Literature DB >> 12670232

Formation of a PNA2-DNA2 hybrid quadruplex.

Bhaskar Datta1, Christoph Schmitt, Bruce A Armitage.   

Abstract

DNA guanine (G) quadruplexes are stabilized by an interesting variation of the hydrogen-bonding schemes encountered in nucleic acid duplexes and triplexes. In an attempt to use this mode of molecular recognition, we target a dimeric G-quadruplex formed by the Oxytricha nova telomeric sequence d(G(4)T(4)G(4)) with a peptide nucleic acid (PNA) probe having a homologous rather than complementary sequence. UV-vis and CD spectroscopy reveal that a stable hybrid possessing G-quartets is formed between the PNA and DNA. The four-stranded character of the hybrid and the relative orientation of the strands is determined by fluorescence resonance energy transfer (FRET) experiments. FRET results indicate that (i) the two PNA strands are parallel to each other, (ii) the two DNA strands are parallel to each other, and (iii) the 5'-termini of the DNA strands align with the N-termini of the PNA strands. The resulting PNA(2)-DNA(2) quadruplex shows a preference of Na(+) over Li(+) and displays thermodynamic behavior consistent with alternating PNA and DNA strands in the hybrid. The formation of this novel supramolecular structure demonstrates a new high-affinity DNA recognition mechanism and expands the scope of molecular recognition by PNA.

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Year:  2003        PMID: 12670232     DOI: 10.1021/ja028323d

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  24 in total

1.  NMR solution structure of a parallel LNA quadruplex.

Authors:  Antonio Randazzo; Veronica Esposito; Oliver Ohlenschläger; Ramadurai Ramachandran; Luciano Mayola
Journal:  Nucleic Acids Res       Date:  2004-06-04       Impact factor: 16.971

Review 2.  Targeting DNA G-quadruplex structures with peptide nucleic acids.

Authors:  Igor G Panyutin; Mykola I Onyshchenko; Ethan A Englund; Daniel H Appella; Ronald D Neumann
Journal:  Curr Pharm Des       Date:  2012       Impact factor: 3.116

3.  (3 + 1) Assembly of three human telomeric repeats into an asymmetric dimeric G-quadruplex.

Authors:  Na Zhang; Anh Tuân Phan; Dinshaw J Patel
Journal:  J Am Chem Soc       Date:  2005-12-14       Impact factor: 15.419

4.  Hybridization of complementary and homologous peptide nucleic acid oligomers to a guanine quadruplex-forming RNA.

Authors:  Violeta L Marin; Bruce A Armitage
Journal:  Biochemistry       Date:  2006-02-14       Impact factor: 3.162

5.  Noncovalent binding and fluorogenic response of cyanine dyes to DNA homoquadruplex and PNA-DNA heteroquadruplex structures.

Authors:  Halimatu S Mohammed; Junriz O Delos Santos; Bruce A Armitage
Journal:  Artif DNA PNA XNA       Date:  2011-04

6.  G-quadruplex formation between G-rich PNA and homologous sequences in oligonucleotides and supercoiled plasmid DNA.

Authors:  Timur I Gaynutdinov; Ethan A Englund; Daniel H Appella; Mykola I Onyshchenko; Ronald D Neumann; Igor G Panyutin
Journal:  Nucleic Acid Ther       Date:  2015-02-04       Impact factor: 5.486

7.  Homologous PNA Hybridization to Noncanonical DNA G-Quadruplexes.

Authors:  Karen A Kormuth; John L Woolford; Bruce A Armitage
Journal:  Biochemistry       Date:  2016-03-16       Impact factor: 3.162

8.  Multivalent LKγ-PNA oligomers bind to a human telomere DNA G-rich sequence to form quadruplexes.

Authors:  Pankaj Gupta; Elizabeth E Rastede; Daniel H Appella
Journal:  Bioorg Med Chem Lett       Date:  2015-07-29       Impact factor: 2.823

9.  Loop and backbone modifications of peptide nucleic acid improve g-quadruplex binding selectivity.

Authors:  Sabrina Lusvarghi; Connor T Murphy; Subhadeep Roy; Farial A Tanious; Iulia Sacui; W David Wilson; Danith H Ly; Bruce A Armitage
Journal:  J Am Chem Soc       Date:  2009-12-30       Impact factor: 15.419

10.  Strand invasion of DNA quadruplexes by PNA: comparison of homologous and complementary hybridization.

Authors:  Anisha Gupta; Ling-Ling Lee; Subhadeep Roy; Farial A Tanious; W David Wilson; Danith H Ly; Bruce A Armitage
Journal:  Chembiochem       Date:  2013-07-19       Impact factor: 3.164

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