活性囊泡的变形诱导的相位分离.
Yi-Yang Jin1, Yan Jin1, Zi-Xuan Shi1
1Center for Soft Condensed Matter Physics & Interdisciplinary Research, School of Physical Science and Technology, Soochow University, Suzhou 215006, China. kangchen@suda.edu.cn.
Physical chemistry chemical physics : PCCP
|September 16, 2024
概括
当它们的可变形活性发生变化时,可变形活性囊泡 (DAVs) 呈现相位分离. 这个活性物质模型显示了气体,液体和固体状态之间的过渡,影响了集体行为.
科学领域:
- 物理 物理学 物理
- 软物质物理学 软物质物理学
- 生物物理学的生物物理.
背景情况:
- 细胞和细菌等活性物质本质上是可变形的.
- 变形性在复杂环境中的活性物质的集体行为和运动中起着至关重要的作用.
研究的目的:
- 引入和研究一个二维可变形活性囊泡 (DAV) 模型来模拟类似细胞的可变形活性物质.
- 探索可调整的可变形性如何影响活性物质的集体行为和相位过渡.
主要方法:
- 开发一个二维可变形活性囊泡 (DAV) 模型.
- 持续调整粒子变形性以观察系统反应.
- 分析相变,有效度,粒子大小和形状,运动性和应力.
主要成果:
- 变形能力的变化会导致DAV的相位分离.
- 系统在同质气体,气液共存和气体固体共存状态之间进行过渡.
- 由变形引起的相分离与有效度,颗粒大小和形状的非单调变化有关.
- 变形性会影响分离后的密度阶段内的运动性和应力.
结论:
- 变形性是一个关键参数,它决定了活性物质的集体行为和新兴性质.
- DAV模型为研究可变形性对活性物质系统的影响提供了一个平台.
- 这些发现为生物和合成活性物质的自我组织和新兴现象提供了新的见解.
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
Vesicular Tubular Clusters
2.5K
After budding out from the ER membrane, some COPII vesicles lose their coat and fuse with one another to form larger vesicles and interconnected tubules called vesicular tubular clusters or VTCs. These clusters constitute a compartment at the ER-Golgi interface known as ERGIC (Endoplasmic Reticulum Golgi Intermediate Compartment). The ERGIC is a mobile membrane-bound cargo transport system that sorts proteins secreted from ER and delivers them to the Golgi.
With the help of motor proteins such...
With the help of motor proteins such...
2.5K
SNAREs and Membrane Fusion
10.8K
Once a transport vesicle has recognized its target organelle, the vesicular membrane needs to fuse with the target membrane to unload the cargo. Transmembrane proteins called SNAREs present on organelle membranes and their vesicles, mediate vesicle fusion.
SNAREs exist in pairs that symmetrically interact and catalyze the fusion of the lipid bilayers in vesicle and target organelle. v-SNARE in the vesicle membrane are single polypeptide chains that bind to a complementary t-SNARE, composed of 2...
SNAREs exist in pairs that symmetrically interact and catalyze the fusion of the lipid bilayers in vesicle and target organelle. v-SNARE in the vesicle membrane are single polypeptide chains that bind to a complementary t-SNARE, composed of 2...
10.8K
Fusion of Secretory Vesicles with the Plasma Membrane
11.0K
Proteins and neurotransmitters in secretory vesicles can be released from a cell upon vesicle docking, priming, and fusion with the plasma membrane. Vesicles are docked and primed in preparation for the quick exocytosis of their contents in response to a stimulus. The fusion process is mainly carried out by a SNAP Receptor or SNARE complex, consisting of synaptobrevin, syntaxin-1, and SNAP-25.
In 1993, Jim Rothman proposed that the antiparallel pairing of vesicular and transmembrane SNAREs, or...
In 1993, Jim Rothman proposed that the antiparallel pairing of vesicular and transmembrane SNAREs, or...
11.0K
Overview of Secretory Vesicles
8.5K
Secretory vesicles, also known as dense core vesicles (DCVs), are membrane-bound vesicles that transport secretory proteins, such as hormones or neurotransmitters. Regulated secretory vesicles transport proteins from the trans-Golgi network to the exterior of the cell. Proteins present in regulated secretory vesicles are required to be rapidly exocytosed in large amounts upon a specific stimulus.
Various proteins regulate the aggregation of molecules inside the secretory vesicles. Chromogranins...
Various proteins regulate the aggregation of molecules inside the secretory vesicles. Chromogranins...
8.5K
Cell Motility through Blebbing
1.9K
Blebs are a type of membrane protrusion formed by the internal hydrostatic pressure of the cytoplasm. Blebs are observed in several cell types, including fibroblasts, immune cells, and single-celled organisms like the amoeba. The primary function of blebs is cell locomotion and apoptosis, but they are also found during necrosis and cell division. The life cycle of a bleb comprises an initiation phase followed by the expansion and retraction phases.
Blebbing Through the Matrix
In multicellular...
Blebbing Through the Matrix
In multicellular...
1.9K


