原子主义的洞察力 纳领域的脂质的突触囊泡
Christopher Kang1, Kazuumi Fujioka1, Rui Sun1
1Department of Chemistry, The University of Hawai'i, Ma̅noa, 2545 McCarthy Mall, Honolulu, Hawaii 96822, United States.
The journal of physical chemistry. B
|February 7, 2024
概括
膜曲率积极塑造细胞膜,在突触囊泡中诱导脂质纳米域. 这一发现表明,曲率驱动了相位分离,否则会破坏膜的秩序.
科学领域:
- 生物物理学的生物物理.
- 细胞生物学 细胞生物学
- 神经科学是一个神经科学.
背景情况:
- 膜曲率在历史上被认为是被动的,但积极调节膜性质.
- 曲率可以导致膜成分的分离,形成生物相关的纳米域.
- 与神经退行相关的蛋白质对突触囊泡表现出亲和力,而突触囊泡缺乏明显的有序纳米领域.
研究的目的:
- 为了研究现实的高斯曲率对突触囊泡膜动态的影响.
- 为了确定膜曲率是否影响突触囊泡内的脂质纳米域组织.
- 探索曲率在诱导神经元膜相位分离中的作用.
主要方法:
- 使用了全原子分子动力学模拟.
- 模拟了一个全尺寸的突触囊泡,具有现实的高斯曲率.
- 分析了膜动力学,脂质纳米域组织,每脂质的表面积,顺序参数和域寿命.
主要成果:
- 在突触囊泡膜中确定了纳米领域形成的令人信服的指标.
- 与平面双层相比,观察到的组成,每脂质表面积,顺序参数和域寿命的差异.
- 证明曲率会诱导脂质纳米域组织,而这种组织在平面膜中不存在.
结论:
- 膜曲率积极诱导脂质纳米域的形成和组织在突触囊泡.
- 曲率在神经元膜内的驱动阶段分离中起着至关重要的作用.
- 这种机制可以解释与突触囊泡中神经退行相关的蛋白质的行为.
相关概念视频
Membrane Domains
5.4K
The membrane domains concentrate specific lipids and proteins at one place within the membrane, which helps in cell signaling, adhesion, and other critical cellular processes. These domains can differ in size, composition, function, and lifespan.
Protein Domains
The membrane comprises a group of distinct proteins responsible for carrying out a cell's specific function. For example, the plasma membrane of the human sperm, or a single germ cell, contains a unique set of proteins in the...
Protein Domains
The membrane comprises a group of distinct proteins responsible for carrying out a cell's specific function. For example, the plasma membrane of the human sperm, or a single germ cell, contains a unique set of proteins in the...
5.4K
Mechanisms of Membrane Domain Formation
3.0K
Different physical properties of lipids and proteins allow them to localize and form distinct islands or domains in the membrane. Some membrane domains are formed due to protein-protein interactions, whereas others are formed due to the presence of specific lipids such as sphingolipids and sterols—for example, large proteins, such as bacteriorhodopsin, aggregate and create distinct domains.
Another mechanism for membrane domain formation involves membrane proteins interacting with...
Another mechanism for membrane domain formation involves membrane proteins interacting with...
3.0K
Fusion of Secretory Vesicles with the Plasma Membrane
11.1K
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...
11.1K
SNAREs and Membrane Fusion
10.9K
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...
10.9K
Pinching-off of Coated Vesicles
3.2K
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...
3.2K
Intralumenal Vesicles and Multivesicular Bodies
3.5K
Intraluminal vesicles (ILVs) are small vesicles 50-80 nm in diameter formed during the maturation of early endosomes. A specialized endosome containing numerous ILVs is called a multivesicular body (MVB). ILVs contain internalized molecules such as antigens, nucleic acids, proteins, and metabolites. Some of these molecules are released from the MVBs inside exosomes and are transported to other cells. Other MVBs contain molecules that are retained in the ILVs and are later degraded within the...
3.5K


