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Molecules 2015, 20(1), 206-223; doi:10.3390/molecules20010206

Structure-Based Virtual Screening of Novel Natural Alkaloid Derivatives as Potential Binders of h-telo and c-myc DNA G-Quadruplex Conformations

1
Dipartimento di Scienze della Salute, Università degli Studi "Magna Græcia", Campus "S. Venuta", Viale Europa, Germaneto 88100, Catanzaro, Italy
2
Dipartimento di Scienze della Vita e dell'Ambiente, Università degli Studi di Cagliari, Via Ospedale 72, Cagliari 09124, Italy
These authors contributed equally to this work.
*
Author to whom correspondence should be addressed.
Academic Editors: Patricia Valentao and Mariana Sottomayor
Received: 7 November 2014 / Accepted: 15 December 2014 / Published: 24 December 2014
(This article belongs to the Special Issue Alkaloids: Novel Therapeutic Perspectives)
View Full-Text   |   Download PDF [2183 KB, uploaded 24 December 2014]   |  

Abstract

Several ligands can bind to the non-canonical G-quadruplex DNA structures thereby stabilizing them. These molecules can act as effective anticancer agents by stabilizing the telomeric regions of DNA or by regulating oncogene expression. In order to better interact with the quartets of G-quadruplex structures, G-binders are generally characterized by a large aromatic core involved in π-π stacking. Some natural flexible cyclic molecules from Traditional Chinese Medicine have shown high binding affinity with G-quadruplex, such as berbamine and many other alkaloids. Using the structural information available on G-quadruplex structures, we performed a high throughput in silico screening of commercially available alkaloid derivative databases by means of a structure-based approach based on docking and molecular dynamics simulations against the human telomeric sequence d[AG3(T2AG3)3] and the c-myc promoter structure. We identified 69 best hits reporting an improved theoretical binding affinity with respect to the active set. Among them, a berberine derivative, already known to remarkably inhibit telomerase activity, was related to a better theoretical affinity versus c-myc. View Full-Text
Keywords: DNA; G-quadruplex; h-telo; c-myc; alkaloids; berberine; virtual screening; docking; molecular dynamics DNA; G-quadruplex; h-telo; c-myc; alkaloids; berberine; virtual screening; docking; molecular dynamics
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This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. (CC BY 4.0).

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MDPI and ACS Style

Rocca, R.; Moraca, F.; Costa, G.; Alcaro, S.; Distinto, S.; Maccioni, E.; Ortuso, F.; Artese, A.; Parrotta, L. Structure-Based Virtual Screening of Novel Natural Alkaloid Derivatives as Potential Binders of h-telo and c-myc DNA G-Quadruplex Conformations. Molecules 2015, 20, 206-223.

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