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The Effect of Molecular Crowding on the Stability of Human c-MYC Promoter Sequence I-Motif at Neutral pH

机译:分子拥挤对中性pH下人c-MYC启动子序列I-Motif稳定性的影响

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摘要

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.
机译:我们以前已经证明c-MYC启动子序列可以在酸性溶液(pH 4.5-5.5)中形成稳定的i-基序。在药物靶向方面,问题是在中性pH下c-MYC启动子序列的i-基序是否会存在于细胞核中。在这项工作中,我们研究了突变的c-MYC i-基序在含有分子拥挤剂的溶液中的稳定性。通过添加分子量高达12,000 g / mol的高达40%w / w聚乙二醇来模拟拥挤的核环境。 CD和DSC用于建立pH范围为4到7的缓冲溶液中c-MYC i-基序的存在和稳定性。我们已经证明,c-MYC i-基序可以在pH值如下的情况下以稳定结构存在。在拥挤的解决方案中最高为6.7。通用介电常数效应,例如胞嘧啶的pKa位移超过2个单位(例如4.8至7.0),或者非特异性PEG / DNA复合物的形成似乎对i-基序稳定的作用微不足道。分子拥挤在很大程度上排除了添加的PEG的体积效应,分子量超过1,000 g / mol,这似乎是在较高pH值下稳定了随机线圈上更紧密的i-基序的原因。

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