Informace o publikaci

Polymorphism of human telomeric quadruplex structure controlled by DNA concentration: a Raman study

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PALACKÝ Jan VORLÍČKOVÁ Michaela KEJNOVSKÁ Iva MOJZEŠ Peter

Rok publikování 2013
Druh Článek v odborném periodiku
Časopis / Zdroj Nucleic Acids Research
Fakulta / Pracoviště MU

Středoevropský technologický institut

Citace
www http://nar.oxfordjournals.org/content/early/2012/11/26/nar.gks1135.full
Doi http://dx.doi.org/10.1093/nar/gks1135
Obor Biochemie
Klíčová slova NTRAMOLECULAR G-QUADRUPLEX; K+ SOLUTION; B-DNA; MELTING TRANSITIONS; POTASSIUM SOLUTION; POLARIZED RAMAN; NUCLEIC-ACIDS; SPECTROSCOPY; SEQUENCE; TETRAPLEX
Přiložené soubory
Popis DNA concentration has been recently suggested to be the reason why different arrangements are revealed for K+-stabilized human telomere quadruplexes by experimental methods requiring DNA concentrations differing by orders of magnitude. As Raman spectroscopy can be applied to DNA samples ranging from those accessible by absorption and CD spectroscopies up to extremely concentrated solutions, gels and even crystals; it has been used here to clarify polymorphism of a core human telomeric sequence G3(TTAG3)3 in the presence of K+and Na+ ions throughout wide range of DNA concentrations. We demonstrate that the K+-structure of G3(TTAG3)3 at low DNA concentration is close to the antiparallel fold of Na+-stabilized quadruplex. On the increase of G3(TTAG3)3 concentration, a gradual transition from antiparallel to intramolecular parallel arrangement was observed, but only for thermodynamically equilibrated K+-stabilized samples. The transition is synergically supported by increased K+ concentration. However, even for extremely high G3(TTAG3)3 and K+concentrations, an intramolecular antiparallel quadruplex is spontaneously formed from desalted non-quadruplex single-strand after addition of K+ ions. Thermal destabilization or long dwell time are necessary to induce interquadruplex transition. On the contrary, Na+-stabilized G3(TTAG3)3 retains its antiparallel folding regardless of the extremely high DNA and/or Na+concentrations, thermal destabilization or annealing.
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