Literature DB >> 21552586

"Turn-on" fluorescent sensing with "reactive" probes.

Mi Eun Jun1, Basab Roy, Kyo Han Ahn.   

Abstract

Chemical probes are valuable tools for the investigation of biochemical processes, diagnosis of disease markers, detection of hazardous compounds, and other purposes. Therefore, the development of chemical probes continues to grow through various approaches with different disciplines and design strategies. Fluorescent probes have received much attention because they are sensitive and easy-to-operate, in general. To realize desired selectivity toward a given analyte, the recognition site of a fluorescent probe is designed in such a way to maximize the binding interactions, usually through weak molecular forces such as hydrogen bonding, toward the analyte over other competing ones. In addition to such a supramolecular approach, the development of fluorescent probes that sense analytes through chemical reactions has witnessed its usefulness for achieving high selectivity, in many cases, superior to that obtainable by the supramolecular approach. Creative incorporations of the reactive groups to latent fluorophores have provided novel chemical probes for various analytes. In this feature article, we overview the recent progress in the development of turn-on fluorescent probes that are operating through chemical reactions triggered by target analytes. Various chemical reactions have been implemented in the development of many reactive probes with very high selectivity and sensitivity toward target analytes. A major emphasis has been focused on the type of chemical reactions utilized, with the hope that further explorations can be made with new chemical reactions to develop reactive probes useful for various applications.

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Year:  2011        PMID: 21552586     DOI: 10.1039/c1cc00014d

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  29 in total

1.  Fluorogenic diazaborine formation of semicarbazide with designed coumarin derivatives.

Authors:  Samantha Cambray; Anupam Bandyopadhyay; Jianmin Gao
Journal:  Chem Commun (Camb)       Date:  2017-11-21       Impact factor: 6.222

2.  A Ratiometric and near-Infrared Fluorescent Probe for Imaging Cu2+ in Living Cells and Animals.

Authors:  Rui Guo; Qiuan Wang; Weiying Lin
Journal:  J Fluoresc       Date:  2017-04-19       Impact factor: 2.217

3.  Reaction-based fluorescent sensor for investigating mobile Zn2+ in mitochondria of healthy versus cancerous prostate cells.

Authors:  Wen Chyan; Daniel Y Zhang; Stephen J Lippard; Robert J Radford
Journal:  Proc Natl Acad Sci U S A       Date:  2013-12-12       Impact factor: 11.205

4.  A Coumarin-Based Luminescent Chemosensor for Recognition of Cu2+ and its In-Situ Complex for CN- Sensing via Cu2+ Displacement Approach.

Authors:  Soma Mukherjee; Shrabani Talukder
Journal:  J Fluoresc       Date:  2016-11-22       Impact factor: 2.217

5.  A deep cavitand with a fluorescent wall functions as an ion sensor.

Authors:  Orion B Berryman; Aaron C Sather; Julius Rebek
Journal:  Org Lett       Date:  2011-09-13       Impact factor: 6.005

6.  Thiophene Appended Dual Fluorescent Sensor for Detection of Hg2+ and Cysteamine.

Authors:  Soma Sarkar; Swapnadip Roy; R N Saha; Sujit S Panja
Journal:  J Fluoresc       Date:  2017-12-28       Impact factor: 2.217

Review 7.  Boronate-based fluorescent probes: imaging hydrogen peroxide in living systems.

Authors:  Vivian S Lin; Bryan C Dickinson; Christopher J Chang
Journal:  Methods Enzymol       Date:  2013       Impact factor: 1.600

8.  A fluorescent indicator for imaging lysosomal zinc(II) with Förster resonance energy transfer (FRET)-enhanced photostability and a narrow band of emission.

Authors:  Kesavapillai Sreenath; Zhao Yuan; John R Allen; Michael W Davidson; Lei Zhu
Journal:  Chemistry       Date:  2014-11-07       Impact factor: 5.236

Review 9.  Covalent labeling of nucleic acids.

Authors:  Nils Klöcker; Florian P Weissenboeck; Andrea Rentmeister
Journal:  Chem Soc Rev       Date:  2020-10-21       Impact factor: 54.564

10.  Tricolor emission of a fluorescent heteroditopic ligand over a concentration gradient of zinc(II) ions.

Authors:  Kesavapillai Sreenath; Ronald J Clark; Lei Zhu
Journal:  J Org Chem       Date:  2012-09-05       Impact factor: 4.354

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