RNA cleavage by a DNA enzyme with extended chemical functionality

J Am Chem Soc. 2000 Mar 22;122(11):2433-9. doi: 10.1021/ja993688s.

Abstract

In vitro selection techniques were applied to the development of a DNA enzyme that contains three catalytically essential imidazole groups and catalyzes the cleavage of RNA substrates. Nucleic acid libraries for selection were constructed by polymerase-catalyzed incorporation of C5-imidazole-functionalized deoxyuridine in place of thymidine. Chemical synthesis was used to define a minimized catalytic domain composed of only 12 residues. The catalytic domain forms a compact hairpin structure that displays the three imidazole-containing residues. The enzyme can be made to cleave RNAs of almost any sequence by simple alteration of the two substrate-recognition domains that surround the catalytic domain. The enzyme operates with multiple turnover in the presence of micromolar concentrations of Zn2+, exhibiting saturation kinetics and a catalytic rate of >1 min-1. The imidazole-containing DNA enzyme, one of the smallest known nucleic acid enzymes, combines the substrate-recognition properties of nucleic acid enzymes and the chemical functionality of protein enzymes in a molecule that is small, yet versatile and catalytically efficient.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Base Composition
  • Base Sequence
  • Catalysis
  • Cations, Divalent
  • DNA / chemistry*
  • DNA / metabolism
  • Deoxyuridine / analogs & derivatives*
  • Endoribonucleases / chemical synthesis*
  • Endoribonucleases / chemistry
  • Endoribonucleases / metabolism
  • Hydrogen-Ion Concentration
  • Imidazoles / chemistry*
  • Kinetics
  • Metals / chemistry
  • Metals / metabolism
  • RNA / chemistry*
  • RNA / metabolism
  • RNA, Catalytic
  • Substrate Specificity
  • Zinc / chemistry*

Substances

  • Cations, Divalent
  • Imidazoles
  • Metals
  • RNA, Catalytic
  • RNA
  • DNA
  • Endoribonucleases
  • Zinc
  • Deoxyuridine