Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Mechanisms of Membrane Domain Formation00:59

Mechanisms of Membrane Domain Formation

2.9K
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...
2.9K
Membrane Domains01:18

Membrane Domains

5.3K
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...
5.3K
Membrane Fluidity01:23

Membrane Fluidity

150.3K
Cell membranes are composed of phospholipids, proteins, and carbohydrates loosely attached to one another through chemical interactions. Molecules are generally able to move about in the plane of the membrane, giving the membrane its flexible nature called fluidity. Two other features of the membrane contribute to membrane fluidity: the chemical structure of the phospholipids and the presence of cholesterol in the membrane.
150.3K
Fluid Mosaic Model01:19

Fluid Mosaic Model

11.2K
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...
11.2K
Detergent Purification of Membrane Proteins01:18

Detergent Purification of Membrane Proteins

5.0K
Detergents are used to purify the integral proteins of the membrane. The hydrophobic portion of the detergent can replace membrane phospholipids while solubilizing the membrane proteins. When detergent monomers reach a specific concentration in a solution called critical micelle concentration (CMC), they form micelles. Above CMC, the concentration of the detergent monomers remains in equilibrium with the micelle. The number of detergent monomers present in the CMC varies for each detergent, and...
5.0K
The Fluid Mosaic Model01:34

The Fluid Mosaic Model

142.4K
The fluid mosaic model was first proposed as a visual representation of research observations. The model comprises the composition and dynamics of membranes and serves as a foundation for future membrane-related studies. The model depicts the structure of the plasma membrane with a variety of components, which include phospholipids, proteins, and carbohydrates. These integral molecules are loosely bound, defining the cell’s border and providing fluidity for optimal function.
142.4K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Engineering Ultrathin Bismuth Nanosheets With Active Facet for Highly Efficient CO<sub>2</sub> Electroreduction to Formate.

ChemSusChem·2026
Same author

Long-cycling organic flow batteries enabled by electronic-spatial synergistic modulation.

Science advances·2026
Same author

Manipulating cation solvation equilibrium in sole-solvent electrolyte for fast-charging and wide-temperature-range sodium metal batteries.

Nature communications·2026
Same author

Author Correction: Solution-sheared supramolecular oligomers with enhanced thermal resistance in interfacial adhesion and bulk cohesion.

Nature communications·2026
Same author

Bioinspired Ultrafast All-Climate Self-Charging Flow Battery.

ACS applied materials & interfaces·2026
Same author

Rational Design of Nanostructured Ionic Conductive Polymer Organogels for Ultrasensitive Flexible Styrene Sensor.

ACS sensors·2026

相关实验视频

Updated: May 17, 2025

Transmembrane Domain Oligomerization Propensity determined by ToxR Assay
06:45

Transmembrane Domain Oligomerization Propensity determined by ToxR Assay

Published on: May 26, 2011

15.2K

精确的寡合体组织增强了静电相互作用,以有效地结合细胞膜.

Yuanyuan Zhao1, Yiqian Luo2, Yi Chai3

  • 1School of Fashion and Textiles, The Hong Kong Polytechnic University, Hong Kong 999077, China.

Nano letters
|May 16, 2025
PubMed
概括
此摘要是机器生成的。

定向聚化寡合物增强了它们与细胞膜的静电相互作用,显著改善了用于生物医学应用的纳米材料细胞捕获. 这种分子导向控制加速了细菌细胞膜的结合和破坏.

关键词:
在RAFT的聚合物化过程中,抗菌表面是一种抗菌表面.静电相互作用 静电相互作用这是一种机械杀菌剂.氧化纳米棒的使用方法

更多相关视频

Cellular Affinity of Particle-Stabilized Emulsion to Boost Antigen Internalization
10:06

Cellular Affinity of Particle-Stabilized Emulsion to Boost Antigen Internalization

Published on: September 2, 2022

1.7K
Native Cell Membrane Nanoparticles System for Membrane Protein-Protein Interaction Analysis
07:31

Native Cell Membrane Nanoparticles System for Membrane Protein-Protein Interaction Analysis

Published on: July 16, 2020

5.9K

相关实验视频

Last Updated: May 17, 2025

Transmembrane Domain Oligomerization Propensity determined by ToxR Assay
06:45

Transmembrane Domain Oligomerization Propensity determined by ToxR Assay

Published on: May 26, 2011

15.2K
Cellular Affinity of Particle-Stabilized Emulsion to Boost Antigen Internalization
10:06

Cellular Affinity of Particle-Stabilized Emulsion to Boost Antigen Internalization

Published on: September 2, 2022

1.7K
Native Cell Membrane Nanoparticles System for Membrane Protein-Protein Interaction Analysis
07:31

Native Cell Membrane Nanoparticles System for Membrane Protein-Protein Interaction Analysis

Published on: July 16, 2020

5.9K

科学领域:

  • 生物材料科学 生物材料科学
  • 纳米技术 纳米技术
  • 细胞工程 细胞工程

背景情况:

  • 有效地将细胞膜与纳米材料结合,对于先进的生物医学应用至关重要.
  • 目前的方法往往缺乏精确控制纳米材料-细胞相互作用.

研究的目的:

  • 为了研究控制的寡合体导向如何影响细胞膜与纳米材料的结合.
  • 开发一种增强纳米材料-细胞静电相互作用的方法.

主要方法:

  • 使用可逆添加-碎片化链转移 (RAFT) 聚合物合成的聚化寡合物,具有伊米达头和尾.
  • 通过头对头 π-π 相互作用研究了寡合体的自我组装.
  • 评估了面向与未经修改的纳米结构的细胞膜捕获效率和杀死细菌率.

主要成果:

  • 面向的寡合体显示出与负电荷细胞膜显著增强的静电相互作用.
  • 细胞膜捕获通过面向的寡合体的空间排列明显加速.
  • 使用面向寡合体,杀死细菌的时间从100分钟缩短到3分钟.

结论:

  • 精细控制聚化寡合体中的分子导向,增强对细胞膜的静电吸引力.
  • 这种方法为改善诊断和细胞工程中的纳米材料-细胞相互作用提供了一个有希望的策略.
  • 分子导向是优化生物系统中生物材料性能的一个关键因素.