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Synthesis of quadruplex-forming tetra-end-linked oligonucleotides: Effects of the linker size on quadruplex topology and stability

Authors

  • Giorgia Oliviero,

    1. Dipartimento di Chimica delle Sostanze Naturali, Università degli Studi di Napoli “Federico II,” Via D. Montesano 49, I-80131 Napoli, Italy
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  • Nicola Borbone,

    1. Dipartimento di Chimica delle Sostanze Naturali, Università degli Studi di Napoli “Federico II,” Via D. Montesano 49, I-80131 Napoli, Italy
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  • Jussara Amato,

    1. Dipartimento di Chimica delle Sostanze Naturali, Università degli Studi di Napoli “Federico II,” Via D. Montesano 49, I-80131 Napoli, Italy
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  • Stefano D'Errico,

    1. Dipartimento di Chimica delle Sostanze Naturali, Università degli Studi di Napoli “Federico II,” Via D. Montesano 49, I-80131 Napoli, Italy
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  • Aldo Galeone,

    1. Dipartimento di Chimica delle Sostanze Naturali, Università degli Studi di Napoli “Federico II,” Via D. Montesano 49, I-80131 Napoli, Italy
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  • Gennaro Piccialli,

    Corresponding author
    1. Dipartimento di Chimica delle Sostanze Naturali, Università degli Studi di Napoli “Federico II,” Via D. Montesano 49, I-80131 Napoli, Italy
    • Dipartimento di Chimica delle Sostanze Naturali, Università degli Studi di Napoli “Federico II,” Via D. Montesano 49, I-80131 Napoli, Italy
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  • Michela Varra,

    1. Dipartimento di Chimica delle Sostanze Naturali, Università degli Studi di Napoli “Federico II,” Via D. Montesano 49, I-80131 Napoli, Italy
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  • Luciano Mayol

    1. Dipartimento di Chimica delle Sostanze Naturali, Università degli Studi di Napoli “Federico II,” Via D. Montesano 49, I-80131 Napoli, Italy
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Abstract

G-quadruplexes are characteristic structural arrangements of guanine-rich DNA sequences that abound in regions with relevant biological significance. These structures are highly polymorphic differing in the number and polarity of the strands, loop composition, and conformation. Furthermore, the cation species present in solution strongly influence the topology of the G-quadruplexes. Recently, we reported the synthesis and structural studies of new G-quadruplex forming oligodeoxynucleotides (ODNs) in which the 3′- and/or the 5′-ends of four ODN strands are linked together by a non-nucleotidic tetra-end-linker (TEL). These TEL-ODN analogs having the sequence TGGGGT are able to form parallel G-quadruplexes characterized by a remarkable high thermal stability. We report here an investigation about the influence of the reduction of the TEL size on the molecularity, topology, and stability of the resulting TEL-G-quadruplexes using a combination of circular dichroism (CD), CD melting, 1H NMR spectroscopy, gel electrophoresis, and molecular modeling data. We found that all TEL-(TGGGGT)4 analogs, regardless the TEL size and the structural orientation of the ODN branches, formed parallel TEL-G-quadruplexes. The molecular modeling studies appear to be consistent with the experimental CD and NMR data revealing that the G-quadruplexes formed by TEL-ODNs having the longer TEL (L1-4) are more stable than the corresponding G-quadruplexes having the shorter TEL (S1-4). The relative stability of S1-4 was also reported. © 2009 Wiley Periodicals, Inc. Biopolymers 91: 466–477, 2009.

This article was originally published online as an accepted preprint. The “Published Online” date corresponds to the preprint version. You can request a copy of the preprint by emailing the Biopolymers editorial office at biopolymers@wiley.com

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