Literature DB >> 25695375

Discovery, understanding, and bioapplication of organic fluorophore: a case study with an indolizine-based novel fluorophore, Seoul-Fluor.

Eunha Kim1, Youngjun Lee2, Sanghee Lee2, Seung Bum Park2.   

Abstract

Owing to its high sensitivity and great applicability, the fluorescence phenomenon has been considered as an inevitable research tool in the modern scientific fields of chemistry, biology, materials science, biomedical science, and their interfaces. Many strategies have been pursued to understand and manipulate the photophysical properties of fluorescent materials, but the scientific community has been focused on the repeated application of existing organic fluorophores or the identification of unique fluorescence properties in a trial-and-error basis without systematic studies. Moreover, recent studies are emphasizing the necessity of deeper understanding about the structure-photophysical property relationship of organic fluorophores for the development of better fluorescent probes. Herein, we provide an overview of a novel fluorescent molecular framework, Seoul-Fluor, which can be rationally engineered to furnish a wide variety of fluorophores in terms of the photophysical properties. Seoul-Fluor is built on an indolizine-based fluorescent platform with three different positions to introduce various substituents: R(1) and R(2) substituents for electronic perturbation; R(3) substituent as a functional handle for bioconjugation. Over the past decade, we have demonstrated that the Seoul-Fluor system has (i) tunable and predictable emission wavelength covering a full visible-color range; (ii) controllable quantum yield via photoinduced electron transfer phenomenon; and (iii) environment-sensitive fluorogenic properties that can be modified through intramolecular charge transfer processes. We convincingly demonstrated the prediction of photophysical properties, that is, emission wavelength and quantum yield, through the construction of a systematic set of analogues and the subsequent analysis of their photophysical properties without the highly sophisticated theoretical support. Guided by quantifiable parameters such as the Hammett substituent constants or energy levels of the molecular orbitals, this unique organic fluorophore can serve as a versatile molecular platform for the development of novel fluorescent switchable biosensors and fluorogenic bioprobes. In this Account, we will discuss the discovery and recent progress made on Seoul-Fluor, the rational design of Seoul-Fluor-based bioprobes, and their practical applications to specific biological processes that are facilitated by systematic studies of the structure-photophysical property relationships.

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Year:  2015        PMID: 25695375     DOI: 10.1021/ar500370v

Source DB:  PubMed          Journal:  Acc Chem Res        ISSN: 0001-4842            Impact factor:   22.384


  23 in total

1.  A de novo strategy to develop NIR precipitating fluorochrome for long-term in situ cell membrane bioimaging.

Authors:  Ke Li; Yifan Lyu; Yan Huang; Shuai Xu; Hong-Wen Liu; Lanlan Chen; Tian-Bing Ren; Mengyi Xiong; Shuangyan Huan; Lin Yuan; Xiao-Bing Zhang; Weihong Tan
Journal:  Proc Natl Acad Sci U S A       Date:  2021-02-23       Impact factor: 11.205

2.  Intravital two-photon imaging and quantification of hepatic steatosis and fibrosis in a live small animal model.

Authors:  Jieun Moon; Jehwi Jeon; Eunji Kong; Sujung Hong; Jingu Lee; Eun Kyung Lee; Pilhan Kim
Journal:  Biomed Opt Express       Date:  2021-12-01       Impact factor: 3.732

3.  Ratiometric mechanosensitive fluorescent dyes: Design and applications.

Authors:  Mark A Haidekker; Emmanuel A Theodorakis
Journal:  J Mater Chem C Mater       Date:  2016-01-14       Impact factor: 7.393

4.  Diazaoxatriangulenium: synthesis of reactive derivatives and conjugation to bovine serum albumin.

Authors:  Ilkay Bora; Sidsel A Bogh; Martin Rosenberg; Marco Santella; Thomas Just Sørensen; Bo W Laursen
Journal:  Org Biomol Chem       Date:  2015-12-03       Impact factor: 3.876

5.  Kaleidoscopic fluorescent arrays for machine-learning-based point-of-care chemical sensing.

Authors:  Hyungi Kim; Sang-Kee Choi; Jungmo Ahn; Hojeong Yu; Kyoungha Min; Changgi Hong; Ik-Soo Shin; Sanghee Lee; Hakho Lee; Hyungsoon Im; JeongGil Ko; Eunha Kim
Journal:  Sens Actuators B Chem       Date:  2020-12-01       Impact factor: 7.460

Review 6.  Lessons in Organic Fluorescent Probe Discovery.

Authors:  Sachin B Wagh; Vladimir A Maslivetc; James J La Clair; Alexander Kornienko
Journal:  Chembiochem       Date:  2021-06-23       Impact factor: 3.164

7.  [3 + 2]-Annulation of pyridinium ylides with 1-chloro-2-nitrostyrenes unveils a tubulin polymerization inhibitor.

Authors:  Alexander V Aksenov; Nikolai A Arutiunov; Nikita K Kirilov; Dmitrii A Aksenov; Igor Yu Grishin; Nicolai A Aksenov; Huifen Wang; Liqin Du; Tania Betancourt; Stephen C Pelly; Alexander Kornienko; Michael Rubin
Journal:  Org Biomol Chem       Date:  2021-08-13       Impact factor: 3.890

8.  Functionalized quinolizinium-based fluorescent reagents for modification of cysteine-containing peptides and proteins.

Authors:  Karen Ka-Yan Kung; Cai-Fung Xu; Wa-Yi O; Qiong Yu; Sai-Fung Chung; Suet-Ying Tam; Yun-Chung Leung; Man-Kin Wong
Journal:  RSC Adv       Date:  2022-02-22       Impact factor: 3.361

Review 9.  Rational design of small molecule fluorescent probes for biological applications.

Authors:  Joomyung V Jun; David M Chenoweth; E James Petersson
Journal:  Org Biomol Chem       Date:  2020-08-05       Impact factor: 3.876

10.  Palladium catalyzed synthesis of indolizines via the carbonylative coupling of bromopyridines, imines and alkynes.

Authors:  Sébastien A Roy; José Zgheib; Cuihan Zhou; Bruce A Arndtsen
Journal:  Chem Sci       Date:  2020-12-22       Impact factor: 9.825

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