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嵌入分子诱导的DNA熵弹性转变。

Transition on the entropic elasticity of DNA induced by intercalating molecules.

作者信息

Rocha M S, Ferreira M C, Mesquita O N

机构信息

Departamento de Física, ICEx, Universidade Federal de Minas Gerais, Caixa Postal 702, Belo Horizonte, CEP 31270-901 Minas Gerais, Brazil.

出版信息

J Chem Phys. 2007 Sep 14;127(10):105108. doi: 10.1063/1.2768945.

Abstract

We use optical tweezers to perform stretching experiments on DNA molecules when interacting with the drugs daunomycin and ethidium bromide, which intercalate the DNA molecule. Our results show that the persistence length of the DNA-drug complexes increases strongly as the drug concentration increases up to some critical value. Above this critical value, the persistence length decreases abruptly and remains approximately constant for larger drug concentrations, at least in the concentration range used in our experiments. Measured intercalators critical concentrations for the persistence length transition coincide with the reported values for the helix-coil transition of DNA-drug complexes obtained from sedimentation experiments. The contour length of the molecules increases monotonically and saturates as the drug concentration increases. The neighbor exclusion model fits to our results for the total drug concentration as a function of the relative increase of the contour length.

摘要

我们使用光镊对与嵌入DNA分子的柔红霉素和溴化乙锭相互作用的DNA分子进行拉伸实验。我们的结果表明,随着药物浓度增加至某个临界值,DNA-药物复合物的持久长度会大幅增加。高于此临界值时,持久长度会突然减小,并且在更大的药物浓度下保持近似恒定,至少在我们实验所用的浓度范围内如此。测量得到的持久长度转变的嵌入剂临界浓度与通过沉降实验获得的DNA-药物复合物螺旋-卷曲转变的报道值相符。随着药物浓度增加,分子的轮廓长度单调增加并趋于饱和。邻域排斥模型符合我们关于总药物浓度作为轮廓长度相对增加量的函数的结果。

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