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相关概念视频

ATP Driven Pumps III: V-type Pumps01:30

ATP Driven Pumps III: V-type Pumps

3.6K
V-type pumps are ATP-driven pumps found in the vacuolar membranes of plants, yeast, endosomal and lysosomal membranes of animal cells, plasma membranes of a few specialized eukaryotic cells, and some prokaryotes. They are also known as the V1Vo-ATPase, that couple ATP hydrolysis to transport protons against a concentration gradient.
The peripheral or cytosolic V1 domain with eight subunits is involved in ATP hydrolysis. The integral or transmembrane V0 domain containing at least five subunits...
3.6K
Primary Active Transport01:29

Primary Active Transport

10.0K
In contrast to passive transport, active transport involves a substance being moved through membranes in a direction against its concentration or electrochemical gradient. There are two types of active transport: primary active transport and secondary active transport. Primary active transport utilizes chemical energy from ATP to drive protein pumps embedded in the cell membrane. With energy from ATP, the pumps transport ions against their electrochemical gradients—a direction they would...
10.0K
ATP Driven Pumps II: P-type Pumps01:34

ATP Driven Pumps II: P-type Pumps

4.6K
The P-type pumps are a large family of integral membrane transporter ATPases. They are divided into five major types based on substrate specificity, from I to V.
A typical P-type pump has three cytosolic domains: nucleotide-binding (N), phosphorylation (P), and activator (A) domains. These domains are connected to the membrane-spanning helices by short amino acid segments. ATP hydrolysis and covalent phosphoenzyme intermediate formation are crucial parts of the catalytic cycle. At the highly...
4.6K
ATP Driven Pumps I: An Overview01:27

ATP Driven Pumps I: An Overview

8.0K
ATP-driven pumps, also known as transport ATPases, are integral membrane proteins. They have binding sites for ATP located on the membrane's cytosolic side and the ion-conducting domain in the transmembrane region. These pumps use the free energy released from ATP hydrolysis to move the solutes across cell membranes against an electrochemical gradient.
There are four main types of ATP-driven pumps - P-type, V-type, F-type, and ABC transporter. All these pumps are of varying complexities and...
8.0K
Pore Transport and Ion-Pair Transport01:17

Pore Transport and Ion-Pair Transport

406
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...
406
Active Transport01:14

Active Transport

567
Active transport is a critical biological process that allows cells to move solutes against an electrochemical gradient. This process requires direct energy input and is characterized by its selectivity, saturability, and susceptibility to competitive inhibition.
Primary active transporters, like Na+, K+ and -ATPase, directly utilize ATP to move ions across the membrane. These transporters play significant roles in various physiological processes. For instance, Na+, K+ and -ATPase maintain...
567

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相关实验视频

Updated: Jun 18, 2025

Functional Characterization of Na+/H+ Exchangers of Intracellular Compartments Using Proton-killing Selection to Express Them at the Plasma Membrane
07:38

Functional Characterization of Na+/H+ Exchangers of Intracellular Compartments Using Proton-killing Selection to Express Them at the Plasma Membrane

Published on: March 30, 2015

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一个分子离子

Baihao Shao1, Heyifei Fu1, Ivan Aprahamian1

  • 1Department of Chemistry, Dartmouth College, Hanover, NH 03755, USA.

Science (New York, N.Y.)
|August 1, 2024
PubMed
概括
此摘要是机器生成的。

研究人员开发了一种新型的人造受体, 这种分子可以精确控制离子捕获和释放,用于人工生物系统的潜在应用.

更多相关视频

Membrane Transport Processes Analyzed by a Highly Parallel Nanopore Chip System at Single Protein Resolution
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Membrane Transport Processes Analyzed by a Highly Parallel Nanopore Chip System at Single Protein Resolution

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A Proteoliposome-Based Efflux Assay to Determine Single-molecule Properties of Cl- Channels and Transporters
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A Proteoliposome-Based Efflux Assay to Determine Single-molecule Properties of Cl- Channels and Transporters

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相关实验视频

Last Updated: Jun 18, 2025

Functional Characterization of Na+/H+ Exchangers of Intracellular Compartments Using Proton-killing Selection to Express Them at the Plasma Membrane
07:38

Functional Characterization of Na+/H+ Exchangers of Intracellular Compartments Using Proton-killing Selection to Express Them at the Plasma Membrane

Published on: March 30, 2015

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Membrane Transport Processes Analyzed by a Highly Parallel Nanopore Chip System at Single Protein Resolution
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Membrane Transport Processes Analyzed by a Highly Parallel Nanopore Chip System at Single Protein Resolution

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A Proteoliposome-Based Efflux Assay to Determine Single-molecule Properties of Cl- Channels and Transporters
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A Proteoliposome-Based Efflux Assay to Determine Single-molecule Properties of Cl- Channels and Transporters

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科学领域:

  • 超分子化学
  • 人工光合作用
  • 离子运输

背景情况:

  • 基于蛋白质的输送物对生物过程至关重要,它们可以在度梯度上移动离子.
  • 由于需要控制的结合和释放,开发模仿这种功能的人工受体具有挑战性.
  • 现有的人工系统往往难以平衡高亲和度与按需的离子传输.

研究的目的:

  • 设计和合成一种能够进行活性离子传输的新型人工受体.
  • 使用光能驱动离子对度梯度的运输.
  • 使用可光切换系统实现对离子捕获和释放的精确和按需控制.

主要方法:

  • 一个基于光开关的三元受体的合成.
  • 使用二甲液体膜进行离子运输实验.
  • 使用光能来启动分子机制.

主要成果:

  • 开发的受体成功地作为一个分子运输离子.
  • 该系统表现出简单的合成,可视化和优秀的光交换特性.
  • 证明了离子的优异开关结合特性,结合差异高达六个数量级.

结论:

  • 已经成功创建了一种能够运输活性离子的新型光开关分子.
  • 接收器有效地将光能转化为离子转移的机械工作.
  • 这种系统为人工离子运输提供了一个有前途的平台,