Literature DB >> 24338798

Polar red-emitting rhodamine dyes with reactive groups: synthesis, photophysical properties, and two-color STED nanoscopy applications.

Kirill Kolmakov1, Christian A Wurm, Dirk N H Meineke, Fabian Göttfert, Vadim P Boyarskiy, Vladimir N Belov, Stefan W Hell.   

Abstract

The synthesis, reactivity, and photophysical properties of new rhodamines with intense red fluorescence, two polar residues (hydroxyls, primary phosphates, or sulfonic acid groups), and improved hydrolytic stability of the amino-reactive sites (NHS esters or mixed N-succinimidyl carbonates) are reported. All fluorophores contain an N-alkyl-1,2-dihydro-2,2,4-trimethylquinoline fragment, and most of them bear a fully substituted tetrafluoro phenyl ring with a secondary carboxamide group. The absorption and emission maxima in water are in the range of 635-639 and 655-659 nm, respectively. A vastly simplified approach to red-emitting rhodamines with two phosphate groups that are compatible with diverse functional linkers was developed. As an example, a phosphorylated dye with an azide residue was prepared and was used in a click reaction with a strained alkyne bearing an N-hydroxysuccinimid (NHS) ester group. This method bypasses the undesired activation of phosphate groups, and gives an amphiphilic amino-reactive dye, the solubility and distribution of which between aqueous and organic phases can be controlled by varying the pH. The presence of two hydroxyl groups and a phenyl ring with two carboxyl residues in the dyes with another substitution pattern is sufficient for providing the hydrophilic properties. Selective formation of a mono-N-hydroxysuccinimidyl ester from 5-carboxy isomer of this rhodamine is reported. The fluorescence quantum yields varied from 58 to 92% for free fluorophores, and amounted to 18-64% for antibody conjugates in aqueous buffers. The brightness and photostability of these fluorophores facilitated two-color stimulated emission depletion (STED) fluorescence nanoscopy of biological samples with high contrast and minimal background. Selecting a pair of fluorophores with absorption/emission bands at 579/609 and 635/655 nm enabled two-color channels with low cross-talk and negligible background at approximately 40 nm resolution.
Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  bioconjugation; chromophores; click chemistry; fluorescent probes; rhodamines

Mesh:

Substances:

Year:  2013        PMID: 24338798     DOI: 10.1002/chem.201303433

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


  11 in total

1.  Gated STED microscopy with time-gated single-photon avalanche diode.

Authors:  Iván Coto Hernández; Mauro Buttafava; Gianluca Boso; Alberto Diaspro; Alberto Tosi; Giuseppe Vicidomini
Journal:  Biomed Opt Express       Date:  2015-05-27       Impact factor: 3.732

2.  Red Emitting Coumarins: Insights of Photophysical Properties with DFT Methods.

Authors:  Abhinav B Tathe; Lydia Rhyman; Ponnadurai Ramasami; Nagaiyan Sekar
Journal:  J Fluoresc       Date:  2015-07-03       Impact factor: 2.217

3.  A photostable fluorescent marker for the superresolution live imaging of the dynamic structure of the mitochondrial cristae.

Authors:  Chenguang Wang; Masayasu Taki; Yoshikatsu Sato; Yasushi Tamura; Hideyuki Yaginuma; Yasushi Okada; Shigehiro Yamaguchi
Journal:  Proc Natl Acad Sci U S A       Date:  2019-07-23       Impact factor: 11.205

4.  NLOphoric Red Emitting Bis Coumarins with O-BF(2)-O core - Synthesis, Photophysical Properties and DFT Studies.

Authors:  Abhinav B Tathe; Nagaiyan Sekar
Journal:  J Fluoresc       Date:  2015-12-11       Impact factor: 2.217

5.  In Situ Visualization of Block Copolymer Self-Assembly in Organic Media by Super-Resolution Fluorescence Microscopy.

Authors:  Charlotte E Boott; Romain F Laine; Pierre Mahou; John R Finnegan; Erin M Leitao; Stephen E D Webb; Clemens F Kaminski; Ian Manners
Journal:  Chemistry       Date:  2015-11-10       Impact factor: 5.236

6.  Mirror-enhanced super-resolution microscopy.

Authors:  Xusan Yang; Hao Xie; Eric Alonas; Yujia Liu; Xuanze Chen; Philip J Santangelo; Qiushi Ren; Peng Xi; Dayong Jin
Journal:  Light Sci Appl       Date:  2016-06-17       Impact factor: 17.782

7.  Precision targeted ruthenium(ii) luminophores; highly effective probes for cell imaging by stimulated emission depletion (STED) microscopy.

Authors:  Aisling Byrne; Christopher S Burke; Tia E Keyes
Journal:  Chem Sci       Date:  2016-06-30       Impact factor: 9.825

Review 8.  Navigating challenges in the application of superresolution microscopy.

Authors:  Talley J Lambert; Jennifer C Waters
Journal:  J Cell Biol       Date:  2016-12-05       Impact factor: 10.539

9.  High-Affinity Functional Fluorescent Ligands for Human β-Adrenoceptors.

Authors:  Gyuzel Y Mitronova; Gražvydas Lukinavičius; Alexey N Butkevich; Tobias Kohl; Vladimir N Belov; Stephan E Lehnart; Stefan W Hell
Journal:  Sci Rep       Date:  2017-09-26       Impact factor: 4.379

10.  Fluorescent Rhodamines and Fluorogenic Carbopyronines for Super-Resolution STED Microscopy in Living Cells.

Authors:  Alexey N Butkevich; Gyuzel Yu Mitronova; Sven C Sidenstein; Jessica L Klocke; Dirk Kamin; Dirk N H Meineke; Elisa D'Este; Philip-Tobias Kraemer; Johann G Danzl; Vladimir N Belov; Stefan W Hell
Journal:  Angew Chem Int Ed Engl       Date:  2016-02-04       Impact factor: 15.336

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