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Label-free and Non-destruction Determination of Single- and Double-Strand DNA based on Quantum Weak Measurement

机译:基于量子弱测量的单链和双链DNA的无标记无损测定

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摘要

The process of unwinding and renaturation of DNA has been widely used in studies of nucleotide sequence organization. Compared with traditional methods for DNA unwinding and renaturation, the label-free and non-destruction detection technology is significant and desiderated. We realized an optical system based on optical rotation via weak measurement for detection of single- and double-strand state of DNA. The optical rotation, which was induced by the status change of single and double DNA strands, was exploited to modulate the preselected polarization of a weak measurement system. With this modulation, the optical rotation caused by the separation of DNA strands can be determined through the center wavelength shift of the output spectrum. By monitoring the wavelength shift in real time, the separation processes of the DNAs with different base ratio (25% and 70%) and length (4nt and 40nt), and DNAs with three terminally modified cholesterol molecules were experimentally explored in varied pH and temperature conditions. In addition, the detection limit of the DNA concentration was obtained to be 5 × 10−6 mol/L. Our work based on optical rotation detection of single- and double-strand DNA exhibits the unique advantages of real-time monitoring, label-free, non-destruction and simplicity.
机译:DNA的展开和复性过程已广泛用于核苷酸序列组织的研究。与传统的DNA解链和复性方法相比,无标记和无破坏的检测技术意义重大且值得商side。我们通过弱测量实现了基于旋光的光学系统,用于检测DNA的单链和双链状态。由单链和双链DNA的状态变化引起的旋光被用于调制弱测量系统的预选极化。通过这种调制,可以通过输出光谱的中心波长偏移来确定由DNA链分离引起的旋光。通过实时监测波长变化,在不同的pH和温度下,实验探索了具有不同碱基比率(25%和70%)和长度(4nt和40nt)的DNA以及具有三个末端修饰的胆固醇分子的DNA的分离过程。条件。另外,DNA浓度的检出限为5××10 10 sup-6 smol / L。我们基于单链和双链DNA旋光检测的工作展现了实时监控,无标记,无破坏和简单的独特优势。

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