Department of Physics, Graduate School of Science, Tohoku University , 6-3, Aramaki Aza-Aoba, Aoba-ku, Sendai 980-8578, Japan.
Laboratoire Matière et Systèmes Complexes, Universitè Paris Diderot (Paris 7) , F-75205 Paris Cedex 13, France.
Langmuir. 2017 Oct 10;33(40):10698-10706. doi: 10.1021/acs.langmuir.7b02617. Epub 2017 Sep 26.
We have investigated the migrations of phospholipid vesicles under the concentration gradients of metal ions. We microinjected metal chloride solutions, monovalent (NaCl and KCl), divalent (CaCl and MgCl), and trivalent (LaCl) salts, toward phospholipid giant vesicles (GVs) composed of 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC). For NaCl, CaCl, and MgCl solutions, the GVs migrated straight toward the tip of the micropipette in response to the concentration gradients, whereas for KCl and LaCl, GVs moved to the opposite direction. Our motion tracking of lipid domains in a vesicle membrane showed no unidirectional flow in the membrane during the vesicle migration, indicating that the Marangoni mechanism is not responsible for the observed vesicle migration. We calculated the diffusiophoretic velocities for symmetric and asymmetrical electrolytes by solving the Stokes' equation numerically. The theoretical diffusiophoretic velocities described the observed migration velocities well. Thus, we can control the migration of vesicle in response to the concentration gradient by adapting the electrolytes and the lipids.
我们研究了磷脂囊泡在金属离子浓度梯度下的迁移。我们向由 1,2-二油酰基-sn-甘油-3-磷酸胆碱 (DOPC) 组成的巨大磷脂囊泡 (GV) 微注射金属氯化物溶液,包括单价 (NaCl 和 KCl)、二价 (CaCl 和 MgCl) 和三价 (LaCl) 盐。对于 NaCl、CaCl 和 MgCl 溶液,GV 响应浓度梯度直接向微管尖端迁移,而对于 KCl 和 LaCl,GV 则向相反方向迁移。我们对囊泡膜中脂质域的运动追踪显示,在囊泡迁移过程中膜内没有单向流动,表明 Marangoni 机制不是囊泡迁移的原因。我们通过数值求解 Stokes 方程计算了对称和非对称电解质的扩散泳速度。理论扩散泳速度很好地描述了观察到的迁移速度。因此,我们可以通过适应电解质和脂质来控制囊泡的迁移以响应浓度梯度。