Researchers reveal crucial immune fighter role of the STING protein

Researchers at Weill Cornell Medical College have unlocked the structure of a key protein that, when sensing certain viruses and bacteria, triggers the body's immediate immune response.

In the journal Molecular Cell, scientists describe the double wing-like crystal structure of this key protein, known as STING, which is a soldier on the front-line of the body's defense against . Researchers also show STING in action, displaying evidence of a -- an action that launches the body's .

"Activation of STING is crucial to the ability of the human body to pick out bits of molecules secreted by pathogens, including many different , and alert the human body that they are there. By solving the structure of this protein, we now know how they do this crucial task," says the study's lead author, Dr. Qian Yin, a postdoctoral associate in the laboratory of Dr. Hao Wu, professor of Biochemistry at Weill Cornell Medical College.

"The STING structure provides a remarkable example of the pathogen-host interactions in which a unique microbial molecule directly engages the system," says Dr. Wu, the study's senior investigator and director of the Lab of Cell Signaling at Weill Cornell.

While the findings have no immediate clinical significance, they might be useful in helping to make vaccines against pathogens more effective. "Based on the structure we have of STING interacting with molecules secreted from bacteria, we may be able to design new molecules that induce a stronger, more persistent immune response," says Dr. Yin.

STING's wings and tail respond to invaders

All plant and animal life use an innate immune response to recognize and respond to an assault by pathogens. This primitive response is immediate, but not long-lasting or protective; the secondary, sets up the long-term defense.

Previously, scientists thought the innate response was generic, but recently, investigators uncovered proteins expressed by cells of the that identify specific molecular patterns linked to microbial pathogens. STING was recently identified as a member of a family of proteins that is involved in this pattern recognition task. It is specifically tasked at finding viruses that have double-stranded DNA genomes, and with locating bacteria.

While STING does not confront viruses or viral molecules directly, with bacteria, STING is on the lookout for small molecules that bacteria use to communicate within their cellular bodies. These molecules are cyclic-di-GMP, produced by most bacteria, and cyclic-di-AMP, used by bacteria that grow inside the cells of a host.

However STING is activated, the end result is the same, Dr. Yin says. STING induces a response from interferon, which activates other immune cells that kill the invading parasites.

The of STING developed by the research team explains the overall structure of the protein. The second structure of STING, bound to cyclic-di-GMP, explains how the protein can recognize and pick up both cyclic-di-GMP and cyclic-di-AMP. This and other published data suggests how STING activates an .

Dr. Yin describes STING's structure as two wings, which form the bottom and sides that hold cyclic-di-GMP. "It is like two people holding out their left or right hands, wrists joining and palms facing each other, and holding something in their palms."

"The amazing thing is STING only binds to cyclic-di-GMP and, to a lesser degree, cyclic-di-AMP, leaving all other nucleotides in the quite safe -- meaning it is not picking up natural human molecules," she says. "To use the hands analogy again, only cyclic-di-GMP and cyclic-di-AMP can fit into the space between the two hands. Other nucleotides are too small and they will slip."

The researchers also propose that once STING's wings picks up cyclic-di-GMP, the molecule frees up the tail of STING's protein? which then engages with other proteins.

"We believe this movement of the tail section of the protein is the switch that turns on the interferon response," says Dr. Yin.

"This work has uncovered a number of unexpected insights into how STING works," says Dr. Wu. "By binding tightly only to tiny molecules produced by bacteria, which then turns on the interferon switch, it prevents the immune system from attacking the body's own cells."

Related Stories

A molecular brake for the bacterial flagellar nano-motor

Mar 19, 2010

Researchers at the University of Basel, Switzerland, have discovered that Escherichia coli bacteria harness a sophisticated chemosensory and signal transduction machinery that allows them to accurately control ...

Recommended for you

The impact of bacteria in our guts

8 hours ago

The word metabolism gets tossed around a lot, but it means much more than whether you can go back to the buffet for seconds without worrying about your waistline. In fact, metabolism is the set of biochemical ...

Stem cell therapies hold promise, but obstacles remain

8 hours ago

(Medical Xpress)—In an article appearing online today in the journal Science, a group of researchers, including University of Rochester neurologist Steve Goldman, M.D., Ph.D., review the potential and ch ...

New hope in fight against muscular dystrophy

9 hours ago

Research at Stockholm's KTH Royal Institute of Technology offers hope to those who suffer from Duchenne muscular dystrophy, an incurable, debilitating disease that cuts young lives short.

Biologists reprogram skin cells to mimic rare disease

Aug 21, 2014

Johns Hopkins stem cell biologists have found a way to reprogram a patient's skin cells into cells that mimic and display many biological features of a rare genetic disorder called familial dysautonomia. ...

User comments