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测量受谐和约束的生物聚合物的折叠景观。

Measuring the folding landscape of a harmonically constrained biopolymer.

机构信息

Department of Physics, Institute for Physical Science and Technology Biophysics Program, University of Maryland, College Park, Maryland, USA.

出版信息

Biophys J. 2011 Jun 8;100(11):2736-44. doi: 10.1016/j.bpj.2011.03.067.

Abstract

Pioneering studies have shown that the probability distribution of opening length for a DNA hairpin, recorded under constant force using an optical trap, can be used to reconstruct the energy landscape of the transition. However, measurements made under constant force are subject to some limitations. Under constant force a system with a sufficiently high energy barrier spends most of its time in the closed or open conformation, with relatively few statistics collected in the transition state region. We describe a measurement scheme in which the system is driven progressively through the transition by an optical trap and an algorithm is used to extract the energy landscape of the transition from the fluctuations recorded during this process. We illustrate this technique in simulations and demonstrate its effectiveness in experiments on a DNA hairpin. We find that the combination of this technique with the use of short DNA handles facilitates a high-resolution measurement of the hairpin's folding landscape with a very short measurement time.

摘要

开创性的研究表明,使用光阱在恒力下记录的 DNA 发夹的开口长度概率分布可用于重构跃迁的能量景观。然而,在恒力下进行的测量受到一些限制。在恒力下,能量势垒足够高的系统大部分时间处于闭合或开放构象,在过渡状态区域中收集的统计数据相对较少。我们描述了一种测量方案,其中系统通过光阱逐渐驱动过渡,并且使用算法从该过程中记录的波动中提取过渡的能量景观。我们在模拟中说明了该技术,并在 DNA 发夹的实验中证明了其有效性。我们发现,将该技术与短 DNA 手柄的使用相结合,可在非常短的测量时间内实现发夹折叠景观的高分辨率测量。

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Single-molecule derivation of salt dependent base-pair free energies in DNA.单分子方法测定 DNA 中盐依赖的碱基对自由能。
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Theory, analysis, and interpretation of single-molecule force spectroscopy experiments.单分子力谱实验的理论、分析与解释
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The protein folding problem.蛋白质折叠问题。
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Single-molecule studies of protein folding.蛋白质折叠的单分子研究。
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