Researchers at the University of Toronto have developed a deep-learning model that can predict all possible shapes of peptides - chains of amino acids that are shorter than proteins, but perform similar biological functions.
Called PepFlow, the model combines machine learning and physics to model the range of folding patterns that a peptide can assume based on its energy landscape.
Peptides, unlike proteins, are dynamic molecules that can take on a range of conformations. They are involved in many biological processes that are of keen interest to researchers who are developing therapeutics.
"We haven't been able to model the full range of conformations for peptides until now," said Osama Abdin, first author on the study and recent PhD graduate of molecular genetics at U of T's Donnelly Centre for Cellular and Biomolecular Research. "PepFlow leverages deep-learning to capture the precise and accurate conformations of a peptide within minutes.
"There's potential with this model to inform drug development through the design of peptides that act as binders."
The study was recently published in the journal Nature Machine Intelligence.
A peptide's role in the human body is directly linked to how it folds since its 3D structure determines the way it binds and interacts with other molecules.
"Peptides were the focus of the PepFlow model because they are very important biological molecules and they are naturally very dynamic, so we need to model their different conformations to understand their function," said Philip M. Kim, the study's principal investigator and a professor at the Donnelly Centre. "They're also important as therapeutics, as can be seen by the GLP1 analogues, like Ozempic, used to treat diabetes and obesity."
Peptides are also cheaper to produce than their larger protein counterparts, said Kim, who is also a professor of computer science in U of T's Faculty of Arts & Science and a professor of molecular genetics in the Temerty Faculty of Medicine.
The new model expands on the capabilities of AlphaFold, the leading Google DeepMind AI system for predicting protein structure. It does this by generating a range of conformations for a given peptide. Taking inspiration from highly advanced physics-based machine learning models, PepFlow can also model peptide structures that take on unusual formations, including the ring-like structure that results from a process called macrocyclization. Peptide macrocycles are currently a highly promising venue for drug development.
"It took two-and-a-half years to develop PepFlow and one month to train it, but it was worthwhile to move to the next frontier beyond models that only predict one structure of a peptide," Abdin said.
There are, however, limitations given that PepFlow represents the first version of a new model. The study authors noted a number of ways in which PepFlow could be improved, including training the model with explicit data for solvent atoms, which would dissolve the peptides to form a solution, and for constraints on the distance between atoms in ring-like structures.
Yet, even as a first version, the researchers say PepFlow is a comprehensive and efficient model with potential for furthering the development of treatments that depend on peptide binding to activate or inhibit biological processes.
"Modelling with PepFlow offers insight into the real energy landscape of peptides," said Abdin.
The research was supported by the Canadian Institutes of Health Research and the Natural Sciences and Engineering Research Council of Canada.
