Mechanism of inhibition of human cytomegalovirus replication by oxetanocin G

Biochem Biophys Res Commun. 1991 Apr 30;176(2):805-12. doi: 10.1016/s0006-291x(05)80257-8.

Abstract

Oxetanocin G(9-(2-deoxy-2-hydroxymethyl-beta-D-erythro-oxetanosyl)guanine, OXT-G) is a potent and selective agent against human cytomegalovirus (HCMV). In this study we synthesized the triphosphate form of OXT-G, OXT-GTP, and examined its effect on the activities of HCMV DNA polymerase, herpes simplex type 2 (HSV-2) DNA polymerase and human DNA polymerase alpha. OXT-GTP was found to inhibit all these polymerases in a competitive manner with respect to dGTP. The Km for dGTP and the Ki for OXT-GTP of HCMV DNA polymerase were 0.86 and 0.53 mu M, respectively, while the corresponding values of DNA polymerase alpha were 2.2 and 3.6 mu M, respectively. HPLC analysis using [3H]OXT-G also revealed that OXT-G was converted to its triphosphate form 7- to 8-fold more efficiently in HCMV-infected cells than in uninfected cells. The results suggest that both the preferential phosphorylation of OXT-G in HCMV-infected cells and the preferential inhibition of HCMV DNA polymerase by OXT-GTP may contribute towards the selective activity of OXT-G against HCMV replication.

MeSH terms

  • Antiviral Agents / pharmacology*
  • Chromatography, High Pressure Liquid
  • Cytomegalovirus / drug effects
  • Cytomegalovirus / enzymology
  • Cytomegalovirus / growth & development*
  • DNA-Directed DNA Polymerase / metabolism
  • Fibroblasts / drug effects
  • Fibroblasts / physiology
  • Guanine / analogs & derivatives*
  • Guanine / pharmacology
  • Guanosine Triphosphate / analogs & derivatives*
  • Guanosine Triphosphate / metabolism
  • Guanosine Triphosphate / pharmacology
  • Humans
  • Phosphorylation
  • Virus Replication / drug effects*

Substances

  • Antiviral Agents
  • oxetanocin G
  • oxetanocin guanosine triphosphate
  • Guanine
  • Guanosine Triphosphate
  • DNA-Directed DNA Polymerase