4.6 Article

Examination of the Effect of the Annealing Cation on Higher Order Structures Containing Guanine or Isoguanine Repeats

期刊

CHEMISTRY-A EUROPEAN JOURNAL
卷 15, 期 42, 页码 11244-11255

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.200901047

关键词

DNA structures; isoguanine; mass spectrometry; supramolecular chemistry

资金

  1. Robert A. Welch Foundation [F-1155]
  2. National Institutes of Health [RO1 GM65956]
  3. National Science Foundation [CHE750357]
  4. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM065956] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Isoguanine (2-oxo-6-aminoguanine), a natural but non-standard base, exhibits unique self-association properties compared to its isomer, guanine, and results in formation of different higher order DNA structures. In this work, the higher order structures formed by oligonucleotides containing guanine repeats or isoguanine repeats after annealing in solutions containing various cations are evaluated by electrospray ionization mass spectrometry (ESI-MS) and Circular dichroism (CD) spectroscopy. The guanine-containing strand (G9) consistently formed quadruplexes upon annealing, whereas the isoguanine strand (Ig9) formed both pentaplexes and quadruplexes depending on the annealing cation. Quadruplex formation with G9 showed some dependence on the identity of the cation present during annealing with high relative quadruplex formation detected with six of ten cations. Analogous annealing experiments with Ig9 resulted in complex formation with all ten cations, and the majority of the resulting complexes were pentaplexes. CD results indicated most of the original complexes survived the desalting process necessary for ESI-MS analysis. In addition, several complexes, especially the pentaplexes, were found to be capable of cation exchange with ammonium ions. Ab initio calculations were conducted for isoguanine tetrads and pentads coordinated with all ten cations to predict the most energetically stable structures of the complexes in the gas phase. The observed preference of forming quadruplexes versus pentaplexes as a function of the coordinated cation can be interpreted by the calculated reaction energies of both the tetrads and pentads in combination with the distortion energies of tetrads.

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