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J Am Chem Soc. 2012 Mar 28;134(12):5516-9. doi: 10.1021/ja300897h. Epub 2012 Mar 16.

Interenzyme substrate diffusion for an enzyme cascade organized on spatially addressable DNA nanostructures.

Author information

1
Center for Single Molecule Biophysics, Arizona State University, Tempe, Arizona 85287, United States.

Abstract

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.

PMID:
22414276
PMCID:
PMC3319985
DOI:
10.1021/ja300897h
[Indexed for MEDLINE]
Free PMC Article

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