The full text of this article hosted at iucr.org is unavailable due to technical difficulties.

Angewandte Chemie
Zuschrift

yDNA: A New Geometry for Size‐Expanded Base Pairs*

Haige Lu

Department of Chemistry, Stanford University, Stanford, CA 94305‐5080, USA, Fax: (+1) 650‐725‐0259

Search for more papers by this author
Kaizhang He Dr.

Department of Chemistry, Stanford University, Stanford, CA 94305‐5080, USA, Fax: (+1) 650‐725‐0259

Search for more papers by this author
Eric T. Kool Prof. Dr.

E-mail address:kool@leland.stanford.edu

Department of Chemistry, Stanford University, Stanford, CA 94305‐5080, USA, Fax: (+1) 650‐725‐0259

Search for more papers by this author
First published: 02 November 2004
Cited by: 11
*

This work was supported by the U.S. National Institutes of Health (GM63587) and by an Abbott Laboratories Graduate Research Fellowship to H.L.

Abstract

Neue Paarung: Die Insertion eines Benzolrings in den natürlichen Adeninheterocyclus führt zum Analogon yA und zur Bildung von Basenpaaren, die 2.4 Å breiter sind als die natürlichen Basenpaare (siehe Struktur). Die Paare yA⋅T und T⋅yA können sich zu kooperativen Helices zusammenlagern, die deutlich stabiler als natürliche DNA sind. Demzufolge könnte yDNA ein Kandidat für ein neues genetisches System sein.

Number of times cited: 11

  • , Theoretical study on absorption and emission spectra of pyrrolo-C analogues, Journal of Molecular Structure, 10.1016/j.molstruc.2014.06.041, 1079, (321-326), (2015).
  • , Theoretical study on absorption and emission spectra of adenine analogues, Journal of Molecular Modeling, 10.1007/s00894-014-2100-4, 20, 4, (2014).
  • , Theoretical study of the structural and optical properties of cytosine analogues, Computational and Theoretical Chemistry, 10.1016/j.comptc.2014.09.026, 1049, (75-81), (2014).
  • , Künstliche genetische Systeme bestehend aus vergrößerten Basenpaaren, Angewandte Chemie, 125, 48, (12728-12739), (2013).
  • , Artificial Genetic Sets Composed of Size‐Expanded Base Pairs, Angewandte Chemie International Edition, 52, 48, (12498-12508), (2013).
  • , Computational investigation of thermochemical properties of non-natural C-nucloebases: different hydrogen-bonding preferences for non-natural Watson–Crick base pairs, Structural Chemistry, 10.1007/s11224-012-0115-y, 24, 4, (1015-1025), (2012).
  • , A Nucleobase‐Discriminating Pyrrolo‐dC Click Adduct Designed for DNA Fluorescence Mismatch Sensing, Chemistry – A European Journal, 18, 31, (9590-9600), (2012).
  • , Polymerase Amplification, Cloning, and Gene Expression of Benzo‐Homologous “yDNA” Base Pairs, ChemBioChem, 9, 18, (2976-2980), (2008).
  • , Assembly of the Complete Eight‐Base Artificial Genetic Helix, xDNA, and Its Interaction with the Natural Genetic System, Angewandte Chemie, 117, 20, (3178-3182), (2005).
  • , Organische Chemie 2004, Nachrichten aus der Chemie, 53, 3, (251-272), (2010).
  • , Assembly of the Complete Eight‐Base Artificial Genetic Helix, xDNA, and Its Interaction with the Natural Genetic System, Angewandte Chemie International Edition, 44, 20, (3118-3122), (2005).