Ligands playing musical chairs with G-quadruplex DNA: A rapid and simple displacement assay for identifying selective G-quadruplex binders

被引:225
作者
Monchaud, D. [1 ]
Allain, C. [1 ]
Bertrand, H. [1 ]
Smargiasso, N. [2 ]
Rosu, F. [2 ]
Gabelica, V. [2 ]
De Cian, A. [3 ,4 ]
Mergny, J. -L. [3 ,4 ]
Teulade-Fichou, M. -R [1 ]
机构
[1] Ctr Univ Paris XI, CNRS, Inst Curie, Sect Rech,UMR176, F-91405 Orsay, France
[2] Univ Liege, Inst Chim, Lab Spectrometrie Masse, GIGA R, B-4000 Liege, Belgium
[3] Museum Natl Hist Nat, Acides Nucl Dynam Ciblage & Fonct Biol, INSERM, U565,USM 503, F-75005 Paris, France
[4] Museum Natl Hist Nat, Lab Regulat & Dynam Genome, CNRS, UMR5153,USM 503, F-75005 Paris, France
关键词
G-quadruplex DNA; thiazole orange; G-quadruplex ligands; fluorescent intercalator displacement;
D O I
10.1016/j.biochi.2008.02.019
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We report here the details of G4-FlD (G-quadruplex fluorescent intercalator displacement), a simple method aiming at evaluating quadruplex-DNA binding affinity and quadruplex-over duplex-DNA selectivity of putative ligands. This assay is based on the loss of fluorescence upon displacement of thiazole orange from quadruplex- and duplex-DNA matrices. The original protocol was tested using various quadruplex- and duplex-DNA targets, and with a wide panel of G-quadruplex ligands belonging to different families (i.e. from quinacridines to metallo-organic ligands) likely to display various binding modes. The reliability of the assay is further supported by comparisons with FRET-melting and ESI-MS assays. (C) 2008 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:1207 / 1223
页数:17
相关论文
共 73 条
[41]   Development of a fluorescent intercalator displacement assay (G4-FID) for establishing quadruplex-DNA affinity and selectivity of putative ligands [J].
Monchaud, David ;
Allain, Clemence ;
Teulade-Fichou, Marie-Paule .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2006, 16 (18) :4842-4845
[42]   Chemical approaches to the discovery and development of cancer therapies [J].
Neidle, S ;
Thurston, DE .
NATURE REVIEWS CANCER, 2005, 5 (04) :285-296
[43]  
Neidle S, 2006, RSC BIOMOL SCI, P1, DOI 10.1039/9781847555298
[44]   Telomere maintenance as a target for anticancer drug discovery [J].
Neidle, S ;
Parkinson, G .
NATURE REVIEWS DRUG DISCOVERY, 2002, 1 (05) :383-393
[45]   Biosensor-surface plasmon resonance: Quantitative analysis of small molecule-nucleic acid interactions [J].
Nguyen, Binh ;
Tanious, Farial A. ;
Wilson, W. David .
METHODS, 2007, 42 (02) :150-161
[46]  
Nygren J, 1998, BIOPOLYMERS, V46, P39, DOI 10.1002/(SICI)1097-0282(199807)46:1<39::AID-BIP4>3.0.CO
[47]  
2-Z
[48]   Physiological relevance of telomeric G-quadruplex formation: a potential drug target [J].
Oganesian, Liana ;
Bryan, Tracy M. .
BIOESSAYS, 2007, 29 (02) :155-165
[49]   Exogenous ligand binding property of a heme-DNA coordination complex [J].
Ohyama, T ;
Kato, Y ;
Mita, H ;
Yamamoto, Y .
CHEMISTRY LETTERS, 2006, 35 (01) :126-127
[50]   Energetics of quadruplex-drug recognition in anticancer therapy [J].
Pagano, Bruno ;
Giancola, Concetta .
CURRENT CANCER DRUG TARGETS, 2007, 7 (06) :520-540