Functional
DNAs are valuable molecular tools in chemical biology
and analytical chemistry but suffer from low activities due to their
limited chemical functionalities. Here, we present a chemoenzymatic
method for site-specific installation of diverse functional groups
on DNA, and showcase the application of this method to enhance the
catalytic activity of a DNA catalyst. Through chemoenzymatic introduction
of distinct chemical groups, such as hydroxyl, carboxyl, and benzyl,
at specific positions, we achieve significant enhancements in the
catalytic activity of the RNA-cleaving deoxyribozyme 10–23.
A single carboxyl modification results in a 100-fold increase, while
dual modifications (carboxyl and benzyl) yield an approximately 700-fold
increase in activity when an RNA cleavage reaction is catalyzed on
a DNA–RNA chimeric substrate. The resulting dually modified
DNA catalyst, CaBn, exhibits a k
obs of
3.76 min–1 in the presence of 1 mM Mg2+ and can be employed for fluorescent imaging of intracellular magnesium
ions. Molecular dynamics simulations reveal the superior capability
of CaBn to recruit magnesium ions to metal-ion-binding site 2 and
adopt a catalytically competent conformation. Our work provides a
broadly accessible strategy for DNA functionalization with diverse
chemical modifications, and CaBn offers a highly active DNA catalyst
with immense potential in chemistry and biotechnology.