Interenzyme Substrate Diffusion for an Enzyme Cascade Organized on Spatially Addressable DNA Nanostructures

被引:581
|
作者
Fu, Jinglin [1 ,2 ]
Liu, Minghui [2 ,3 ]
Liu, Yan [2 ,3 ]
Woodbury, Neal W. [1 ,3 ]
Yan, Hao [2 ,3 ]
机构
[1] Arizona State Univ, Ctr Innovat Med, Biodesign Inst, Tempe, AZ 85287 USA
[2] Arizona State Univ, Ctr Single Mol Biophys, Tempe, AZ 85287 USA
[3] Arizona State Univ, Dept Chem & Biochem, Tempe, AZ 85287 USA
基金
美国国家科学基金会;
关键词
HYDROGEN-PEROXIDE; WATER; PROTEINS; ORIGAMI; SITE; H2O2;
D O I
10.1021/ja300897h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:5516 / 5519
页数:4
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