Tumor Suppressor p16~(INK4A): Determination of Solution Structure and Analyses of Its Interaction with Cyclin-Dependent Kinase 4

摘要

The solution structure of the tumor suppressor p16~(INK4A) has been determined by NMR, and important recognition regions of both cdk4 and p16~(INK4A) have been identified. The tertiary structure of p16~(INK4A) contains four helix-turn-helix motifs liked by three loops. Twelve tumorigenic mutants of p16~(INK4A) have been constructed and analyzed for their structure and activity, and new mutants have been designed rationally. A fragment of 58 residues at the N terminus of cdk4 important for p16~(INK4A) binding has been identified. The importance of this region was further verified by mutational analysis of cdk4. These results and docking experiments have been used to assess possible modes of binding between p16~(INK4A) and cdk4.