Medical Journals

Metal Binding to Bipyridine-modified Pna.

Authors:
  • Franzini Raphael M
  • Watson Richard M
  • Patra Goutam K
  • Breece Robert M
  • Tierney David L
  • Hendrich Michael P
  • Achim Catalina

From: Department of Chemistry, Carnegie Mellon University, 4400 5th Avenue, Pittsburgh, Pennsylvania 15213, USA.

Inorganic chemistry

  • Publish Date: Nov 2006
  • ISSN: 0020-1669
  • Volume: 45
  • Issue: 24
  • Pages: 9798-811
  • Medium: Print
  • Language: English
  • Citation (JAMA): Franzini Raphael M, Watson Richard M, Patra Goutam K, et al. Metal Binding to Bipyridine-modified Pna.. Nov 2006;45:9798-811

Abstract

Substitution of natural nucleobases in PNA oligomers with ligands is a strategy for directing metal ion incorporation to specific locations within a PNA duplex. In this study, we have synthesized PNA oligomers that contain up to three adjacent bipyridine ligands and examined the interaction with Ni2+ and Cu2+ of these oligomers and of duplexes formed from them. Variable-temperature UV spectroscopy showed that duplexes containing one terminal pair of bipyridine ligands are more stable upon metal binding than their nonmodified counterparts. While binding of one metal ion to duplexes that contain two adjacent bipyridine pairs makes the duplexes more stable, additional metal ions lower the duplex stability, with electrostatic repulsions being, most likely, an important contributor to the destabilization. UV titrations showed that the presence of several bipyridine ligands in close proximity of each other in PNA oligomers exerts a chelate effect. A supramolecular chelate effect occurs when several bipyridines are brought next to each other by hybridization of PNA duplexes. EPR spectroscopy studies indicate that even when two Cu2+ ions coordinate to a PNA duplex in which two bipyridine pairs are next to each other, the two metal-ligand complexes that form in the duplex are far enough from each other that the dipolar coupling is very weak. EXAFS and XANES show that the Ni2+-bipyridine bond lengths are typical for [Ni(bipy)2]2+ and [Ni(bipy)3]2+ complexes.

Mesh Headings (Keywords): 2,2’-Dipyridyl, Base Pairing, Binding Sites, Cobalt, Copper, Electron Spin Resonance Spectroscopy, Ligands, Metals, Nickel, Peptide Nucleic Acids, Titrimetry, Ultraviolet Rays


Check for Full Text / PubMed Unique Identifier (PMID): 17112277


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The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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