Your browser doesn't support javascript.
loading
Crystallographic evidence of Watson-Crick connectivity in the base pair of anionic adenine with thymine.
Mishra, Manish Kumar; Kelley, Steven P; Smetana, Volodymyr; Dixon, David A; McNeill, Ashley S; Mudring, Anja-Verena; Rogers, Robin D.
Afiliación
  • Mishra MK; Department of Chemistry and Biochemistry, The University of Alabama, Tuscaloosa, AL 35487.
  • Kelley SP; Department of Chemistry and Biochemistry, The University of Alabama, Tuscaloosa, AL 35487.
  • Smetana V; Department of Materials and Environmental Chemistry, Stockholm University, Stockholm 106 91, Sweden.
  • Dixon DA; Department of Chemistry and Biochemistry, The University of Alabama, Tuscaloosa, AL 35487.
  • McNeill AS; Department of Chemistry and Biochemistry, The University of Alabama, Tuscaloosa, AL 35487.
  • Mudring AV; Department of Materials and Environmental Chemistry, Stockholm University, Stockholm 106 91, Sweden.
  • Rogers RD; Department of Chemistry and Biochemistry, The University of Alabama, Tuscaloosa, AL 35487; rdrogers@ua.edu.
Proc Natl Acad Sci U S A ; 117(31): 18224-18230, 2020 08 04.
Article en En | MEDLINE | ID: mdl-32680959
ABSTRACT
Utilizing an ionic liquid strategy, we report crystal structures of salts of free anionic nucleobases and base pairs previously studied only computationally and in the gas phase. Reaction of tetrabutylammonium ([N4444]+) or tetrabutylphosphonium ([P4444]+) hydroxide with adenine (HAd) and thymine (HThy) led to hydrated salts of deprotonated adenine, [N4444][Ad]·2H2O, and thymine, [P4444][Thy]·2H2O, as well as the double salt cocrystal, [P4444]2[Ad][Thy]·3H2O·2HThy. The cocrystal includes the anionic [Ad-(HThy)] base pair which is a stable formation in the solid state that has previously not even been suggested. It exhibits Watson-Crick connectivity as found in DNA but which is unusual for the free neutral base pairs. The stability of the observed anionic bases and their supramolecular formations and hydrates has also been examined by electronic structure calculations, contributing to more insight into how base pairs can bind when a proton is removed and highlighting mechanisms of stabilization or chemical transformation in the DNA chains.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Timina / Adenina / Emparejamiento Base Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Timina / Adenina / Emparejamiento Base Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2020 Tipo del documento: Article