Literature DB >> 22367854

Supramolecular tandem enzyme assays.

Roy N Dsouza1, Andreas Hennig, Werner M Nau.   

Abstract

We conceptualize a novel approach towards enzyme assays based on the reversible and competitive binding of a fluorescent dye and the substrate as well as product of an enzymatic reaction to a macrocyclic host. This method was termed "supramolecular tandem assay", and has been applied to inhibitor and activator screening, sensor array development, and enantiomeric excess determination of amino acids. The simple and rapid read-out by fluorescence allows their straightforward implementation into high-throughput screening.
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Year:  2012        PMID: 22367854     DOI: 10.1002/chem.201103364

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  20 in total

1.  Site-Selective Sensing of Histone Methylation Enzyme Activity via an Arrayed Supramolecular Tandem Assay.

Authors:  Yang Liu; Lizeth Perez; Adam D Gill; Magi Mettry; Lin Li; Yinsheng Wang; Richard J Hooley; Wenwan Zhong
Journal:  J Am Chem Soc       Date:  2017-08-08       Impact factor: 15.419

2.  Acyclic Cucurbit[n]uril-Type Receptors: Optimization of Electrostatic Interactions for Dicationic Guests.

Authors:  Xiaoyong Lu; Sandra A Zebaze Ndendjio; Peter Y Zavalij; Lyle Isaacs
Journal:  Org Lett       Date:  2020-06-10       Impact factor: 6.005

3.  Selective discrimination and classification of G-quadruplex structures with a host-guest sensing array.

Authors:  Junyi Chen; Briana L Hickey; Linlin Wang; Jiwon Lee; Adam D Gill; Alessia Favero; Roberta Pinalli; Enrico Dalcanale; Richard J Hooley; Wenwan Zhong
Journal:  Nat Chem       Date:  2021-04-01       Impact factor: 24.427

4.  Glycoluril-Derived Molecular Clips are Potent and Selective Receptors for Cationic Dyes in Water.

Authors:  Nengfang She; Damien Moncelet; Laura Gilberg; Xiaoyong Lu; Vladimir Sindelar; Volker Briken; Lyle Isaacs
Journal:  Chemistry       Date:  2016-08-05       Impact factor: 5.236

5.  Cationic acyclic cucurbit[n]uril-type containers: synthesis and molecular recognition toward nucleotides.

Authors:  David Sigwalt; Peter Y Zavalij; Lyle Isaacs
Journal:  Supramol Chem       Date:  2016-04-13       Impact factor: 1.688

6.  Acyclic Cucurbit[n]uril-type Receptors: Preparation, Molecular Recognition Properties and Biological Applications.

Authors:  Shweta Ganapati; Lyle Isaacs
Journal:  Isr J Chem       Date:  2017-11-14       Impact factor: 3.333

7.  Acyclic cucurbit[n]uril-type molecular containers: influence of glycoluril oligomer length on their function as solubilizing agents.

Authors:  Laura Gilberg; Ben Zhang; Peter Y Zavalij; Vladimir Sindelar; Lyle Isaacs
Journal:  Org Biomol Chem       Date:  2015-04-07       Impact factor: 3.876

8.  Acyclic Cucurbit[n]uril-Type Molecular Containers: Influence of Linker Length on Their Function as Solubilizing Agents.

Authors:  David Sigwalt; Damien Moncelet; Shane Falcinelli; Vijaybabu Mandadapu; Peter Y Zavalij; Anthony Day; Volker Briken; Lyle Isaacs
Journal:  ChemMedChem       Date:  2016-03-15       Impact factor: 3.466

9.  Acyclic CB[n]-type molecular containers: effect of solubilizing group on their function as solubilizing excipients.

Authors:  Ben Zhang; Peter Y Zavalij; Lyle Isaacs
Journal:  Org Biomol Chem       Date:  2014-04-21       Impact factor: 3.876

10.  Acyclic Cucurbituril Featuring Pendant Cyclodextrins.

Authors:  Ming Cheng; Lyle Isaacs
Journal:  Supramol Chem       Date:  2021-05-31       Impact factor: 1.688

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