引发钉的微滴子自我运输
Hyeongyun Cha1,2,3, Moon-Kyung Kim1, Ho Chan Chang1
1Department of Mechanical Science and Engineering, University of Illinois Urbana-Champaign, Urbana, Illinois 61801, United States.
ACS nano
|March 13, 2025
概括
表面缺陷可能会导致微滴粘附. 然而,设计的表面异质性使微滴能够在没有外力的情况下自我运输,利用固定效应来实现自发运动.
科学领域:
- 物理 物理学 物理
- 材料科学 材料科学 材料科学
- 表面科学是一门学科.
背景情况:
- 微滴由于不可避免的微和纳米尺度缺陷而粘附于固体表面.
- 表面和潜在能量梯度或外部能量通常需要启动滴滴运动.
研究的目的:
- 为了证明设计的表面异质性可以诱导自发的微滴自我运输.
- 探索一种没有外力或异构的液滴移动的替代机制.
主要方法:
- 研究拓缺陷对微滴状物行为的影响.
- 分析接触线钉定位及其在产生不对称性的作用.
主要成果:
- 微滴在远远超过其半径 (10-20倍) 的距离上表现出自发运动.
- 接触线在拓缺陷上固定导致接触角不对称,驱动运动.
- 自传发生在没有外部能量输入或固有的表面异构性的情况下.
结论:
- 表面异质性,当适当设计时,可以用于被动滴水流动.
- 这一发现为控制需要被动运输的应用中滴滴运动提供了一种新的方法.
相关概念视频
Pinching-off of Coated Vesicles
3.1K
Vesicle budding is orchestrated by distinct cytosolic proteins such as adaptor proteins, coat proteins, and GTPases. To initiate vesicle budding, membrane-bending proteins containing crescent-shaped BAR domains bind to the lipid heads in the bilayer and distort the membrane to form a protein-coated vesicle bud. Adaptors proteins such as AP2 for clathrin-coated vesicles can nucleate on the deformed membrane. Finally, coat proteins such as clathrin or COPI and COPII assemble into a coat forming...
3.1K
Mechanism of Lamellipodia Formation
2.5K
Cells migrating in response to external stimuli form lamellipodia, which are thin membrane protrusions supported by a mesh of linked, branched, or unbranched actin filaments. These actin filaments interact with myosin motor proteins, creating the dynamic actomyosin complex within the cytoskeleton. Contractility, or the ability to generate contractile stress, is inherent to the actomyosin complex. It helps cells detect the stiffness of the surrounding ECM and exert contractile force for...
2.5K


