Literature DB >> 14750800

Synthesis of DNA with phenanthridinium as an artificial DNA base.

Robert Huber1, Nicole Amann, Hans-Achim Wagenknecht.   

Abstract

A phenanthridinium-containing DNA building block was synthesized as an ethidium nucleoside analogue starting from 3,8-diamino-6-phenyl-phenanthridine. Using this building block, oligonucleotides bearing the phenanthridinium moiety as an artificial DNA base were prepared via automated solid-phase phosphoramidite chemistry. The modified phenanthridinium-containing DNA duplexes were characterized by UV/vis absorption spectroscopy (including the melting behavior), CD spectroscopy, and steady-state fluorescence spectroscopy. These experiments reveal the expected similarity of the synthetic phenanthridinium moiety with noncovalently bound ethidium. More importantly, the results show clearly that the artificial phenanthridinium base is intercalated within the DNA base stack. The counterbase as part of the complementary strand seems to have only a minor influence on the intercalation properties of the phenanthridinium moiety.

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Year:  2004        PMID: 14750800     DOI: 10.1021/jo0355404

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  7 in total

1.  Base pair motions control the rates and distance dependencies of reductive and oxidative DNA charge transfer.

Authors:  Linda Valis; Qiang Wang; Milen Raytchev; Ivan Buchvarov; Hans-Achim Wagenknecht; Torsten Fiebig
Journal:  Proc Natl Acad Sci U S A       Date:  2006-06-26       Impact factor: 11.205

Review 2.  DNA-multichromophore systems.

Authors:  Yin Nah Teo; Eric T Kool
Journal:  Chem Rev       Date:  2012-03-16       Impact factor: 60.622

3.  Synthetic incorporation of Nile Blue into DNA using 2'-deoxyriboside substitutes: Representative comparison of (R)- and (S)-aminopropanediol as an acyclic linker.

Authors:  Daniel Lachmann; Sina Berndl; Otto S Wolfbeis; Hans-Achim Wagenknecht
Journal:  Beilstein J Org Chem       Date:  2010-02-09       Impact factor: 2.883

4.  Electrophilic chemistry of thia-PAHs: stable carbocations (NMR and DFT), S-alkylated onium salts, model electrophilic substitutions (nitration and bromination), and mutagenicity assay.

Authors:  Kenneth K Laali; Joong-Hyun Chun; Takao Okazaki; Subodh Kumar; Gabriela L Borosky; Carol Swartz
Journal:  J Org Chem       Date:  2007-10-02       Impact factor: 4.354

5.  Expanding the palette of phenanthridinium cations.

Authors:  Andrew G Cairns; Hans Martin Senn; Michael P Murphy; Richard C Hartley
Journal:  Chemistry       Date:  2014-03-24       Impact factor: 5.236

Review 6.  Come-back of phenanthridine and phenanthridinium derivatives in the 21st century.

Authors:  Lidija-Marija Tumir; Marijana Radić Stojković; Ivo Piantanida
Journal:  Beilstein J Org Chem       Date:  2014-12-10       Impact factor: 2.883

7.  Synthesis of Wavelength-Shifting Fluorescent DNA and RNA with Two Photostable Cyanine-Styryl Dyes as the Base Surrogate Pair.

Authors:  Jeannine Steinmeyer; Franziska Rönicke; Ute Schepers; Hans-Achim Wagenknecht
Journal:  ChemistryOpen       Date:  2017-06-07       Impact factor: 2.911

  7 in total

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