Vesicle adhesion in flow

IF 2.6 4区 物理与天体物理 Q4 CHEMISTRY, PHYSICAL
Lucia Wesenberg, Felix Weissenfeld, Kai-Uwe Hollborn, Motomu Tanaka, Marcus Müller
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Abstract

The dynamic adhesion of lipid vesicles in shear flow is governed by the interplay of membrane-bending rigidity, membrane–substrate adhesion energy, and hydrodynamic stresses. While the equilibrium contact curvature is determined by the transversality condition, shear flow can additionally deform the adhered vesicle, drive translational motion, or, through hydrodynamic lift forces, promote detachment of the vesicle from the substrate. Here, we investigate adhered vesicles in shear flow subjected to a reversible change of the membrane-wall interactions. Using a stimuli-responsive poly(acrylic acid-co-cysteine) brush, whose adhesive properties are modulated by the controlled addition and removal of Cd\(^{2+}\) ions, and using reflection interference contrast microscopy, we track the membrane–substrate separation and vesicle shape throughout the transition. Using molecular dynamics simulations within the Helfrich framework, we provide microscopic insights into the deformation processes and systematically investigate the dependence on the shear-flow strength. Two parameters govern the dynamic response: (i) the balance between adhesion and membrane bending, and (ii) the ratio between viscous shear and bending stresses. In the strong-adhesion regime, a large rim of the contact zone between membrane and substrate and an increased density of wall springs lead to a significant increase in wall springs that must rupture per unit displacement. This effectively suppresses tank-treading motion. Reducing adhesion decreases the contact-zone rim and wall-spring density, enabling flow-driven translational transport. Simultaneously, shear flow induces a shape asymmetry, manifested as a forward tilt of the vesicle. As a consequence, the curvature at the preceding edge decreases, whereas the curvature at the receding edge increases. These results demonstrate that vesicle motion on polymer-brush-coated substrates can be reversibly controlled by chemical stimuli, providing a tunable platform to study adhesion dynamics under flow.

流动中的囊泡粘连。
剪切流中脂质囊泡的动态粘附受膜弯曲刚度、膜-基质粘附能和流体动力应力的相互作用控制。而平衡接触曲率是由横向条件决定的,剪切流动还可以使粘附的囊泡变形,驱动平移运动,或者通过流体动力升力促进囊泡从基质上脱离。在这里,我们研究了剪切流中受膜-壁相互作用可逆变化的粘附囊泡。使用刺激响应的聚丙烯酸-共半胱氨酸刷,其粘附性能通过控制cd2 +离子的添加和去除来调节,并使用反射干涉对比显微镜,我们在整个过渡过程中跟踪膜-底物分离和囊泡形状。利用helrich框架内的分子动力学模拟,我们提供了对变形过程的微观洞察,并系统地研究了剪切流强度对变形过程的依赖。控制动态响应的两个参数是:(i)粘附力和膜弯曲之间的平衡,以及(ii)粘性剪切应力和弯曲应力之间的比率。在强粘附状态下,膜和基材之间接触区的较大边缘以及壁弹簧密度的增加导致每单位位移必须破裂的壁弹簧显著增加。这有效地抑制了坦克履带运动。减少黏附会降低接触区边缘和壁面弹簧密度,从而实现流动驱动的平移输送。同时,剪切流动引起形状不对称,表现为囊泡向前倾斜。结果,前边缘的曲率减小,而后边缘的曲率增大。这些结果表明,化学刺激可以可逆地控制聚合物刷涂基底上的囊泡运动,为研究流动下的粘附动力学提供了一个可调的平台。
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来源期刊
The European Physical Journal E
The European Physical Journal E CHEMISTRY, PHYSICAL-MATERIALS SCIENCE, MULTIDISCIPLINARY
CiteScore
2.60
自引率
5.60%
发文量
92
审稿时长
3 months
期刊介绍: EPJ E publishes papers describing advances in the understanding of physical aspects of Soft, Liquid and Living Systems. Soft matter is a generic term for a large group of condensed, often heterogeneous systems -- often also called complex fluids -- that display a large response to weak external perturbations and that possess properties governed by slow internal dynamics. Flowing matter refers to all systems that can actually flow, from simple to multiphase liquids, from foams to granular matter. Living matter concerns the new physics that emerges from novel insights into the properties and behaviours of living systems. Furthermore, it aims at developing new concepts and quantitative approaches for the study of biological phenomena. Approaches from soft matter physics and statistical physics play a key role in this research. The journal includes reports of experimental, computational and theoretical studies and appeals to the broad interdisciplinary communities including physics, chemistry, biology, mathematics and materials science.
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