A versatile nanomachine for the sensitive detection of platelet-derived growth factor-BB utilizing a G-quadruplex-selective iridium(III) complex

被引:39
作者
Lu, Lihua [1 ,2 ]
Mao, Zhifeng [2 ]
Kang, Tian-Shu [3 ]
Leung, Chung-Hang [3 ]
Ma, Dik-Lung [2 ]
机构
[1] Qingdao Agr Univ, Coll Chem & Pharmaceut Sci, Qingdao 266109, Peoples R China
[2] Hong Kong Baptist Univ, Dept Chem, Kowloon Tong, Hong Kong, Peoples R China
[3] Univ Macau, Inst Chinese Med Sci, State Key Lab Qual Res Chinese Med, Macau, Peoples R China
基金
中国国家自然科学基金;
关键词
G-quadruplex; Iridium(III) complex; Nanomachine; PDGF-BB; Luminescent; ROLLING CIRCLE AMPLIFICATION; STRAND-DISPLACEMENT AMPLIFICATION; CHAIN-REACTION PCR; LABEL-FREE; MICRORNA DETECTION; ELECTROCHEMICAL DETECTION; SIGNAL AMPLIFICATION; DNA MACHINE; ENZYME-FREE; APTAMER;
D O I
10.1016/j.bios.2016.05.026
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The novel iridium(III) complex 1 was found to be highly selective for G-quadruplex DNA, and was employed for the development of a versatile nanomachine. In the nanomachine, the single-stranded DNA (ssDNA) oligonucleotide ON1 hybridizes with the hairpin DNA oligonucleotide ON2, leading to the formation of a 5'-recessed double-stranded DNA (dsDNA) structure and the simultaneous release of a G-rich DNA sequence, which folds into a G-quadruplex motif that is recognized by complex 1. Upon the addition of Exo III, the dsDNA substrate is digested leading to the liberation of ON1 ssDNA, which enters a new cycle of the nanomachine. This nanomachine was successfully used to detect PDGF-BB by combination with a simple pre-procedure module, and exhibited a linear response between luminescence intensity and PDGF-BB concentration in the range of 10 to 300 pM (R-2 = 0.992), with a limit of detection for PDGF-BB of 10 pM. This assay was highly selective for PDGF-BB over other proteins, and exhibited potential use in biological sample analysis. Moreover, the versatility of the nanomachine was demonstrated by adapting the nanomachine for the detection of thrombin by simply changing the pre-procedure module. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:300 / 309
页数:10
相关论文
共 69 条
  • [1] ABSOLUTE MESSENGER-RNA QUANTIFICATION USING THE POLYMERASE CHAIN-REACTION (PCR) - A NOVEL-APPROACH BY A PCR AIDED TRANSCRIPT TITRATION ASSAY (PATTY)
    BECKERANDRE, M
    HAHLBROCK, K
    [J]. NUCLEIC ACIDS RESEARCH, 1989, 17 (22) : 9437 - 9446
  • [2] Label-free chemiluminescent aptasensor for platelet-derived growth factor detection based on exonuclease-assisted cascade autocatalytic recycling amplification
    Bi, Sai
    Luo, Baoyu
    Ye, Jiayan
    Wang, Zonghua
    [J]. BIOSENSORS & BIOELECTRONICS, 2014, 62 : 208 - 213
  • [3] Detection of sequence-specific protein-DNA interactions via surface enhanced resonance Raman scattering
    Bonham, Andrew J.
    Braun, Gary
    Pavel, Ioana
    Moskovits, Martin
    Reich, Norbert O.
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (47) : 14572 - +
  • [4] Aptamer-based colorimetric detection of platelet-derived growth factor using unmodified gold nanoparticles
    Chang, Chia-Chen
    Wei, Shih-Chung
    Wu, Tzu-Heng
    Lee, Chung-Han
    Lin, Chii-Wann
    [J]. BIOSENSORS & BIOELECTRONICS, 2013, 42 : 119 - 123
  • [5] Signal-off Electrochemiluminescence Biosensor Based on Phi29 DNA Polymerase Mediated Strand Displacement Amplification for MicroRNA Detection
    Chen, Anyi
    Gui, Guo-Feng
    Zhuo, Ying
    Chai, Ya-Qin
    Xiang, Yun
    Yuan, Ruo
    [J]. ANALYTICAL CHEMISTRY, 2015, 87 (12) : 6328 - 6334
  • [6] Phosphorescent iridium(III) complexes as multicolor probes for specific mitochondrial imaging and tracking
    Chen, Yu
    Qiao, Liping
    Ji, Liangnian
    Chao, Hui
    [J]. BIOMATERIALS, 2014, 35 (01) : 2 - 13
  • [7] The application of DNA and RNA G-quadruplexes to therapeutic medicines
    Collie, Gavin W.
    Parkinson, Gary N.
    [J]. CHEMICAL SOCIETY REVIEWS, 2011, 40 (12) : 5867 - 5892
  • [8] Fluorescence-based melting assays for studying quadruplex ligands
    De Cian, Anne
    Guittat, Lionel
    Kaiser, Markus
    Sacca, Barbara
    Amrane, Samir
    Bourdoncle, Anne
    Alberti, Patrizia
    Teulade-Fichou, Marie-Paule
    Lacroix, Laurent
    Mergny, Jean-Louis
    [J]. METHODS, 2007, 42 (02) : 183 - 195
  • [9] de la Faverie A. R., 2014, NUCLEIC ACIDS RES, V42, P376
  • [10] Sensitivity and accuracy of quantitative real-time polymerase chain reaction using SYBR green I depends on cDNA synthesis conditions
    Deprez, RHL
    Fijnvandraat, AC
    Ruijter, JM
    Moorman, AFM
    [J]. ANALYTICAL BIOCHEMISTRY, 2002, 307 (01) : 63 - 69