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以纳米级精度直接观察不匹配诱导 DNA 泡的呼吸动力学:smFRET 研究。

Direct observation of breathing dynamics at the mismatch induced DNA bubble with nanometre accuracy: a smFRET study.

机构信息

Chemical Sciences Division, Saha Institute of Nuclear Physics, 1/AF Bidhannagar, Kolkata 700064, India.

出版信息

Nanoscale. 2017 May 11;9(18):5835-5842. doi: 10.1039/c6nr09348e.

Abstract

The detailed conformational dynamics of the melted region in double-stranded DNA has been studied using a combination of ensemble and single-molecule FRET techniques. We monitored the millisecond time scale fluctuation kinetics of the two strands at the bubble region that varies with the size of the bubble. As the individual strands at the melting bubble behave as single-stranded DNA, and hence fluctuate dynamically to attain energetically favored configurations, the rates of these fluctuations increase with increase in the bubble size. In different short DNAs under investigation, the two strands never cross each other to form a knot, irrespective of the number of base pair mismatches present. Rather, they prefer to stay apart from each other, as the size of the bubble increases and follow exactly an opposite trend for bubbles of smaller size. The range within which the bubble strands fluctuate are monitored with great accuracy in the nanometre resolution from the single-molecule FRET measurements. The shape of the bubble that plays a crucial role in determining the activity of the DNA was speculated. These results shall be useful in quantifying the chemical processes within DNA as well as to develop a deeper understanding of the activity of the DNA due to induced mismatches.

摘要

使用组合的集合和单分子 FRET 技术研究了双链 DNA 中融化区域的详细构象动力学。我们监测了随泡大小变化的泡区中两条链的毫秒时间尺度波动动力学。由于熔融泡处的各个链表现为单链 DNA,因此会动态波动以达到能量有利的构象,这些波动的速率随泡大小的增加而增加。在所研究的不同短 DNA 中,两条链从不相互交叉形成结,无论存在多少碱基对错配。相反,随着泡的增大,它们更喜欢彼此分开,并遵循与较小泡相反的趋势。通过单分子 FRET 测量以纳米分辨率非常精确地监测泡链波动的范围。推测了在确定 DNA 活性中起关键作用的泡的形状。这些结果将有助于量化 DNA 内的化学过程,并深入了解由于诱导错配而导致的 DNA 活性。

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