Department of Chemical and Biomolecular Engineering, University of Pennsylvania , 220 South 33rd Street, 311A Towne Building, Philadelphia, Pennsylvania 19104, United States.
Department of Bioengineering, University of Pennsylvania , 210 South 33rd St., 240 Skirkanich Hall, Philadelphia, Pennsylvania 19104, United States.
Langmuir. 2017 Jan 17;33(2):600-610. doi: 10.1021/acs.langmuir.6b03406. Epub 2016 Dec 30.
Inspired by proteins that generate membrane curvature, sense the underlying membrane geometry, and migrate driven by curvature gradients, we explore the question: Can colloids, adhered to lipid bilayers, also sense and respond to membrane geometry? We report the migration of Janus microparticles adhered to giant unilamellar vesicles elongated to present spatially varying curvatures. In our experiments, colloids migrate only when the membranes are tense, suggesting that they migrate to minimize membrane area. By determining the energy dissipated along a trajectory, the energy field is inferred to depend on the local deviatoric curvature, like curvature driven capillary migration on interfaces between immiscible fluids. In this latter system, energy gradients are larger, so colloids move deterministically, whereas the paths traced by colloids on vesicles have significant fluctuations. By addressing the role of Brownian motion, we show that the observed migration is analogous to curvature driven capillary migration, with membrane tension playing the role of interfacial tension. Since this motion is mediated by membrane shape, it can be turned on and off by dynamically deforming the vesicle. While particle-particle interactions on lipid membranes have been considered in many contributions, we report here an exciting and previously unexplored modality to actively direct the migration of colloids to desired locations on lipid bilayers.
受能够产生膜曲率、感知基底膜几何形状并在曲率梯度驱动下迁移的蛋白质的启发,我们探讨了这样一个问题:胶体黏附在脂质双层膜上,是否也能感知和响应膜的几何形状?我们报告了黏附在巨大的单分子层囊泡上的各向异性微颗粒在囊泡被拉伸以呈现出空间变化的曲率时的迁移行为。在我们的实验中,胶体只有在膜紧张时才会迁移,这表明它们迁移是为了最小化膜面积。通过确定轨迹上耗散的能量,可以推断出能量场取决于局部的偏曲曲率,就像在不混溶流体界面上的曲率驱动毛细迁移一样。在后一种系统中,能量梯度更大,因此胶体可以确定性地移动,而胶体在囊泡上的轨迹则有很大的波动。通过解决布朗运动的作用,我们表明观察到的迁移类似于曲率驱动的毛细迁移,膜张力起着界面张力的作用。由于这种运动是由膜形状介导的,因此可以通过动态变形囊泡来开启和关闭。虽然在许多贡献中已经考虑了脂质膜上的粒子间相互作用,但我们在这里报告了一种令人兴奋的、以前未被探索的模式,可以主动将胶体引导到脂质双层上所需的位置。