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表面固定双链 DNA 和配体-载脂蛋白复合物的结合亲和力和动力学的朗缪尔分析。

Langmuir Analysis of the Binding Affinity and Kinetics for Surface Tethered Duplex DNA and a Ligand-Apoprotein Complex.

机构信息

Organic Chemistry, Chem. Biol. Dept., Faculty IV , Siegen University , Adolf-Reichwein-Str. 2 , 57068 Siegen , Germany.

出版信息

Langmuir. 2018 Dec 11;34(49):14738-14748. doi: 10.1021/acs.langmuir.7b04347. Epub 2018 Jul 30.

Abstract

In this work, the hybridization and dehybridization of ssDNA with 20 bases at gold coated sensor surfaces modified with complementary 20 bases capture probe ssDNA was investigated at 18 °C by quartz crystal microbalance measurements with dissipation monitoring (QCM-D). A sequence of 20 base pairs with a melting temperature of about 64 °C was chosen, since in many biosensor studies the target molecules are DNA or RNA oligomers of similar length. It turned out that at the applied experimental conditions the DNA hybridization was irreversible, and therefore the hybridization and dehybridization process could not be described by the Langmuir model of adsorption. Nevertheless, quantitative dehybridization could be achieved by rinsing the sensor surface thoroughly with pure water. When in contrast the hybridization of a target with only 10 bases complementary to the outermost 10 bases of the 20 bases capture probe was studied, binding and unbinding were reversible, and the hybridization/dehybridization process could be satisfactorily described by the Langmuir model. For the 10 base pair sequence, the melting temperature was about 36 °C. Apparently, for Langmuir behavior, it is important that the experiments are applied at a temperature sufficiently close to the melting temperature of the sequence under investigation to ensure that at least traces of the target molecules are unhybridized (i.e., there needs to be an equilibrium between hybridized and dehybridized target molecules). To validate the reliability of our experimental approach we also studied the reconstitution and disassembly of the flavoprotein dodecin at flavin-terminated DNA monolayers, as according to previous studies it is assumed that the apododecin-flavin system can be well described by the Langmuir model. As a result, this assumption could be verified. Using three different approaches, K values were obtained that differ not more than by a factor of 4.

摘要

在这项工作中,通过石英晶体微天平测量结合耗散监测(QCM-D)研究了在 18°C 下金涂覆传感器表面的 ssDNA 与互补 20 个碱基的捕获探针 ssDNA 的杂交和去杂交。选择了具有约 64°C 熔点的 20 个碱基对序列,因为在许多生物传感器研究中,靶分子是类似长度的 DNA 或 RNA 寡聚物。结果表明,在所应用的实验条件下,DNA 杂交是不可逆的,因此杂交和解杂交过程不能用 Langmuir 吸附模型来描述。尽管如此,通过用纯水彻底冲洗传感器表面仍然可以实现定量去杂交。相比之下,当研究仅与 20 个碱基捕获探针的最外 10 个碱基互补的靶标分子的杂交时,结合和解离是可逆的,并且可以用 Langmuir 模型令人满意地描述杂交/去杂交过程。对于 10 个碱基对序列,熔点约为 36°C。显然,对于 Langmuir 行为,重要的是在足够接近研究序列的熔点的温度下进行实验,以确保至少有痕量的靶分子未杂交(即,需要在杂交和去杂交的靶分子之间存在平衡)。为了验证我们实验方法的可靠性,我们还研究了黄素末端 DNA 单层上十二肽黄素蛋白的重组和解体,因为根据先前的研究,假定无侧链的十二肽-黄素系统可以很好地用 Langmuir 模型来描述。结果,验证了这一假设。使用三种不同的方法,获得了差异不超过 4 倍的 K 值。

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