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热泳融解曲线定量描述 RNA 和 DNA 的构象和稳定性。

Thermophoretic melting curves quantify the conformation and stability of RNA and DNA.

机构信息

Physics Department and Center for NanoScience, Ludwig-Maximilians-Universität München, Amalienstrasse 54, 80799 München, Germany.

出版信息

Nucleic Acids Res. 2011 Apr;39(8):e52. doi: 10.1093/nar/gkr035. Epub 2011 Feb 4.

Abstract

Measuring parameters such as stability and conformation of biomolecules, especially of nucleic acids, is important in the field of biology, medical diagnostics and biotechnology. We present a thermophoretic method to analyse the conformation and thermal stability of nucleic acids. It relies on the directed movement of molecules in a temperature gradient that depends on surface characteristics of the molecule, such as size, charge and hydrophobicity. By measuring thermophoresis of nucleic acids over temperature, we find clear melting transitions and resolve intermediate conformational states. These intermediate states are indicated by an additional peak in the thermophoretic signal preceding most melting transitions. We analysed single nucleotide polymorphisms, DNA modifications, conformational states of DNA hairpins and microRNA duplexes. The method is validated successfully against calculated melting temperatures and UV absorbance measurements. Interestingly, the methylation of DNA is detected by the thermophoretic amplitude even if it does not affect the melting temperature. In the described setup, thermophoresis is measured all-optical in a simple setup using a reproducible capillary format with only 250 nl probe consumption. The thermophoretic analysis of nucleic acids shows the technique's versatility for the investigation of nucleic acids relevant in cellular processes like RNA interference or gene silencing.

摘要

测量生物分子,特别是核酸的稳定性和构象等参数,在生物学、医学诊断和生物技术领域非常重要。我们提出了一种热泳方法来分析核酸的构象和热稳定性。它依赖于分子在温度梯度中的定向运动,而温度梯度取决于分子的表面特性,如大小、电荷和疏水性。通过测量核酸在温度下的热泳,可以发现明显的熔解转变,并解析中间构象状态。在大多数熔解转变之前,热泳信号中出现的额外峰表明存在这些中间状态。我们分析了单核苷酸多态性、DNA 修饰、DNA 发夹和 microRNA 双链的构象状态。该方法成功地通过计算熔解温度和紫外吸收测量进行了验证。有趣的是,即使 DNA 的甲基化不影响熔解温度,也可以通过热泳幅度检测到。在所描述的设置中,热泳在一个简单的设置中全光学测量,使用可重复的毛细管格式,仅消耗 250nl 的探针。核酸的热泳分析表明,该技术在研究与细胞过程相关的核酸方面具有多功能性,如 RNA 干扰或基因沉默。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fc9/3082908/0e8b1f3774df/gkr035f2.jpg

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