Spatially addressable DNA nanostructures facilitate the
self-assembly
of heterogeneous elements with precisely controlled patterns. Here
we organized discrete glucose oxidase (GOx)/horseradish peroxidase
(HRP) enzyme pairs on specific DNA origami tiles with controlled interenzyme
spacing and position. The distance between enzymes was systematically
varied from 10 to 65 nm, and the corresponding activities were evaluated.
The study revealed two different distance-dependent kinetic processes
associated with the assembled enzyme pairs. Strongly enhanced activity
was observed for those assemblies in which the enzymes were closely
spaced, while the activity dropped dramatically for enzymes as little
as 20 nm apart. Increasing the spacing further resulted in a much
weaker distance dependence. Combined with diffusion modeling, the
results suggest that Brownian diffusion of intermediates in solution
governed the variations in activity for more distant enzyme pairs,
while dimensionally limited diffusion of intermediates across connected
protein surfaces contributed to the enhancement in activity for closely
spaced GOx/HRP assemblies. To further test the role of limited dimensional
diffusion along protein surfaces, a noncatalytic protein bridge was
inserted between GOx and HRP to connect their hydration shells. This
resulted in substantially enhanced activity of the enzyme pair