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Kinetics of transient end-to-end contact of single-stranded DNAs

机译:单链DNA端到端瞬时接触的动力学

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The formation of the pyrene (Py) dimer radical cation (PY2center dot+) was used to measure the kinetics of the intrastrand end-to-end contact rates of single-stranded DNAs (ssDNAs) in the 10 nanoseconds to the tens of microseconds time range. ssDNAs labeled with Py at both ends with the lengths of 3, 6, and 9 mer were synthesized, and the two-photon ionization method was employed to generate a Pycenter dot+, which enables the measurements of the end-to-end contact rates from 10 ns. The formation rate of PY2center dot+ depended on the length and the sequence of the ssDNAs, and about 1 order of magnitude faster rates were observed for the T-rich ssDNAs compared to those for the corresponding length of A-rich ssDNAs, showing that ssDNA made from adenines is much more rigid than thatcomposed of thymidines. As forthe T-rich ssDNAs, the formation Of PY2center dot+ attributed to the misfolded structures was also observed, which is consistent with the configurational diffusion model suggested by Ansari and co-workers.
机译:((Py)二聚体自由基阳离子(PY2center dot +)的形成用于测量10纳秒至数十微秒时间范围内的单链DNA(ssDNA)的链内端对端接触速率的动力学。合成了分别用3,6和9 mer长度标记为Py的ssDNA,并采用双光子电离方法生成Pycenter dot +,从而可以测量从10 ns。 PY2center dot +的形成速率取决于ssDNA的长度和序列,与相应长度的A富集ssDNA相比,富T的ssDNA的观察到的速率快约1个数量级,表明ssDNA可以腺嘌呤的胸腺嘧啶比胸腺嘧啶核苷的硬得多。至于富含T的ssDNA,也观察到归因于错误折叠结构的PY2center dot +的形成,这与Ansari及其同事提出的构型扩散模型是一致的。

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