Literature DB >> 24105107

Fluorogenic small molecules requiring reaction with a specific protein to create a fluorescent conjugate for biological imaging--what we know and what we need to learn.

Aleksandra Baranczak1, Stephen Connelly, Yu Liu, Sungwook Choi, Neil P Grimster, Evan T Powers, Ian A Wilson, Jeffery W Kelly.   

Abstract

We seek fluorogenic small molecules that generate a fluorescent conjugate signal if and only if they react with a given protein-of-interest (i.e., small molecules for which noncovalent binding to the protein-of-interest is insufficient to generate fluorescence). Consequently, it is the new chemical entity afforded by the generally irreversible reaction between the small molecule and the protein-of-interest that enables the energy of an electron occupying the lowest unoccupied molecular orbital (LUMO) of the chromophore to be given off as a photon instead of being dissipated by nonradiative mechanisms in complex biological environments. This category of fluorogenic small molecules is created by starting with environmentally sensitive fluorophores that are modified by an essential functional group that efficiently quenches the fluorescence until a chemoselective reaction between that functional group and the protein-of-interest occurs, yielding the fluorescent conjugate. Fluorogenic small molecules are envisioned to be useful for a wide variety of applications, including live cell imaging without the requirement for washing steps and pulse-chase kinetic analyses of protein synthesis, trafficking, degradation, etc.
Copyright © 2013 Wiley Periodicals, Inc.

Entities:  

Keywords:  environmentally sensitive fluorophores; fluorescence switching; reaction regulated quenching functional groups

Mesh:

Substances:

Year:  2014        PMID: 24105107      PMCID: PMC4128284          DOI: 10.1002/bip.22407

Source DB:  PubMed          Journal:  Biopolymers        ISSN: 0006-3525            Impact factor:   2.505


  69 in total

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2.  A stilbene that binds selectively to transthyretin in cells and remains dark until it undergoes a chemoselective reaction to create a bright blue fluorescent conjugate.

Authors:  Sungwook Choi; Derrick Sek Tong Ong; Jeffery W Kelly
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3.  A photoactivatable push-pull fluorophore for single-molecule imaging in live cells.

Authors:  Samuel J Lord; Nicholas R Conley; Hsiao-lu D Lee; Reichel Samuel; Na Liu; Robert J Twieg; W E Moerner
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4.  Dimer formation from 1-amino-8-naphthalenesulfonate catalyzed by bovine serum albumin. A new fluorescent molecule with exceptional binding properties.

Authors:  C G Rosen; G Weber
Journal:  Biochemistry       Date:  1969-10       Impact factor: 3.162

5.  Structure of a complex of two plasma proteins: transthyretin and retinol-binding protein.

Authors:  H L Monaco; M Rizzi; A Coda
Journal:  Science       Date:  1995-05-19       Impact factor: 47.728

6.  No-wash protein labeling with designed fluorogenic probes and application to real-time pulse-chase analysis.

Authors:  Shin Mizukami; Shuji Watanabe; Yuri Akimoto; Kazuya Kikuchi
Journal:  J Am Chem Soc       Date:  2012-01-06       Impact factor: 15.419

7.  Fluorescence of buried tyrosine residues in proteins.

Authors:  V Giancotti; F Quadrifoglio; R W Cowgill; C Crane-Robinson
Journal:  Biochim Biophys Acta       Date:  1980-07-24

8.  Enzymatic activation of nitro-aryl fluorogens in live bacterial cells for enzymatic turnover-activated localization microscopy†

Authors:  Marissa K Lee; Jarrod Williams; Robert J Twieg; Jianghong Rao; W E Moerner
Journal:  Chem Sci       Date:  2013       Impact factor: 9.825

Review 9.  DCDHF fluorophores for single-molecule imaging in cells.

Authors:  Samuel J Lord; Nicholas R Conley; Hsiao-Lu D Lee; Stefanie Y Nishimura; Andrea K Pomerantz; Katherine A Willets; Zhikuan Lu; Hui Wang; Na Liu; Reichel Samuel; Ryan Weber; Alexander Semyonov; Meng He; Robert J Twieg; W E Moerner
Journal:  Chemphyschem       Date:  2009-01-12       Impact factor: 3.102

10.  Development of SNAP-tag fluorogenic probes for wash-free fluorescence imaging.

Authors:  Xiaoli Sun; Aihua Zhang; Brenda Baker; Luo Sun; Angela Howard; John Buswell; Damien Maurel; Anastasiya Masharina; Kai Johnsson; Christopher J Noren; Ming-Qun Xu; Ivan R Corrêa
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  4 in total

1.  A fluorogenic aryl fluorosulfate for intraorganellar transthyretin imaging in living cells and in Caenorhabditis elegans.

Authors:  Aleksandra Baranczak; Yu Liu; Stephen Connelly; Wen-Ge Han Du; Erin R Greiner; Joseph C Genereux; R Luke Wiseman; Yvonne S Eisele; Nadine C Bradbury; Jiajia Dong; Louis Noodleman; K Barry Sharpless; Ian A Wilson; Sandra E Encalada; Jeffery W Kelly
Journal:  J Am Chem Soc       Date:  2015-06-08       Impact factor: 15.419

2.  Stilbene vinyl sulfonamides as fluorogenic sensors of and traceless covalent kinetic stabilizers of transthyretin that prevent amyloidogenesis.

Authors:  Eul Hyun Suh; Yu Liu; Stephen Connelly; Joseph C Genereux; Ian A Wilson; Jeffery W Kelly
Journal:  J Am Chem Soc       Date:  2013-11-18       Impact factor: 15.419

3.  Sulfonyl fluorides as privileged warheads in chemical biology.

Authors:  Arjun Narayanan; Lyn H Jones
Journal:  Chem Sci       Date:  2015-03-16       Impact factor: 9.825

4.  Fluorescence Turn-On Folding Sensor To Monitor Proteome Stress in Live Cells.

Authors:  Yu Liu; Xin Zhang; Wentao Chen; Yun Lei Tan; Jeffery W Kelly
Journal:  J Am Chem Soc       Date:  2015-08-25       Impact factor: 15.419

  4 in total

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