A new accurate computational method designed to enhance drug target stability

A new accurate computational method designed to enhance drug target stability
Structures of GPCRs solved with stabilizing mutations predicted by CompoMug. (a) serotonin 5-HT2c receptor (PDB:), (b) frizzled FZD4 receptor, © prostaglandin EP3 receptor and (d) cannabinoid CB2 receptor. Stabilizing amino acid residues predicted with CompoMug are shown as sticks, with those mutations that were included into the final crystallized construct colored green. Credit: Petr Popov et al./Current Opinion in Structural Biology

Scientists from the Moscow Institute of Physics and Technology (MIPT), the Skolkovo Institute of Science and Technology (Skoltech), and the University of Southern California (USC) have developed a new computational method for the design of thermally stable G protein-coupled receptors (GPCR) that are of great help in creating new drugs. The method has already proved useful in obtaining the structures of several principal human receptors. An overview of the new method was published in Current Opinion on Structural Biology.

Receptors are molecules that capture and transmit signals and play a key role in the human body regulation. GPCRs are among the best-known human protein families involved in vision, olfaction, immune response and brain processes, making them an important drug target. For a receptor to serve as a target, the researchers need to understand its structure in great detail, just as a locksmith needs to know the lock's inner structure to make a key that fits. Studying a receptor that becomes unstable when detached from the is a much more challenging task, which is largely facilitated by the that help to accurately predict the receptor's soft spots and the changes that will make it more stable.

"The structural studies of GPCRs are of high scientific and applied value, since these proteins are the target for 30 to 40 percent of drugs. Our method relies on several approaches, including , molecular modeling, and bioinformatics, that are tailored specifically to GPCRs. These approaches are complementary, which enables effectively predicting the smallest possible changes that can enhance the receptor's stability and make it easier to obtain its ," explains professor Petr Popov of MIPT's Laboratory of Structural Biology of G Protein-Coupled Receptors and the Skoltech Center for Computational and Data-Intensive Science and Engineering.

The new method developed at MIPT, Skoltech, and USC allowed researchers to obtain the structures of four important human , including the cannabinoid receptor involved in brain signal transmission and pain perception, and the prostaglandin receptor implicated in inflammatory processes in the human body. The results of the study were published in the top international science journals Cell and Nature Chemical Biology.


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More information: Petr Popov et al, Computational design for thermostabilization of GPCRs, Current Opinion in Structural Biology (2019). DOI: 10.1016/j.sbi.2019.02.010
Journal information: Cell , Nature Chemical Biology

Citation: A new accurate computational method designed to enhance drug target stability (2019, April 1) retrieved 26 August 2019 from https://phys.org/news/2019-04-accurate-method-drug-stability.html
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