Literature DB >> 29148442

Azadioxatriangulenium: a long fluorescence lifetime fluorophore for large biomolecule binding assay.

Thomas Just Sørensen1, Erling Thyrhaug, Mariusz Szabelski, Rafal Luchowski, Ignacy Gryczynski, Zygmunt Gryczynski, Bo W Laursen.   

Abstract

Of the many optical bioassays available, sensing by fluorescence anisotropy has great advantages as it provides a sensitive, instrumentally simple, ratiometric method of detection. However, it is hampered by a severe limitation, as the emission lifetime of the label needs to be comparable to the correlation lifetime (tumbling time) of the biomolecule which is labelled. For proteins of moderate size this is on the order of 20-200 ns, which due to practical issues currently limits the choice of labels to the dansyl-type dyes and certain aromatic dyes. These have the significant drawback of UV/blue absorption and emission as well as an often significant solvent sensitivity. Here, we report the synthesis and characterization of a new fluorescent label for high molecular weight biomolecule assay based on the azadioxatriangulenium motif. The NHS ester of the long fluorescence lifetime, red-emitting fluorophore: azadioxatriangulenium (ADOTA-NHS) was conjugated to anti-rabbit Immunoglobulin G (antiIgG). The long fluorescence lifetime was exploited to determine the correlation time of the high molecular weight antibody and its complex with rabbit Immunoglobulin G (IgG) with steady-state fluorescence anisotropy and time-resolved methods: solution phase immuno-assay was performed following either steady-state or time-resolved fluorescence anisotropy. By performing a variable temperature experiment it was determined that the binding of the ligand resulted in an increase in correlation time of more than 75%, and an increase in the steady-state anisotropy of 18%. The results show that the triangulenium class of dyes can be used in anisotropy assay to detect binding events involving biomolecules of far larger size than what is possible with most other red-emitting organic dyes.

Entities:  

Year:  2013        PMID: 29148442     DOI: 10.1088/2050-6120/1/2/025001

Source DB:  PubMed          Journal:  Methods Appl Fluoresc        ISSN: 2050-6120            Impact factor:   3.009


  6 in total

1.  Universal guidelines for the conversion of proteins and dyes into functional nanothermometers.

Authors:  Graham Spicer; Alejo Efeyan; Alejandro P Adam; Sebastian A Thompson
Journal:  J Biophotonics       Date:  2019-05-30       Impact factor: 3.207

2.  Design, synthesis, and time-gated cell imaging of carbon-bridged triangulenium dyes with long fluorescence lifetime and red emission.

Authors:  M Rosenberg; K R Rostgaard; Z Liao; A Ø Madsen; K L Martinez; T Vosch; B W Laursen
Journal:  Chem Sci       Date:  2018-02-23       Impact factor: 9.825

3.  Synthesis and properties of sulfur-functionalized triarylmethylium, acridinium and triangulenium dyes.

Authors:  Marco Santella; Eduardo Della Pia; Jakob Kryger Sørensen; Bo W Laursen
Journal:  Beilstein J Org Chem       Date:  2019-09-09       Impact factor: 2.883

4.  A fluorescent calix[4]arene with naphthalene units at the upper rim exhibits long fluorescence emission lifetime without fluorescence quenching.

Authors:  Masaki Takahashi; Naoya Tsuji; Kohei Yazaki; Yoshihisa Sei; Makoto Obata
Journal:  RSC Adv       Date:  2021-03-22       Impact factor: 3.361

5.  Long-lived bright red emitting azaoxa-triangulenium fluorophores.

Authors:  Badri P Maliwal; Rafal Fudala; Sangram Raut; Rutika Kokate; Thomas J Sørensen; Bo W Laursen; Zygmunt Gryczynski; Ignacy Gryczynski
Journal:  PLoS One       Date:  2013-05-07       Impact factor: 3.240

6.  C-Functionalized Cationic Diazaoxatriangulenes: Late-Stage Synthesis and Tuning of Physicochemical Properties.

Authors:  Irene Hernández Delgado; Simon Pascal; Céline Besnard; Silvia Voci; Laurent Bouffier; Neso Sojic; Jérôme Lacour
Journal:  Chemistry       Date:  2018-04-26       Impact factor: 5.236

  6 in total

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