Researchers have discovered a ‘guard mechanism’ in the protein GBP1 that regulates its ability to attack microbes in infected cells. This discovery explores the interaction between GBP1 and PIM1 and has implications for potential treatments against diseases like Toxoplasma, Chlamydia, Tuberculosis, and cancer. The control mechanism, likened to a “lock and key” system, could offer innovative therapeutic interventions.
The attack protein guard mechanism can be used to kill pathogens like Toxoplasma and cancer cells.
Researchers have identified a ‘guard mechanism’ for GBP1, a protein known for targeting microbes within infected cells. This groundbreaking discovery could pave the way for innovative treatments against diseases such as Toxoplasma, Chlamydia, Tuberculosis, and even cancer.
A recent study spearheaded by the University of Birmingham and published in the journal Science has discovered the lock and key mechanism that controls the attack protein GPB1. GBP1 is activated during inflammation and has the potential to attack membranes within cells and destroy them.
Lock and Key Mechanism
This research has uncovered that GBP1’s activity is managed through phosphorylation – a procedure in which a phosphate group is added to a protein by enzymes called protein kinases. The kinase targeting GBP1 is called PIM1 and can also become activated during inflammation. Phosphorylated GBP1 in turn is bound to a scaffold protein, which keeps uninfected bystander cells safe from uncontrolled GBP1 membrane attack and cell death.
The newly discovered mechanism prevents GPB1 from attacking cell membranes indiscriminately, creating a guard mechanism that is sensitive to disruption by the actions of pathogens inside the cells. The new discovery was made by Daniel Fisch, a former Ph.D. student in the Frickel lab working on the study.
Dr Daniel Fisch said: “This was a fantastic project to work on for the past six years and involved many research groups from all over the world. None of this would have been possible without help from our colleagues and friends at The Francis Crick Institute in London, EMBL in Grenoble (France), ETH Zurich (Switzerland), and Osaka University (Japan).”
Implications and Future Research
Dr Eva Frickel, Senior Wellcome Trust Fellow at the University of Birmingham, who led the study explained: “This discovery is significant for several reasons. Firstly, guard mechanisms such as the one that controls GBP1 were known to exist in plant biology, but less so in mammals. Think of it as a lock and key system. GPB1 wants to go out and attack cellular membranes, but PIM1 is the key meaning GPB1 is locked safely away.“
“The second reason is that this discovery could have multiple therapeutic applications. Now we know how GBP1 is controlled, we can explore ways to switch this function on and off at will, using it to kill pathogens.”
Dr Frickel and her team conducted this initial research on Toxoplasma gondii, a single-celled parasite that is common in cats. Whilst Toxoplasma infections in Europe and Western countries are unlikely to cause serious illness, in South American countries it can cause reoccurring eye infections and blindness and is particularly dangerous for pregnant women.
The researchers found that Toxoplasma blocks inflammatory signaling within cells, preventing PIM1 from being produced, meaning that the “lock and key” system disappears, liberating GBP1 to attack the parasite. Switching PIM1 ‘off’ with an inhibitor or by manipulating the cell’s genome also resulted in GPB1 attacking Toxoplasma and removing the infected cells.
Dr Frickel continued: “This mechanism could also work on other pathogens, such as Chlamydia, Mycobacterium tuberculosis, and Staphylococcus all major disease-causing pathogens that are increasingly becoming more resistant to antibiotics. By controlling the guard mechanism, we could use the attack protein to eliminate the pathogens in the body. We have already begun looking at this opportunity to see if we are able to replicate what we saw in our Toxoplasma experiments. We are also incredibly excited about how this could be used to kill cancer cells.”
PIM1 is a key molecule in the survival of cancer cells, while GPB1 is activated by the inflammatory effect of cancer. The researchers think that by blocking the interaction between PIM1 and GPB1 they could specifically eliminate cancer cells.
Dr Frickel said: “The implication for cancer treatment is huge. We think this guard mechanism is active in cancer cells, so the next step is to explore this and see if we can block the guard and selectively eliminate cancer cells. There is an inhibitor on the market that we used to disrupt PIM1 and GPB1 interaction. So, if this works, you could use this drug to unlock GPB1 and attack the cancer cells. There is still a very long way to go, but the discovery of the PIM1 guard mechanism could be a massive first step in finding new ways to treat cancer and increasingly antibiotic-resistant pathogens.”
Reference: “PIM1 controls GBP1 activity to limit self-damage and to guard against pathogen infection” by Daniel Fisch, Moritz M. Pfleiderer, Eleni Anastasakou, Gillian M. Mackie, Fabian Wendt, Xiangyang Liu, Barbara Clough, Samuel Lara-Reyna, Vesela Encheva, Ambrosius P. Snijders, Hironori Bando, Masahiro Yamamoto, Andrew D. Beggs, Jason Mercer, Avinash R. Shenoy, Bernd Wollscheid, Kendle M. Maslowski, Wojtek P. Galej and Eva-Maria Frickel, 6 October 2023, Science.
DOI: 10.1126/science.adg2253
The study was funded by the Wellcome Trust.
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