1. Academic Validation
  2. N (6)-substituted AMPs inhibit mammalian deoxynucleotide N-hydrolase DNPH1

N (6)-substituted AMPs inhibit mammalian deoxynucleotide N-hydrolase DNPH1

  • PLoS One. 2013 Nov 19;8(11):e80755. doi: 10.1371/journal.pone.0080755.
Claire Amiable 1 Sylvie Pochet André Padilla Gilles Labesse Pierre Alexandre Kaminski
Affiliations

Affiliation

  • 1 Institut Pasteur, Unité de Chimie et Biocatalyse, Paris, France ; CNRS, UMR3523, Paris, France ; Université Paris Descartes Sorbonne Paris Cité, Paris, France.
Abstract

The gene dnph1 (or rcl) encodes a hydrolase that cleaves the 2'-deoxyribonucleoside 5'-monophosphate (dNMP) N-glycosidic bond to yield a free nucleobase and 2-deoxyribose 5-phosphate. Recently, the crystal structure of rat DNPH1, a potential target for anti-cancer therapies, suggested that various analogs of AMP may inhibit this Enzyme. From this result, we asked whether N (6)-substituted AMPs, and among them, cytotoxic Cytokinin riboside 5'-monophosphates, may inhibit DNPH1. Here, we characterized the structural and thermodynamic aspects of the interactions of these various analogs with DNPH1. Our results indicate that DNPH1 is inhibited by cytotoxic cytokinins at concentrations that inhibit cell growth.

Figures