TY - JOUR
T1 - Multi-enzyme complexes on DNA scaffolds capable of substrate channelling with an artificial swinging arm
AU - Fu, Jinglin
AU - Yang, Yuhe Renee
AU - Johnson-Buck, Alexander
AU - Liu, Minghui
AU - Liu, Yan
AU - Walter, Nils G.
AU - Woodbury, Neal
AU - Yan, Hao
N1 - Funding Information:
This work was supported by an Army Research Office MURI award (no. W911NF-12-1-0420 to H.Y., N.G.W. and N.W.W.), a National Science Foundation grant (no. 1033222 to N.W.W. and H.Y.) and an Army Research Office grant (no. W911NF-11-1-0137 to H.Y. and Y.L.). H.Y. is supported by the Presidential Strategic Initiative Fund from Arizona State University. The authors are grateful to J. Nangreave for her help in editing the manuscript and W. Li for his assistance with the FastScan AFM.
PY - 2014/7
Y1 - 2014/7
N2 - Swinging arms are a key functional component of multistep catalytic transformations in many naturally occurring multi-enzyme complexes. This arm is typically a prosthetic chemical group that is covalently attached to the enzyme complex via a flexible linker, allowing the direct transfer of substrate molecules between multiple active sites within the complex. Mimicking this method of substrate channelling outside the cellular environment requires precise control over the spatial parameters of the individual components within the assembled complex. DNA nanostructures can be used to organize functional molecules with nanoscale precision and can also provide nanomechanical control. Until now, protein-DNA assemblies have been used to organize cascades of enzymatic reactions by controlling the relative distance and orientation of enzymatic components or by facilitating the interface between enzymes/cofactors and electrode surfaces. Here, we show that a DNA nanostructure can be used to create a multi-enzyme complex in which an artificial swinging arm facilitates hydride transfer between two coupled dehydrogenases. By exploiting the programmability of DNA nanostructures, key parameters including position, stoichiometry and inter-enzyme distance can be manipulated for optimal activity.
AB - Swinging arms are a key functional component of multistep catalytic transformations in many naturally occurring multi-enzyme complexes. This arm is typically a prosthetic chemical group that is covalently attached to the enzyme complex via a flexible linker, allowing the direct transfer of substrate molecules between multiple active sites within the complex. Mimicking this method of substrate channelling outside the cellular environment requires precise control over the spatial parameters of the individual components within the assembled complex. DNA nanostructures can be used to organize functional molecules with nanoscale precision and can also provide nanomechanical control. Until now, protein-DNA assemblies have been used to organize cascades of enzymatic reactions by controlling the relative distance and orientation of enzymatic components or by facilitating the interface between enzymes/cofactors and electrode surfaces. Here, we show that a DNA nanostructure can be used to create a multi-enzyme complex in which an artificial swinging arm facilitates hydride transfer between two coupled dehydrogenases. By exploiting the programmability of DNA nanostructures, key parameters including position, stoichiometry and inter-enzyme distance can be manipulated for optimal activity.
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U2 - 10.1038/nnano.2014.100
DO - 10.1038/nnano.2014.100
M3 - Article
C2 - 24859813
AN - SCOPUS:84904068531
SN - 1748-3387
VL - 9
SP - 531
EP - 536
JO - Nature Nanotechnology
JF - Nature Nanotechnology
IS - 7
ER -