Discovery of Selective Ligands for Telomeric RNA G-quadruplexes (TERRA) through 19F-NMR Based Fragment Screening

被引:53
作者
Garavis, Miguel [1 ,6 ]
Lopez-Mendez, Blanca [2 ,3 ]
Somoza, Alvaro [4 ,5 ]
Oyarzabal, Julen [2 ,3 ]
Dalvit, Claudio [2 ,3 ]
Villasante, Alfredo [6 ]
Campos-Olivas, Ramon [2 ,3 ]
Gonzalez, Carlos [1 ]
机构
[1] CSIC, Inst Quim Fis Rocasolano, E-28006 Madrid, Spain
[2] Spanish Natl Canc Res Ctr CNIO, Spect & NMR Unit, Madrid 28029, Spain
[3] Spanish Natl Canc Res Ctr CNIO, Expt Therapeut Programme, Madrid 28029, Spain
[4] IMDEA Nanociencia, Madrid 28049, Spain
[5] CNB CSIC IMDEA Nanociencia Associated Unit Unidad, Madrid 28049, Spain
[6] Univ Autonoma Madrid, Ctr Biol Mol Severo Ochoa CSIC UAM, E-28049 Madrid, Spain
关键词
REPEAT-CONTAINING RNA; DRUG DISCOVERY; NMR-SPECTROSCOPY; HUMAN-CELLS; DNA; IDENTIFICATION; PARALLEL; BINDERS; LIBRARY; BINDING;
D O I
10.1021/cb500100z
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
Telomeric repeat-containing RNA (TERRA) is a novel and very attractive antitumoral target. Here, we report the first successful application of F-19-NMR fragment-based screening to identify chemically diverse compounds that bind to an RNA molecule such as TERRA. We have built a library of 355 fluorinated fragments, and checked their interaction with a long telomeric RNA as a target molecule. The screening resulted in the identification of 20 hits (hit rate of 5.6%). For a number of binders, their interaction with TERRA was confirmed by F-19- and H-1 NMR as well as by CD melting experiments. We have also explored the selectivity of the ligands for RNA G-quadruplexes and found that some of the hits do not interact with other nucleic acids such as tRNA and duplex DNA and, most importantly, favor the propeller-like parallel conformation in telomeric DNA G-quadruplexes. This suggests a selective recognition of this particular quadruplex topology and that different ligands may recognize specific sites in propeller-like parallel G-quadruplexes. Such features make some of the resulting binders promising lead compounds for fragment based drug discovery.
引用
收藏
页码:1559 / 1566
页数:8
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