Login / Signup

Cu II -mediated stabilisation of DNA duplexes bearing consecutive ethenoadenine lesions and its application to a metal-responsive DNAzyme.

Silpa Chandran RajasreeYusuke TakezawaMitsuhiko Shionoya
Published in: Chemical communications (Cambridge, England) (2022)
Metal-mediated nucleobase pairing can play a central role in the expression of metal-responsive DNA functions. We report the Cu II -mediated stabilisation of DNA duplexes bearing damaged nucleobases, 1, N 6 -ethenoadenine (εA), as metal-binding sites, which was utilised to construct a metal-responsive DNAzyme. Consecutive incorporation of three or more εA-εA mismatch pairs allowed for Cu II -dependent significant duplex stabilisation through metal-mediated εA-Cu II -εA base pairing. Subsequently, a split DNAzyme with three εA-Cu II -εA base pairs was strategically designed. The activity of the εA-modified DNAzyme was enhanced by 5.3-fold upon addition of Cu II ions. This study demonstrates the utility of εA lesions for building metal-responsive DNA architectures.
Keyphrases
  • circulating tumor
  • aqueous solution
  • cell free
  • cancer therapy
  • poor prognosis
  • metal organic framework
  • label free
  • drug delivery
  • quantum dots
  • binding protein