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Nucleic Acids Symposium Series 2007 51(1):39-40; doi:10.1093/nass/nrm020
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© 2007 Oxford University Press

The impact of 8-aryl-and 8-heteroaryl-2'-deoxyguanosine derivatives on G-quadruplex formation

Vladimir Gubala, María del C. Rivera-Sánchez, Gerard Hobley and José M. Rivera*

Department of Chemistry, University of Puerto Rico, Río Piedras Campus, PO Box 23346, San Juan, Puerto Rico, 00931, USA.

*Corresponding author. E-mail: jrivera{at}cnnet.upr.edu

Abstract

Guanine and G-rich oligonucleotides are known to self-assemble in the presence of a variety of cations to form higher ordered structures known as Gquadruplexes. We have synthesized a library of 8-aryl/heteroaryl-2'-deoxyguanosine derivatives (8ArGs) that are also able to self-assemble into quadruplex structures. We demonstrate that the properties of such quadruplexes can be modulated by the nature of the groups attached to the guanine base. These supramolecules are potentially useful in the development of self-assembled nanodevices.


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