病毒颗粒的自发双层包裹由脂兰格穆尔单层包裹
J F Torres-Salgado1, M V Villagrana-Escareño1, A L Duran-Meza1,2
1Biological Physics Laboratory, Institute of Physics, Universidad Autónoma de San Luis Potosí, San Luis/dF Potosí, 78000, San Luis Potosí, México.
The European physical journal. E, Soft matter
|December 5, 2023
概括
裸露牛的性斑点病毒 (CCMV) 颗粒自发获得的脂质双层包裹,当注射到含有混合脂质单层的Langmuir中时. 这一发现揭示了由静电相互作用驱动的病毒颗粒修饰的新机制.
科学领域:
- 生物物理学的生物物理.
- 材料科学 材料科学 材料科学
- 病毒学 病毒学
背景情况:
- 牛类性斑点病毒 (CCMV) 是一种特征很好,负电荷的病毒.
- 兰木尔谷被用来研究空气-水接口上的脂质单层.
- 阴离子脂质可以与阴离子生物结构相互作用.
研究的目的:
- 为了研究CCMV颗粒与混合脂质单层之间的自发相互作用.
- 为了确定病毒颗粒是否可以获得脂质包裹.
- 阐明病毒-脂质相互作用的机制.
主要方法:
- 将"裸体"CCMV颗粒注入Langmuir沟的子相中.
- 在空气-水界面形成混合脂质单层 (DMPC:CTAB).
- 监测表面压力变化和脂质去除.
- 使用原子力显微镜对被包裹的病毒颗粒进行表征.
主要成果:
- CCMV粒子自发获得的脂质双层包裹.
- 表面压力随着脂质从接口中去除而显著下降.
- 原子力显微镜证实了病毒颗粒周围存在脂质双层.
- 该过程涉及初始单层吸附,随后形成双层.
结论:
- 静电相互作用和热波动驱动了阴离子CCMV由阴离子脂质的自发包裹.
- 病毒颗粒可以通过与充电的脂质单层相互作用来获得脂质包裹.
- 这项研究展示了一种用于病毒颗粒功能化的新方法.
相关概念视频
Asymmetric Lipid Bilayer
7.3K
Biological membranes show uneven distribution of different types of lipids in the inner and outer layers, resulting in transverse asymmetric membranes. The treatment of the erythrocyte membrane with the enzyme phospholipase confirmed the asymmetric nature of the lipid bilayer. The enzyme hydrolyzes lipids into fatty acids and hydrophilic groups. The phospholipase acts only on the outer layer of the membrane, while the inner layer remains intact. The phospholipase treatment resulted in 80%...
7.3K
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
Lytic Cycle of Bacteriophages
70.8K
Bacteriophages, also known as phages, are specialized viruses that infect bacteria. A key characteristic of phages is their distinctive “head-tail” morphology. A phage begins the infection process (i.e., lytic cycle) by attaching to the outside of a bacterial cell. Attachment is accomplished via proteins in the phage tail that bind to specific receptor proteins on the outer surface of the bacterium. The tail injects the phage’s DNA genome into the bacterial cytoplasm. In the...
70.8K
Fluid Mosaic Model
11.9K
Scientists identified the plasma membrane in the 1890s and its principal chemical components (lipids and proteins) by 1915. The model for plasma membrane structure, proposed in 1935 by Hugh Davson and James Danielli, was the first model to be widely accepted in the scientific community. The model was based on the plasma membrane's "railroad track" appearance in early electron micrographs. Davson and Danielli theorized that the plasma membrane's structure resembled a sandwich...
11.9K
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


