Scientific communities all over the world have been challenged with developing new antimicrobials to safeguard the population from infections and dreadful diseases. The research arm of the U.S. Department of Defense, the Defense Advanced Research Program Agency, or DARPA, is known for taking on out-sized challenges such as this. And so, they put out a call for researchers to figure out how to make at least 1000 doses to any unknown pathogen - in a week.
‘The new class of antimicrobials, called synbodies can be developed by pre-screening a large number of pathogens on the microarray and find 100 peptides so that any pathogen screened would bind to two or more peptides.’An ASU team was one of the few that rose to this challenge. "As far as we know we were the only team to figure out how to do this for any pathogen - virus or bacterium," said research leader Stephen Albert Johnston, who directs the ASU Biodesign Institute's Center for Innovations in Medicine and is a professor in the School of Life Sciences.
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Antibodies are large, Y-shaped proteins produced by the human immune system to ward off foreign invaders. Our bodies mount this defense rapidly, especially if they have seen the invader before, producing the needed antibody within days of infection.
But to make them in the lab, antibodies specific for just one invader can take months, and be an expensive proposition. Johnston wanted to mimic nature's approach while dramatically reducing the antimicrobial discovery and production time.
For the past decade, Johnston's team has been a pioneer in developing lab-made versions that focus on just the business end of antibodies, critical pathogen recognition elements, called synthetic antibodies, or synbodies.
"Our solution to save time was to pre-screen a large number of pathogens on the microarray and find 100 peptides that would be diverse enough so that any pathogen screened would bind to two or more peptides," said Chris Diehnelt, an associate research professor in Johnston's center who oversaw the lab experiments.
They could stockpile large stocks of these 100 peptides in advance so that 1,000 or more doses of a therapeutic could be quickly produced, screening the best candidates that block a given pathogen. These candidates are then produced in large amounts, purified and tested in mice for acute toxicity so that the whole process is completed in a week.
For their proof-of-concept, they screened a total of 21 different viruses and bacteria against their synbody arrays. "We found that the majority of the peptides recognized one pathogen," said Diehnelt. In addition, they tested their system against two unknown pathogens that were not used in the study. "The data showed that this array can potentially identify binding peptides for any given pathogen," said Diehnelt.
A shot in the arm
"With this approach, dozens or even hundreds of synbodies can be produced in a day," said Johnston. The best candidates are quickly evaluated both for effective killing and toxicity to humans and can be produced on a large scale.
Finally, their system was tested against two societal scourges and major worldwide health concerns: a potentially pandemic flu strain (H1N1 influenza) as a viral test and a bacterium that causes surgery-related infections S. epidermidis.
"Our data indicate that a new virus or bacterium can be screened against the small peptide library to discover binding peptides that can be converted into neutralizing antiviral and antibacterial synbodies in a rapid manner," said Diehnelt.
The next steps would be to prepare the final product for an IV delivery, and to scale up the system to produce enough product for a population-wide use should the next Ebola, Zika or unanticipated outbreak occur.
"One key, unique feature of our synbody technology is that the same platform can produce synbodies with direct antibiotic or antiviral activity, and we can do it at a fraction of the potential cost as current, commercially produced therapeutic antibodies," said Johnston.