Scientists decipher the structure, key features of a critical immune-surveillance protein in humans

phys.org | 7/12/2018 | Staff
Fubu_chik (Posted by) Level 3


The human body is built for survival. Each one of its cells is closely guarded by a set of immune proteins armed with nearly foolproof radars that detect foreign or damaged DNA.

One of the cells' most critical sentinels is a "first responder" protein known as cGAS, which senses the presence of foreign and cancerous DNA and initiates a signaling cascade that triggers the body's defenses.

Discovery - CGAS - Firestorm - Inquiry - Research

The 2012 discovery of cGAS ignited a firestorm of scientific inquiry, resulting in more than 500 research publications, but the structure and key features of the human form of the protein continued to elude scientists.

Now, scientists at Harvard Medical School and Dana-Farber Cancer Institute have, for the first time, identified the structural and functional differences in human cGAS that set it apart from cGAS in other mammals and underlie its unique function in people.

Report - Team - Work - July - Cell

A report on the team's work, published July 12 in Cell, outlines the protein's structural features that explain why and how human cGAS senses certain types of DNA, while ignoring others.

"The structure and mechanism of action of human cGAS have been critical missing pieces in immunology and cancer biology," said senior investigator Philip Kranzusch, assistant professor of microbiology and immunobiology at Harvard Medical School and Dana-Farber Cancer Institute. "Our findings detailing the molecular makeup and function of human cGAS close this critical gap in our knowledge."

Findings - Design - Drugs - Features - Protein—an

Importantly, the findings can inform the design of small-molecule drugs tailored to the unique structural features of the human protein—an advance that promises to boost the precision cGAS-modulating drugs that are currently in development as cancer therapies.

"Several promising experimental immune therapies currently in development are derived from the structure of mouse cGAS, which harbors key structural differences with human cGAS," Kranzusch said. "Our discovery should help refine these experimental therapies and spark the design of new ones. It...
(Excerpt) Read more at: phys.org
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