Dipartimento di Scienze Chimiche, Università di Catania, Viale A. Doria, 6-95125 Catania, Italy.
J Chem Phys. 2010 Jan 28;132(4):045103. doi: 10.1063/1.3290823.
A semiquantitative theory aimed to describe the adhesion kinetics between soft objects, such as living cells or vesicles, has been developed. When rigid bodies are considered, the adhesion kinetics is successfully described by the classical Derjaguin, Landau, Verwey, and Overbeek (DLVO) picture, where the energy profile of two approaching bodies is given by a two asymmetrical potential wells separated by a barrier. The transition probability from the long-distance to the short-distance minimum defines the adhesion rate. Conversely, soft bodies might follow a different pathway to reach the short-distance minimum: thermally excited fluctuations give rise to local protrusions connecting the approaching bodies. These transient adhesion sites are stabilized by short-range adhesion forces (e.g., ligand-receptor interactions between membranes brought at contact distance), while they are destabilized both by repulsive forces and by the elastic deformation energy. Above a critical area of the contact site, the adhesion forces prevail: the contact site grows in size until the complete adhesion of the two bodies inside a short-distance minimum is attained. This nucleation mechanism has been developed in the framework of a nonequilibrium Fokker-Planck picture by considering both the adhesive patch growth and dissolution processes. In addition, we also investigated the effect of the ligand-receptor pairing kinetics at the adhesion site in the time course of the patch expansion. The ratio between the ligand-receptor pairing kinetics and the expansion rate of the adhesion site is of paramount relevance in determining the overall nucleation rate. The theory enables one to self-consistently include both thermodynamics (energy barrier height) and dynamic (viscosity) parameters, giving rise in some limiting cases to simple analytical formulas. The model could be employed to rationalize fusion kinetics between vesicles, provided the short-range adhesion transition is the rate-limiting step to the whole adhesion process. Approximate relationships between the experimental fusion rates reported in the literature and parameters such as membrane elastic bending modulus, repulsion strength, temperature, osmotic forces, ligand-receptor binding energy, solvent and membrane viscosities are satisfactory explained by our model. The present results hint a possible role of the initial long-distance-->short-distance transition in determining the whole fusion kinetics.
已经开发出一种半定量理论,旨在描述软物体(如活细胞或囊泡)之间的粘附动力学。当考虑刚体时,经典的德贾林格、朗道、维韦和奥弗贝克(DLVO)图像成功地描述了粘附动力学,其中两个接近物体的能量曲线由两个不对称的势阱通过势垒分隔。从远距离到近距离最小值的跃迁概率定义了粘附速率。相反,软体会通过不同的途径到达近距离最小值:热激发的涨落会导致连接接近物体的局部突起。这些瞬态粘附位点由短程粘附力(例如,在接触距离下的膜之间的配体-受体相互作用)稳定,同时它们被排斥力和弹性变形能不稳定化。在接触位点的临界面积之上,粘附力占主导地位:接触位点会增大,直到两个物体在近距离最小值内完全粘附。这种成核机制是在非平衡福克-普朗克图像的框架内发展起来的,同时考虑了粘附斑块的生长和溶解过程。此外,我们还研究了在斑块扩展过程中配体-受体配对动力学在粘附位点上的时间过程中的影响。配体-受体配对动力学与粘附位点扩展速率之间的比值在决定总体成核速率方面至关重要。该理论可以自洽地包括热力学(能垒高度)和动力学(粘度)参数,在某些极限情况下会产生简单的解析公式。该模型可用于合理化囊泡之间的融合动力学,前提是短程粘附转变是整个粘附过程的限速步骤。通过我们的模型,可以很好地解释文献中报道的实验融合速率与膜弹性弯曲模量、排斥强度、温度、渗透压、配体-受体结合能、溶剂和膜粘度等参数之间的近似关系。目前的结果表明,初始远距离-近距离转变可能在决定整个融合动力学中起作用。