Studying receptor-mediated cell adhesion at the single molecule level.

A Pierres, A M Benoliel, P Bongrand
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引用次数: 38

Abstract

Cell adhesion is essentially mediated by specific interactions between membrane receptors and ligands. It is now apparent that the mere knowledge of the on- and off-rate of association of soluble forms of these receptors and ligands is not sufficient to yield accurate prediction of cell adhesive behavior. During the last few years, a variety of complementary techniques relying on the use of hydrodynamic flow, atomic force microscopy, surface forces apparatus or soft vesicles yielded accurate information on i) the dependence of the lifetime of individual bonds on applied forces and ii) the distance dependence of the association rate of bound receptors and ligands. The purpose of this review is, first to recall the physical significance of these parameters, and second to describe newly obtained results. It is emphasized that molecular size and flexibility may be a major determinant of the efficiency of receptor mediated adhesion, and this cannot be studied by conventional methods dealing with soluble molecules.

在单分子水平上研究受体介导的细胞粘附。
细胞粘附本质上是由膜受体和配体之间的特异性相互作用介导的。现在很明显,仅仅了解这些受体和配体的可溶性形式的结合的开断率是不足以准确预测细胞粘附行为的。在过去的几年里,依靠流体动力学流动、原子力显微镜、表面力仪器或软囊的各种互补技术,获得了以下方面的准确信息:1)单个键的寿命对施加力的依赖;2)结合受体和配体的结合率对距离的依赖。这篇综述的目的是,首先回顾这些参数的物理意义,其次描述新获得的结果。强调分子大小和柔韧性可能是受体介导的粘附效率的主要决定因素,这不能通过处理可溶性分子的传统方法来研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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