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bioRxiv · 10.1101/2024.10.12.618044

mTOR variants activation discovers PI3K-like cryptic pocket, expanding allosteric, mutant-selective inhibitor designs

Liu, Y.·Zhang, W.·Jang, H.·Nussinov, R.
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Abstract

mTOR plays a crucial role in PI3K/AKT/mTOR signaling. We hypothesized that mTOR activation mechanisms driving oncogenesis can advise effective therapeutic designs. To test this, we combined cancer genomic analysis with extensive molecular dynamics simulations of mTOR oncogenic variants. We observed that conformational changes within mTOR kinase domain are associated with multiple mutational activation events. The mutations disturb the -packing formed by the kAL, k3, k9, k9b, and k10 helices in the kinase domain creating cryptic pocket. Its opening correlates with opening of the catalytic cleft, including active site residues realignment, favoring catalysis. The cryptic pocket created by disrupted -packing coincides with the allosteric pocket in PI3K can be harmoniously fitted by the PI3K allosteric inhibitor RLY-2608, suggesting that analogous drugs designed based on RLY-2608 can restore the packed -structure, resulting in mTOR inactive conformation. Our results exemplify that knowledge of detailed kinase activation mechanisms can inform innovative allosteric inhibitor development.

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Liu, Y., Zhang, W., Jang, H., Nussinov, R.. 2024-10-15. mTOR variants activation discovers PI3K-like cryptic pocket, expanding allosteric, mutant-selective inhibitor designs. https://doi.org/10.1101/2024.10.12.618044

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