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A DNA-conjugated small molecule catalyst enzyme mimic for site-selective ester hydrolysis† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c7sc04554a

A DNA-imidazole conjugate, designed to mimic enzyme function, site-selectively hydrolyzes a target ester, but not other esters, with >100-fold rate enhancement compared to free imidazole. The challenge of site-selectivity must be overcome in many chemical research contexts, including selective fu...

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Bibliographic Details
Published in:Chemical science (Cambridge) 2018-01, Vol.9 (8), p.2105-2112
Main Authors: Flanagan, Moira L., Arguello, A. Emilia, Colman, Drew E., Kim, Jiyeon, Krejci, Jesse N., Liu, Shimu, Yao, Yueyu, Zhang, Yu, Gorin, David J.
Format: Article
Language:English
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Summary:A DNA-imidazole conjugate, designed to mimic enzyme function, site-selectively hydrolyzes a target ester, but not other esters, with >100-fold rate enhancement compared to free imidazole. The challenge of site-selectivity must be overcome in many chemical research contexts, including selective functionalization in complex natural products and labeling of one biomolecule in a living system. Synthetic catalysts incorporating molecular recognition domains can mimic naturally-occurring enzymes to direct a chemical reaction to a particular instance of a functional group. We propose that DNA-conjugated small molecule catalysts (DCats), prepared by tethering a small molecule catalyst to a DNA aptamer, are a promising class of reagents for site-selective transformations. Specifically, a DNA-imidazole conjugate able to increase the rate of ester hydrolysis in a target ester by >100-fold compared with equimolar untethered imidazole was developed. Other esters are unaffected. Furthermore, DCat-catalyzed hydrolysis follows enzyme-like kinetics and a stimuli-responsive variant of the DCat enables programmable “turn on” of the desired reaction.
ISSN:2041-6520
2041-6539
DOI:10.1039/c7sc04554a