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Molecules ; 18(10): 12751-67, 2013 Oct 15.
Artigo em Inglês | MEDLINE | ID: mdl-24132198

RESUMO

We have previously shown that c-MYC promoter sequences can form stable i-motifs in acidic solution (pH 4.5-5.5). In terms of drug targeting, the question is whether c-MYC promoter sequence i-motifs will exist in the nucleus at neutral pH. In this work, we have investigated the stability of a mutant c-MYC i-motif in solutions containing a molecular crowding agent. The crowded nuclear environment was modeled by the addition of up to 40% w/w polyethylene glycols having molecular weights up to 12,000 g/mol. CD and DSC were used to establish the presence and stability of c-MYC i-motifs in buffer solutions over the pH range 4 to 7. We have shown that the c-MYC i-motif can exist as a stable structure at pH values as high as 6.7 in crowded solutions. Generic dielectric constant effects, e.g., a shift in the pKa of cytosine by more than 2 units (e.g., 4.8 to 7.0), or the formation of non-specific PEG/DNA complexes appear to contribute insignificantly to i-motif stabilization. Molecular crowding, largely an excluded volume effect of added PEG, having a molecular weight in excess of 1,000 g/mol, appears to be responsible for stabilizing the more compact i-motif over the random coil at higher pH values.


Assuntos
Regiões Promotoras Genéticas , Proteínas Proto-Oncogênicas c-myc/genética , Sequência de Bases , Varredura Diferencial de Calorimetria , Dicroísmo Circular , DNA/química , DNA/genética , Humanos , Concentração de Íons de Hidrogênio , Conformação de Ácido Nucleico , Polietilenoglicóis/química , Soluções , Temperatura de Transição
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