Specific interactions with intra- and intermolecular G-quadruplex DNA structures by hydrosoluble coronene derivatives: A new class of telomerase inhibitors

被引:52
作者
Franceschin, Marco
Alvino, Antonello
Casagrande, Valentina
Mauriello, Clementina
Pascucci, Emanuela
Savino, Maria
Ortaggi, Giancarlo
Bianco, Armandodoriano
机构
[1] Univ Roma La Sapienza, Dipartimento Chim, I-00185 Rome, Italy
[2] Univ Roma La Sapienza, Dipartimento Genet & Biol Mol, I-00185 Rome, Italy
[3] Univ Roma La Sapienza, CNR, Ist Biol & Patol Mol, I-00185 Rome, Italy
[4] Univ Roma La Sapienza, CNR, Ist Chim Biomol, I-00185 Rome, Italy
关键词
hydrosoluble coronene derivatives; G-quadruplex; telomerase inhibitors;
D O I
10.1016/j.bmc.2006.11.032
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
In developing G-quadruplex interactive telomerase inhibitors two main features have to be taken into account: the hydrophobic interactions with the G-quartet plane and the electrostatic interactions with the negatively charged phosphates of the four grooves. In this paper, we report the synthesis of four hydrosoluble coronene derivatives, which are characterized by a large hydrophobic aromatic core and four orthogonal hydrophilic side chains. We have studied their ability to induce both inter- and intramolecular G-quadruplex structures and found a significant selectivity of all the coronene derivatives for the intramolecular G-quadruplex. The efficiency in inhibiting human telomerase has been evaluated in a cell-free system and the experimental results correlate with the relative affinities of these compounds for the G-quadruplex monomeric structure, as derived by molecular modelling simulations. Thus, the coronene derivatives can be considered as a new class of telomerase inhibitors, although further investigations are surely necessary to fully exploit their features. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1848 / 1858
页数:11
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