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State-of-the-art methodologies for the discovery and characterization of DNA G-quadruplex binders.

Authors :
Pagano B
Cosconati S
Gabelica V
Petraccone L
De Tito S
Marinelli L
La Pietra V
di Leva FS
Lauri I
Trotta R
Novellino E
Giancola C
Randazzo A
Source :
Current pharmaceutical design [Curr Pharm Des] 2012; Vol. 18 (14), pp. 1880-99.
Publication Year :
2012

Abstract

Nowadays, the molecular basis of interaction between low molecular weight compounds and biological macromolecules is the subject of numerous investigations aimed at the rational design of molecules with specific therapeutic applications. In the last decades, it has been demonstrated that DNA quadruplexes play a critical role in several biological processes both at telomeric and gene promoting levels thus providing a great stride in the discovery of ligands able to interact with such a biologically relevant DNA conformation. So far, a number of experimental and computational approaches have been successfully employed in order to identify new ligands and to characterize their binding to the DNA. The main focus of this review is the description of these methodologies, placing a particular emphasis on computational methods, isothermal titration calorimetry (ITC), mass spectrometry (MS), nuclear magnetic resonance (NMR), circular dichroism (CD) and fluorescence spectroscopies.

Details

Language :
English
ISSN :
1873-4286
Volume :
18
Issue :
14
Database :
MEDLINE
Journal :
Current pharmaceutical design
Publication Type :
Academic Journal
Accession number :
22376104
Full Text :
https://doi.org/10.2174/138161212799958332