Department of Biomedical Engineering, University of Rochester, Medical Center, Rochester, New York, USA.
Biophys J. 2009 Jan;96(1):268-75. doi: 10.1016/j.bpj.2008.09.009.
The formation of receptor ligand bonds at the interface between different cells and between cells and substrates is a widespread phenomenon in biological systems. Physical measurements of bond formation rates between cells and substrates have been exploited to increase our understanding of the biophysical mechanisms that regulate bond formation at interfaces. Heretofore, these measurements have been interpreted in terms of simple bimolecular reaction kinetics. Discrepancies between this simple framework and the behavior of neutrophils adhering to surfaces expressing vascular cell adhesion molecule 1 (VCAM-1) motivated the development of a new kinetic framework in which the explicit formation of active bond formation sites (reaction zones) are a prerequisite for bond formation to occur. Measurements of cells interacting with surfaces having a wide range of VCAM-1 concentrations, and for different durations of contact, enabled the determination of novel kinetic rate constants for the formation of reaction zones and for the intrinsic bond kinetics. Comparison of these rates with rates determined previously for other receptor-ligand pairs points to a predominant role of extrinsic factors such as surface topography and accessibility of active molecules to regions of close contact in determining forward rates of bond formation at cell interfaces.
不同细胞之间以及细胞与基底之间的受体配体键的形成是生物系统中广泛存在的现象。细胞与基底之间键形成速率的物理测量已被用于加深我们对调节界面键形成的生物物理机制的理解。迄今为止,这些测量结果是根据简单的双分子反应动力学来解释的。这种简单框架与粘附在表达血管细胞黏附分子 1 (VCAM-1)的表面上的中性粒细胞的行为之间的差异促使开发了一种新的动力学框架,其中明确形成活性键形成位点(反应区)是键形成发生的前提。对与具有广泛 VCAM-1 浓度的表面相互作用的细胞进行测量,并接触不同的时间,可以确定反应区形成和固有键动力学的新的动力学速率常数。将这些速率与先前为其他受体-配体对确定的速率进行比较,表明在确定细胞界面处键形成的正向速率时,表面形貌和活性分子与紧密接触区域的可及性等外在因素起着主要作用。