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Oncogene. 2016 Sep 19. doi: 10.1038/onc.2016.321. [Epub ahead of print]

Full-length p53 tetramer bound to DNA and its quaternary dynamics.

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  • 1Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla, CA, USA.
  • 2National Biomedical Computation Resource, University of California, San Diego, La Jolla, CA, USA.

Abstract

P53 is a major tumor suppressor that is mutated and inactivated in ~50% of all human cancers. Thus, reactivation of mutant p53 using small molecules has been a long sought-after anticancer therapeutic strategy. Full structural characterization of the full-length oligomeric p53 is challenging because of its complex architecture and multiple highly flexible regions. To explore p53 structural dynamics, here we developed a series of atomistic integrative models with available crystal structures of the full-length p53 (fl-p53) tetramer bound to three different DNA sequences: a p21 response element, a puma response element and a nonspecific DNA sequence. Explicitly solvated, all-atom molecular dynamics simulations of the three complexes (totaling nearly 1 μs of aggregate simulation time) yield final structures consistent with electron microscopy maps and, for the first time, show the direct interactions of the p53 C-terminal with DNA. Through a collective principal component analysis, we identify sequence-dependent differential quaternary binding modes of the p53 tetramer interfacing with DNA. Additionally, L1 loop dynamics of fl-p53 in the presence of DNA is revealed, and druggable pockets of p53 are identified via solvent mapping to aid future drug discovery studies.Oncogene advance online publication, 19 September 2016; doi:10.1038/onc.2016.321.

PMID:
27641333
DOI:
10.1038/onc.2016.321
[PubMed - as supplied by publisher]
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