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

Development of Antibiotic Resistance01:30

Development of Antibiotic Resistance

242
Antibiotic resistance is a major public health concern that arises when bacteria evolve mechanisms to withstand the effects of antibiotic treatments. This resistance can be intrinsic, acquired through genetic mutations, or transferred between bacteria via horizontal gene transfer. The development of antibiotic resistance poses significant challenges in treating bacterial infections and necessitates ongoing research to develop new therapeutic strategies.Intrinsic resistance occurs when bacterial...
242
Cellular Membranes and Drug Transport01:24

Cellular Membranes and Drug Transport

998
Drugs must traverse multiple biological barriers, such as multi-layered skin, single-layered intestinal epithelium, and the plasma membrane, to reach their target sites within the body. The plasma membrane, a highly structured composite of phospholipids, carbohydrates, and proteins, is the cell's protective boundary, facilitating selective substance exchange.
Phospholipids arrange themselves into a bilayer, with hydrophilic heads oriented outward and hydrophobic tails facing inward.
998
Pore Transport and Ion-Pair Transport01:17

Pore Transport and Ion-Pair Transport

664
Pore transport and ion-pair formation are critical mechanisms for the absorption and distribution of drugs in the body.
Pore transport, also known as convective transport, is a process where small molecules like urea, water, and sugars rapidly cross cell membranes as though there were channels or pores in the membrane. Although direct microscopic evidence is limited  but the concept of pores or channels is widely accepted based on physiological evidence. Despite the lack of direct...
664
Mechanisms of Drug Absorption: Paracellular, Transcellular, and Vesicular Transport01:23

Mechanisms of Drug Absorption: Paracellular, Transcellular, and Vesicular Transport

861
Drugs need to permeate cell membranes to reach their target sites after administration. Orally administered drugs must transcend intestinal epithelial membrane barriers to infiltrate the systemic circulation. Drugs with a molecular weight of less than 500 Daltons diffuse through gaps between neighboring cells, called paracellular pathways.
However, most drugs use the transcellular route, traversing directly through the cell membranes via two mechanisms: passive and active transport. Passive...
861
Carrier-Mediated Transport01:06

Carrier-Mediated Transport

559
Carrier-mediated transport is a pivotal process in drug absorption, particularly for lipid-insoluble drugs, and encompasses facilitated diffusion and active transport. Facilitated diffusion allows drugs to move along their concentration gradient without energy expenditure, while active transport utilizes ATP to drive drug movement against this gradient.
Active transport involves two types of membrane-spanning transporters: uptake and efflux. Uptake transporters are expressed in the small...
559
Surface Membrane Barriers01:18

Surface Membrane Barriers

1.5K
The skin and mucous membranes serve as the primary line of defense against pathogens by providing both physical and chemical protection. These barriers are essential in preventing the entry and establishment of microbes, thereby maintaining the integrity of the host.
The outer layer of the skin, the epidermis, is a robust barrier comprising layers of closely packed keratinized cells. This dense arrangement prevents microbes from penetrating the body. The periodic shedding of epidermal cells...
1.5K

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

<i>ag85A</i> loss promotes free mycolate accumulation and sensitizes plasma membrane domain to disruption.

Journal of bacteriology·2026
Same author

Identification of chemical features for improved outer membrane permeation in mycobacteria using machine learning.

Nature microbiology·2026
Same author

Loss of essential outer membrane functions causes drug hypersensitization in <i>Acinetobacter baumannii</i> overexpressing multidrug efflux pumps.

mBio·2026
Same author

Rifamycin Structural Modifications Attenuate PXR Binding and CYP3A4 Induction.

Journal of medicinal chemistry·2026
Same author

<i>Escherichia coli</i> and Mammalian Cells Follow Divergent Rules for Lipid-Driven Cytosolic Accumulation.

bioRxiv : the preprint server for biology·2026
Same author

'No lu'au for baby's 1st birthday': becoming a mother during the COVID-19 pandemic in Hawai'i.

Ethnicity & health·2026

相关实验视频

Updated: Sep 19, 2025

In vitro Investigation of the MexAB Efflux Pump From Pseudomonas aeruginosa
13:40

In vitro Investigation of the MexAB Efflux Pump From Pseudomonas aeruginosa

Published on: February 17, 2014

12.0K

菌膜不同且异质地限制了抗生素透.

Irene Lepori1, Kiserian Jackson1,2, Zichen Liu3,4

  • 1Department of Microbiology, University of Massachusetts, Amherst, Massachusetts 01003, United States.

ACS infectious diseases
|June 5, 2025
PubMed
概括

菌根菌外膜选择性地阻止抗生素进入,作为细胞特异性屏障. 这一发现,使用Peptidoglycan可访问性点击介导评估 (PAC-MAN) 方法,揭示了Mycobacterium结核病中药物透的差异.

关键词:
抗生素 抗生素是一种抗生素.生物对角点击化学细胞外的细胞外.透性 透性的结核病是一种肺结核病.

更多相关视频

Generating Transposon Insertion Libraries in Gram-Negative Bacteria for High-Throughput Sequencing
08:19

Generating Transposon Insertion Libraries in Gram-Negative Bacteria for High-Throughput Sequencing

Published on: July 7, 2020

10.7K
A Protocol to Characterize the Morphological Changes of Clostridium difficile in Response to Antibiotic Treatment
12:58

A Protocol to Characterize the Morphological Changes of Clostridium difficile in Response to Antibiotic Treatment

Published on: May 25, 2017

9.1K

相关实验视频

Last Updated: Sep 19, 2025

In vitro Investigation of the MexAB Efflux Pump From Pseudomonas aeruginosa
13:40

In vitro Investigation of the MexAB Efflux Pump From Pseudomonas aeruginosa

Published on: February 17, 2014

12.0K
Generating Transposon Insertion Libraries in Gram-Negative Bacteria for High-Throughput Sequencing
08:19

Generating Transposon Insertion Libraries in Gram-Negative Bacteria for High-Throughput Sequencing

Published on: July 7, 2020

10.7K
A Protocol to Characterize the Morphological Changes of Clostridium difficile in Response to Antibiotic Treatment
12:58

A Protocol to Characterize the Morphological Changes of Clostridium difficile in Response to Antibiotic Treatment

Published on: May 25, 2017

9.1K

科学领域:

  • 微生物学 微生物学
  • 细胞生物学 细胞生物学
  • 药物发现 药物发现 药物发现

背景情况:

  • 结核菌菌的外层菌膜被广泛认为是抗生素治疗的主要障碍.
  • 支持这一假设的先前研究依赖于间接证据或大规模人口测量.

研究的目的:

  • 通过一种新的方法,研究菌根菌膜作为抗生素进入障碍物的作用.
  • 要确定菌膜是否对各种分子和抗生素具有差异性透性.

主要方法:

  • 利用Peptidoglycan可访问性点击介导评估meNt (PAC-MAN) 方法,在活菌根菌的糖层中捕获亚酸修饰的小分子.
  • 应用了PAC-MAN来分析菌膜对光体和抗生素衍生物的差异性限制.

主要成果:

  • 膜被证明可以在两种M.中差异性地限制光体和抗生素衍生物的进入. 结核病 和 M. 结核病 纹体. 纹体. 纹体
  • 在不同类型的抗生素之间以及在诺基诺隆家族内观察到歧视.
  • 对子群体的分析显示,真菌膜对某些光体和万科胺素有异质的限制.

结论:

  • 菌根菌膜作为一个动态的,分子和细胞特异性屏障,防止抗生素透.
  • 这一发现对了解抗生素耐药性和开发针对结核病的新治疗策略具有重大意义.