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由受限聚合物排斥剂和配体-受体键介导的分子粘附稳定性。

Stability of molecular adhesion mediated by confined polymer repellers and ligand-receptor bonds.

作者信息

Wang Jizeng, Qian Jin, Gao Huajian

机构信息

Division of Engineering, Box D, Brown University, 182 Hope Street, Providence, RI 02912, USA.

出版信息

Mol Cell Biomech. 2008 Mar;5(1):19-25.

Abstract

Experiments have shown that stable adhesion of a variety of animal cells on substrates prepared with precisely controlled ligand distribution can be formed only if the ligand spacing is below 58 nm. To explain this phenomenon, here we propose a confined polymer model to study the stability of molecular adhesion mediated by polymer repellers and ligand-receptor bonds. In this model, both repellers and binders are treated as wormlike chains confined in a nanoslit, and the stability of adhesion is considered as a competition between attractive interactions of ligand-receptor binding and repulsive forces due to the size mismatch between repellers and binders. The force on each ligand-receptor bond is calculated from the confined polymer model, and the classic model of Bell is used to describe the association/dissociation reactions of ligand-receptor bonds. The calculated equilibrium bond distribution shows that there exists a critical ligand density for stable adhesion, corresponding to a critical ligand spacing which agrees not only qualitatively but also quantitatively with the experimental observation. In the case of stable adhesion, the model predicts an equilibrium separation between adhesion surfaces below 60% of the contour length of the ligand-receptor bonds.

摘要

实验表明,只有当配体间距低于58纳米时,多种动物细胞才能在配体分布精确控制的基质上形成稳定黏附。为解释这一现象,我们在此提出一种受限聚合物模型,以研究由聚合物排斥剂和配体 - 受体键介导的分子黏附稳定性。在该模型中,排斥剂和结合剂均被视为限制在纳米狭缝中的蠕虫状链,黏附稳定性被视为配体 - 受体结合的吸引力与排斥剂和结合剂之间尺寸不匹配所产生的排斥力之间的竞争。根据受限聚合物模型计算每个配体 - 受体键上的力,并使用贝尔经典模型描述配体 - 受体键的缔合/解离反应。计算得到的平衡键分布表明,存在稳定黏附的临界配体密度,对应一个临界配体间距,这不仅在定性上而且在定量上与实验观察结果一致。在稳定黏附的情况下,该模型预测黏附表面之间的平衡间距低于配体 - 受体键轮廓长度的60%。

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