GSK-3-selective inhibitors derived from Tyrian purple indirubins.

نویسندگان

  • Laurent Meijer
  • Alexios-Leandros Skaltsounis
  • Prokopios Magiatis
  • Panagiotis Polychronopoulos
  • Marie Knockaert
  • Maryse Leost
  • Xiaozhou P Ryan
  • Claudia Alin Vonica
  • Ali Brivanlou
  • Rana Dajani
  • Claudia Crovace
  • Cataldo Tarricone
  • Andrea Musacchio
  • S Mark Roe
  • Laurence Pearl
  • Paul Greengard
چکیده

Gastropod mollusks have been used for over 2500 years to produce the "Tyrian purple" dye made famous by the Phoenicians. This dye is constituted of mixed bromine-substituted indigo and indirubin isomers. Among these, the new natural product 6-bromoindirubin and its synthetic, cell-permeable derivative, 6-bromoindirubin-3'-oxime (BIO), display remarkable selective inhibition of glycogen synthase kinase-3 (GSK-3). Cocrystal structure of GSK-3beta/BIO and CDK5/p25/indirubin-3'-oxime were resolved, providing a detailed view of indirubins' interactions within the ATP binding pocket of these kinases. BIO but not 1-methyl-BIO, its kinase inactive analog, also inhibited the phosphorylation on Tyr276/216, a GSK-3alpha/beta activation site. BIO but not 1-methyl-BIO reduced beta-catenin phosphorylation on a GSK-3-specific site in cellular models. BIO but not 1-methyl-BIO closely mimicked Wnt signaling in Xenopus embryos. 6-bromoindirubins thus provide a new scaffold for the development of selective and potent pharmacological inhibitors of GSK-3.

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عنوان ژورنال:
  • Chemistry & biology

دوره 10 12  شماره 

صفحات  -

تاریخ انتشار 2003