells, Li's team confirmed the indispensable role these amino acids and PANX1 play in pyroptosis.

But the molecular details of how ions and molecules cross the PANX1 pore only became clear when the researchers teamed up with Xin Gao, whose group was able to simulate the molecular dynamics.

"I was surprised by the intricate and beautifully arranged constrictions in the permeation path of the PANX1 channel," says Yuan.

Together, the cryo-EM and molecular dynamics data revealed that the N- and C-termini stretch deeply into the pore to form barriers under normal conditions to keep ions and small components inside the cells. But once stimulated, the two termini are either modified or cleaved to make the channel more permeable, releasing molecules that help destroy the cell.

"These findings give us a much better understanding of the mechanism that controls pyroptosis," says Li. "PANX1 has been associated with diverse and numerous pathophysiological conditions related to the immune system. Our study provides a high-quality reference for potential drug targets."

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