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相关概念视频

ATP Synthase: Structure01:18

ATP Synthase: Structure

13.2K
ATP synthase or ATPase is among the most conserved proteins found in bacteria, mammals, and plants. This enzyme can catalyze a forward reaction in response to the electrochemical gradient, producing ATP from ADP and inorganic phosphate. ATP synthase can also work in a reverse direction by hydrolyzing ATP and generating an electrochemical gradient. Different forms of ATP synthases have evolved special features to meet the specific demands of the cell. Based on their specific feature, ATP...
13.2K
ATP Synthase: Mechanism01:48

ATP Synthase: Mechanism

15.3K
In animals, the mitochondrial F1F0 ATP synthase is the key protein that synthesizes ATP molecules through a complex catalytic mechanism. While the nuclear genome encodes the majority of ATP synthase subunits, the mitochondrial genome encodes some of the enzyme's most critical components. The formation of this multi-subunit enzyme is a complex multi-step process regulated at the level of transcription, translation, and assembly. Defects in one or more of these steps can result in decreased...
15.3K
ATP Driven Pumps I: An Overview01:27

ATP Driven Pumps I: An Overview

8.6K
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...
8.6K
ATP Driven Pumps II: P-type Pumps01:34

ATP Driven Pumps II: P-type Pumps

5.2K
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...
5.2K
ATP Driven Pumps III: V-type Pumps01:30

ATP Driven Pumps III: V-type Pumps

4.0K
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...
4.0K
Protein Dynamics in Living Cells01:19

Protein Dynamics in Living Cells

2.3K
Different fluorescence-based techniques are used to study the protein dynamics in living cells. These techniques include FRAP, FRET, and PET.
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
2.3K

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相关实验视频

Updated: Sep 20, 2025

Visualization of ATP Synthase Dimers in Mitochondria by Electron Cryo-tomography
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Visualization of ATP Synthase Dimers in Mitochondria by Electron Cryo-tomography

Published on: September 14, 2014

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使用Janus纳米粒子可视化单个V-ATPase旋转.

Akihiro Otomo1,2, Jared Wiemann3, Swagata Bhattacharyya3

  • 1Institute for Molecular Science, National Institutes of National Sciences, Okazaki, Aichi 444-8787, Japan.

Nano letters
|November 22, 2024
PubMed
概括
此摘要是机器生成的。

这项研究引入了Janus纳米粒子,用于直接可视化单个V-ATPase电机旋转. 这种新的方法准确地测量扭矩,推进了旋转电机的单分子分析.

关键词:
亚努斯纳米颗粒的使用波动定理 波动定理旋转的ATPases可以使用.旋转跟踪的跟踪方式一个分子分析分析.扭矩测量的扭矩测量

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Single-Molecule FRET Imaging for Observing the Conformational Dynamics of Dynamin-Like GTPase Atlastin
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Single-Molecule FRET Imaging for Observing the Conformational Dynamics of Dynamin-Like GTPase Atlastin

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Visualizing Actin and Microtubule Coupling Dynamics In Vitro by Total Internal Reflection Fluorescence TIRF Microscopy
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Visualizing Actin and Microtubule Coupling Dynamics In Vitro by Total Internal Reflection Fluorescence TIRF Microscopy

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相关实验视频

Last Updated: Sep 20, 2025

Visualization of ATP Synthase Dimers in Mitochondria by Electron Cryo-tomography
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Visualization of ATP Synthase Dimers in Mitochondria by Electron Cryo-tomography

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Single-Molecule FRET Imaging for Observing the Conformational Dynamics of Dynamin-Like GTPase Atlastin
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Visualizing Actin and Microtubule Coupling Dynamics In Vitro by Total Internal Reflection Fluorescence TIRF Microscopy
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科学领域:

  • 生物物理学的生物物理.
  • 纳米技术纳米技术
  • 生物化学 生物化学

背景情况:

  • 旋转分子电机,如V-ATPases,对于细胞功能至关重要.
  • 想象单个分子的旋转是理解它们机制的关键.
  • 传统的纳米粒子 (NP) 追踪方法间接推断出旋转.

研究的目的:

  • 开发一种使用Janus NPs.进行单个V-ATPase旋转的直接成像方法.
  • 为了评估Janus NPs在旋转电机扭矩测量的准确性.
  • 突出了Janus NP在传统探测器上的优势.

主要方法:

  • 采用了用于成像的非对称光学对比度的/金Janus NP.
  • 在表面上固定单个V-ATPase电机来自*Enterococcus hirae*.
  • 分析了单向反时针旋转,并测量了扭矩.

主要成果:

  • 成功成像了单个V-ATPase电机的直接旋转.
  • 证明了精确的扭矩测量,尽管Janus NP的粘性负载.
  • 与传统探头相比,展示了Janus NPs的优越性能.

结论:

  • 詹努斯NP提供了一个强大的工具,用于直接单分子可视化旋转电机.
  • 这种方法提高了我们对V-ATPase功能和扭矩生成的理解.
  • 该方法对于研究其他旋转分子机器具有广泛的适用性.