期刊
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY
卷 38, 期 1, 页码 84-99出版社
TAYLOR & FRANCIS LTD
DOI: 10.1080/14756366.2022.2135511
关键词
Cyclin-dependent kinase 2; cyclin-dependent kinase 6; binding selectivity; cross-correlation analysis
Multiple short molecular dynamics simulations and calculations were used to investigate the binding selectivity mechanism of inhibitors X64, X3A, and 4 AU towards CDK2 and CDK6. The study found that CDK6 has stronger local structural and global flexibility compared to CDK2. The calculated binding free energies showed that the compensation between binding enthalpy and entropy is a key factor driving selectivity of inhibitors towards CDK2 over CDK6.
Understanding selectivity-dependent molecular mechanism of inhibitors towards CDK2 over CDK6 is prominent for improving drug design towards the CDK family. Multiple short molecular dynamics (MD) simulations combined with MM-GBSA approach are adopted to investigate molecular mechanism on binding selectivity of inhibitors X64, X3A, and 4 AU to CDK2 and CDK6. The RMSF analysis and calculations of molecular surface areas indicate that local structural and global flexibility of CDK6 are stronger than that of CDK2. Based on dynamics cross-correlation maps (DCCMs), motion modes of CDK2 and CDK6 produce difference due to associations of X64, X3A, and 4 AU. The calculated binding free energies (BFEs) demonstrate that the compensation between binding enthalpy and entropy of X64, X34, and 4 AU is a key force driving selectivity of inhibitors towards CDK2 over CDK6. This work provides valuable information for designing highly selective inhibitors towards CDK2 and CDK6 and further promotes identification of efficient anticancer drugs in the future.
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