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利用原子力显微镜在动态力谱中检测单键断裂。

On the detection of single bond ruptures in dynamic force spectroscopy by AFM.

机构信息

Department of Chemistry, Florida Institute of Technology, Melbourne, Florida 32901, USA.

出版信息

Langmuir. 2011 Sep 20;27(18):11287-91. doi: 10.1021/la202530j. Epub 2011 Aug 17.

Abstract

Force spectroscopy is a novel tool in physical chemistry and biophysics. This methodology is aimed at providing kinetic parameters of dissociation at a single-molecule level by rupturing molecular bonds subjected to different loading rates. One persistent problem in the implementation of this methodology is a question about the single-bond nature of the rupture events detected in experiments based on atomic force microscopy. Here we address this question by considering the probability that the nearly simultaneous rupture of two molecular bonds might appear as a single bond rupture in the experimental data, complicating the data analysis and contributing to systematic errors in the extracted kinetic parameters. An approximate analytical model predicts that such events might be common in experiments employing soft cantilever force sensors and short tethers to immobilize the interacting molecules. These findings are confirmed by a more elaborate numerical model providing valuable guidelines on performing single-molecule force spectroscopy experiments.

摘要

力谱学是物理化学和生物物理学中的一种新工具。该方法旨在通过在不同的加载速率下断裂分子键,提供单分子水平上的离解动力学参数。在实施这种方法时,一个持续存在的问题是关于基于原子力显微镜的实验中检测到的单键断裂事件的单一键性质的问题。在这里,我们通过考虑几乎同时断裂两个分子键的概率来解决这个问题,这可能会导致实验数据中的单键断裂,从而使数据分析复杂化,并导致提取的动力学参数出现系统误差。一个近似的分析模型预测,在使用软悬臂力传感器和短系链来固定相互作用的分子的实验中,这种事件可能很常见。这些发现得到了一个更精细的数值模型的证实,该模型提供了关于执行单分子力谱学实验的有价值的指导。

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