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与柔性聚合物的耗尽相互作用导致巨型DNA的伸长/压缩。

Elongation/compaction of giant DNA caused by depletion interaction with a flexible polymer.

作者信息

Kojima M, Kubo K, Yoshikawa K

机构信息

Department of Physics, Graduate School of Science, Kyoto University, Kyoto, 606-8502, Japan.

出版信息

J Chem Phys. 2006 Jan 14;124(2):024902. doi: 10.1063/1.2145752.

Abstract

Structural changes in giant DNA induced by the addition of the flexible polymer Polyethylene Glycol (PEG) were examined by the method of single-DNA observation. In dilute DNA conditions, individual DNA assumes a compact state via a discrete coil-globule transition, whereas in concentrated solution, DNA molecules exhibit an extended conformation via macroscopic phase segregation. The long-axis length of the stretched state in DNA is about 10(3) times larger than that of the compact state. Phase segregation at high DNA concentrations occurs at lower PEG concentrations than the compaction at low DNA concentrations. These opposite changes in the conformation of DNA molecule are interpreted in terms of the free energy, including depletion interaction.

摘要

通过单DNA观察法研究了添加柔性聚合物聚乙二醇(PEG)引起的巨型DNA的结构变化。在稀DNA条件下,单个DNA通过离散的线圈-小球转变呈现紧凑状态,而在浓溶液中,DNA分子通过宏观相分离呈现伸展构象。DNA伸展状态下的长轴长度比紧凑状态下的长轴长度大约10³倍。高DNA浓度下的相分离在比低DNA浓度下的压缩更低的PEG浓度时发生。DNA分子构象的这些相反变化根据包括排空相互作用在内的自由能来解释。

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