LA BioMed scientists discover common blueprint for protein antibiotics

March 19, 2019

A discovery by researchers at the Los Angeles Biomedical Research Institute (LA BioMed) has uncovered a common blueprint for proteins that have antimicrobial properties. This finding opens the door to design and development of a new generation of anti-infectives active against pathogens that have become resistant to conventional antibiotics.

The findings are published in the Proceedings of the National Academy of Sciences of the United States of America, in a paper titled “A Unifying Structural Signature of Eukaryotic α-helical Host Defense Peptides.”

The discovery was made by Dr. Nannette Yount and Dr. Michael Yeaman, who found that certain small proteins, called peptides, have antimicrobial activity if they contain a specific structural signature consisting of a conserved amino acid pattern that forms a three-dimensional shape known as an alpha-helix.

Yount and Yeaman discovered and characterized the alpha-core signature, and then used it to mine the database of all known proteins and peptides. In doing so, they found thousands of proteins never before known to have antimicrobial activity. The team then synthesized examples of the newly discovered peptides demonstrating that they have potent antimicrobial activity against infective microbes that resist even the most modern antibiotics.

Together, they applied state-of-the-art artificial intelligence and machine learning methods to verify how the alpha-core signature encompasses features of peptides known to exert strong antimicrobial activity. This is an example of how medicine, bioengineering and computational modeling can work toward improved health outcomes.

One significant advancement the LA BioMed team discovered is that it can be used to engineer fundamentally new types of anti-infectives designed to prevent or treat even the most antibiotic-resistant microbes – superbugs – commonly found in hospitals and other healthcare facilities, which are now threatening U.S. public health.

“We are already nearing the clinic with molecules that incorporate this molecular signature and this discovery opens the door to thousands of new templates from which we can develop newer, potentially even better anti-infectives,” Yeaman said.

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