Thioflavin T as a fluorescence probe for biosensing applications

被引:97
作者
Khusbu, Farjana Yeasmin [1 ]
Zhou, Xi [1 ]
Chen, Hanchun [1 ]
Ma, Changbei [1 ]
Wang, Kemin [2 ]
机构
[1] Cent S Univ, Sch Life Sci, Changsha 410013, Hunan, Peoples R China
[2] Hunan Univ, State Key Lab Chemo Biosensing & Chemometr, Changsha 410081, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
Thioflavin T; Sensor; Fluorescence; G-quadruplex; Label-free; TARGETING TRANSCRIPTION FACTORS; ROLLING CIRCLE AMPLIFICATION; DNA GLYCOSYLASE ACTIVITY; HELIX MOLECULAR SWITCH; LABEL-FREE DETECTION; TURN-ON DETECTION; G-QUADRUPLEX; SENSITIVE DETECTION; ENZYME-FREE; ULTRASENSITIVE DETECTION;
D O I
10.1016/j.trac.2018.09.013
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Thioflavin T (ThT), a water-soluble fluorescence probe and the conventional dye for the detection of amyloid fibrils has recently been demonstrated to recognize and bind nucleic acids. It induces the formation of G-quadruplex (G4) structure and appears as a sensor by emitting enhanced fluorescence. Incorporation of G-rich sequences in the nucleic acid amplification procedures assists the observation of the final products. In this manner, ThT with the "light-up" nature has emerged as a well-liked dye being devised in several biosensing applications. It offers sensitive and straightforward detection of bio-substrates including nucleic acids, proteins, small molecules as well as measurement of enzyme activities with the advantages of specificity, reduced background signal, and minimal cost. In this review, we aim to present a thorough overview of the ThT-based biosensing applications along with ThT/G-quadruplex complex formation and ThT-associated amplification techniques. (c) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 18
页数:18
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共 114 条
  • [1] Rolling circle amplification: a versatile tool for chemical biology, materials science and medicine
    Ali, M. Monsur
    Li, Feng
    Zhang, Zhiqing
    Zhang, Kaixiang
    Kang, Dong-Ku
    Ankrum, James A.
    Le, X. Chris
    Zhao, Weian
    [J]. CHEMICAL SOCIETY REVIEWS, 2014, 43 (10) : 3324 - 3341
  • [2] Molecular Rotors: What Lies Behind the High Sensitivity of the Thioflavin-T Fluorescent Marker
    Amdursky, Nadav
    Erez, Yuval
    Huppert, Dan
    [J]. ACCOUNTS OF CHEMICAL RESEARCH, 2012, 45 (09) : 1548 - 1557
  • [3] A Potassium Ion-Dependent RNA Structural Switch Regulates Human Pre-miRNA 92b Maturation
    Arachchilage, Gayan Mirihana
    Dassanayake, Arosha C.
    Basu, Soumitra
    [J]. CHEMISTRY & BIOLOGY, 2015, 22 (02): : 262 - 272
  • [4] Binding of berberine to human telomeric quadruplex - spectroscopic, calorimetric and molecular modeling studies
    Arora, Amit
    Balasubramanian, Chandramouli
    Kumar, Niti
    Agrawal, Saurabh
    Ojha, Rajendra P.
    Maiti, Souvik
    [J]. FEBS JOURNAL, 2008, 275 (15) : 3971 - 3983
  • [5] Fluorescent dyes specific for quadruplex DNA
    Arthanari, H
    Basu, S
    Kawano, TL
    Bolton, PH
    [J]. NUCLEIC ACIDS RESEARCH, 1998, 26 (16) : 3724 - 3728
  • [6] A rapid biosensor for highly sensitive protein detection based on G-quadruplex-Thioflavin T complex and terminal protection of small molecule-linked DNA
    Bai, Dongmei
    Ji, Danyang
    Shang, Jinhua
    Hu, Yalei
    Gao, Jia
    Lin, Zhang
    Ge, Jia
    Li, Zhaohui
    [J]. SENSORS AND ACTUATORS B-CHEMICAL, 2017, 252 : 1146 - 1152
  • [7] Targeting G-quadruplexes in gene promoters: a novel anticancer strategy?
    Balasubramanian, Shankar
    Hurley, Laurence H.
    Neidle, Stephen
    [J]. NATURE REVIEWS DRUG DISCOVERY, 2011, 10 (04) : 261 - 275
  • [8] Interaction of malachite green with guanine-rich single-stranded DNA: preferential binding to a G-quadruplex
    Bhasikuttan, Achikanath C.
    Mohanty, Jyotirmayee
    Pal, Haridas
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2007, 46 (48) : 9305 - 9307
  • [9] Molecular mechanism of Thioflavin-T binding to amyloid fibrils
    Biancalana, Matthew
    Koide, Shohei
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS, 2010, 1804 (07): : 1405 - 1412
  • [10] Mechanistic aspects of thioflavin-T self-aggregation and DNA binding: evidence for dimer attack on DNA grooves
    Biancardi, A.
    Biver, T.
    Burgalassi, A.
    Mattonai, M.
    Secco, F.
    Venturini, M.
    [J]. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2014, 16 (37) : 20061 - 20072