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非平衡、近生理条件下氢键主客体体系的力学测量。

Mechanical measurement of hydrogen bonded host-guest systems under non-equilibrium, near-physiological conditions.

作者信息

Naranjo Teresa, Cerrón Fernando, Nieto-Ortega Belén, Latorre Alfonso, Somoza Álvaro, Ibarra Borja, Pérez Emilio M

机构信息

IMDEA Nanociencia , C/Faraday 9, Ciudad Universitaria de Cantoblanco , 28049 , Madrid , Spain . Email:

Nanobiotecnología (IMDEA-Nanociencia) , Unidad Asociada al Centro Nacional de Biotecnología (CSIC) , 28049 , Madrid , Spain.

出版信息

Chem Sci. 2017 Sep 1;8(9):6037-6041. doi: 10.1039/c7sc03044d. Epub 2017 Jul 31.

DOI:10.1039/c7sc03044d
PMID:28989633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5625567/
Abstract

Decades after the birth of supramolecular chemistry, there are many techniques to measure noncovalent interactions, such as hydrogen bonding, under equilibrium conditions. As ensembles of molecules rapidly lose coherence, we cannot extrapolate bulk data to single-molecule events under non-equilibrium conditions, more relevant to the dynamics of biological systems. We present a new method that exploits the high force resolution of optical tweezers to measure at the single molecule level the mechanical strength of a hydrogen bonded host-guest pair out of equilibrium and under near-physiological conditions. We utilize a DNA reporter to unambiguously isolate single binding events. The Hamilton receptor-cyanuric acid host-guest system is used as a test bed. The force required to dissociate the host-guest system is ∼17 pN and increases with the pulling rate as expected for a system under non-equilibrium conditions. Blocking one of the hydrogen bonding sites results in a significant decrease of the force-to-break by 1-2 pN, pointing out the ability of the method to resolve subtle changes in the mechanical strength of the binding due to the individual H-bonding components. We believe the method will prove to be a versatile tool to address important questions in supramolecular chemistry.

摘要

超分子化学诞生数十年后,已有许多技术可用于测量平衡条件下的非共价相互作用,比如氢键。由于分子集合体迅速失去相干性,我们无法将大量数据外推至非平衡条件下的单分子事件,而后者与生物系统的动力学更为相关。我们提出了一种新方法,该方法利用光镊的高力分辨率,在接近生理条件的非平衡状态下,于单分子水平测量氢键主客体对的机械强度。我们使用DNA报告分子来明确分离单个结合事件。以汉密尔顿受体-氰尿酸主客体系统作为测试平台。解离主客体系统所需的力约为17皮牛,并随着牵拉速率的增加而增大,这与非平衡条件下的系统预期相符。阻断其中一个氢键位点会导致断裂力显著降低1 - 2皮牛,这表明该方法能够分辨由于单个氢键组分导致的结合机械强度的细微变化。我们相信该方法将被证明是解决超分子化学重要问题的通用工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9a2/5625567/b6f4aef8f4fc/c7sc03044d-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9a2/5625567/7551299f51d1/c7sc03044d-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9a2/5625567/e5553c371a5d/c7sc03044d-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9a2/5625567/b6f4aef8f4fc/c7sc03044d-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9a2/5625567/7551299f51d1/c7sc03044d-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9a2/5625567/e5553c371a5d/c7sc03044d-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9a2/5625567/b6f4aef8f4fc/c7sc03044d-f3.jpg

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