| Literature DB >> 26919202 |
Jack L-Y Chen1, Cristian Pezzato1, Paolo Scrimin1, Leonard J Prins2.
Abstract
Enantioselectivity in RNA cleavage by a synthetic metalloenzyme has been demonstrated for the first time. Thiols containing chiral Zn(II) -binding head groups have been self-assembled on the surface of gold nanoparticles. This results in the spontaneous formation of chiral bimetallic catalytic sites that display different activities (kcat ) towards the enantiomers of an RNA model substrate. Substrate selectivity is observed when the nanozyme is applied to the cleavage of the dinucleotides UpU, GpG, ApA, and CpC, and remarkable differences in reactivity are observed for the cleavage of the enantiomerically pure dinucleotide UpU.Entities:
Keywords: chirality; enzyme mimics; nanozymes; self-assembly; transphosphorylation
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Year: 2016 PMID: 26919202 DOI: 10.1002/chem.201600853
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236