AI tool enables rapid and cost-effective drug discovery


Tuesday, 02 July, 2024


AI tool enables rapid and cost-effective drug discovery

Australian researchers, led by Monash University, have invented a new artificial intelligence (AI) tool which has the potential to reshape virtual screening in early-stage drug discovery and enhance scientists’ ability to identify potential new medicines.

Although computational methods within drug discovery are well established, there is a clear gap when it comes to novel AI tools capable of rapidly, robustly and cost-effectively predicting the strength of interactions between molecules and proteins — a critical step in the drug discovery process. The Australian invention ‘PSICHIC’ (PhySIcoCHemICal) brings together expertise at the interface of computing technology and drug discovery to offer an entirely new approach.

Documented in the journal Nature Machine Intelligence, PSICHIC uses only sequence data, alongside AI, to decode protein–molecule interactions with state-of-the-art accuracy, while eliminating the need for costly and less accurate processes such as 3D structures. As noted by co-lead author Dr Lauren May, from the Monash Institute of Pharmaceutical Sciences (MIPS), the research team has already demonstrated that PSICHIC can effectively screen new drug candidates and perform selectivity profiling.

“Comparison of experimental and AI predictions of a large compound library against the A1 receptor — a potential therapeutic target for many diseases — demonstrated PSICHIC could effectively screen and identify a novel drug candidate,” May said. “Moreover, PSICHIC was able to distinguish the functional effects of the compound or, in other words, the way in which the drug might affect our bodies.

“There is enormous potential for AI to completely change the drug discovery landscape. We foresee PSICHIC reshaping virtual screening and deepening our understanding of protein–molecule interactions.”

Lead author Professor Geoff Webb, from Monash’s Department of Data Science and Artificial Intelligence, said while other methods for predicting protein–molecule interactions already exist, they can be expensive and falter in their ability to predict a drug’s functional effects.

“The application of AI approaches to enhance the affordability and accuracy of drug discovery is a rapidly expanding area,” he said. “With PSICHIC, our team has eliminated the need for 3D structures to map protein–molecule interactions, which is a costly and often restrictive requirement.

“Instead, PSICHIC identifies the unique ‘fingerprints’ of specific protein–molecule interactions by applying AI to analyse thousands of protein-molecule interactions, resulting in faster and more effective screening of drug compounds without the need for rendering protein or molecule structures in high-resolution 3D.”

Co-lead author Dr Anh Nguyen, also from MIPS, emphasised the importance of these interactions, noting that drugs exert their intended effects by selectively interacting with specific proteins. “There have been significant global efforts to develop new AI-based methods to accurately determine how a molecule might behave when it interacts with its protein target — after all, this is the core building block to making medicines,” she said.

First author Huan Yee Koh, a PhD candidate from Monash’s Faculty of Information Technology, said that AI has the potential to dramatically improve the robustness, efficiency and cost at multiple stages during the drug discovery process. “However, since many AI systems fundamentally rely on pattern matching, these systems can suffer from unrestrained degrees of freedom. This can lead to memorisation of previously known patterns rather than learning the underlying mechanisms of protein-ligand interactions, ultimately hindering the discovery of novel drugs,” he said.

“PSICHIC addresses this issue by incorporating physicochemical constraints into its AI model when learning from sequence data. This enables PSICHIC to attain capabilities in decoding the mechanisms underlying protein–ligand interactions directly from sequence data, bypassing the need for costly structures and making drug discovery more efficient and reliable.”

Co-lead author Professor Shirui Pan, an ARC Future Fellow with the School of Information and Communication Technology at Griffith University, said the fact PSICHIC requires only sequence data for operation means it is uniquely accessible.

“Compared to previous deep sequence-based methods, this approach provides a more faithful representation of the underlying protein–molecule interactions, thereby closing the performance gap between sequence-based methods and structure-based or complex-based methods,” he concluded.

The PSICHIC team has made their data, code and optimised model available to the broader scientific community. For more information, visit www.psichicserver.com.

Image credit: iStock.com/Yuuji

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