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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

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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...
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ATP Driven Pumps I: An Overview01:27

ATP Driven Pumps I: An Overview

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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...
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ATP Synthase: Mechanism01:48

ATP Synthase: Mechanism

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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...
16.6K
The Inner Mitochondrial Membrane01:28

The Inner Mitochondrial Membrane

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The inner mitochondrial membrane is the primary site of ATP synthesis. The inner membrane domain that forms a smooth layer adjacent to the outer membrane is called the inner boundary membrane. This domain contains membrane transporters that drive metabolites in and out of the mitochondria.  In contrast, the inner membrane network that invaginates into the matrix space is called the cristae membrane. This domain accounts for principle mitochondrial function as it accommodates the protein...
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Energy to Drive Translocation01:37

Energy to Drive Translocation

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Mitochondrial protein import is powered by two distinct energy sources: ATP hydrolysis and electrochemical potential across the inner membrane. Newly synthesized precursors are bound by cytosolic chaperones of the Hsp70 family, which guide them to the import receptors on the mitochondrial surface. Utilizing the energy of ATP hydrolysis, Hsp70 chaperones transfer these precursors to the TOM receptors on the mitochondrial outer membrane.
Generally, polypeptides are unfolded by two distinct...
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pH Regulation in Cells01:28

pH Regulation in Cells

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pH plays a critical role in maintaining normal cellular activities. It helps maintain the structure and function of various proteins, dictates the charge on cellular membranes, and is crucial for metabolic reactions inside the cell. Moreover, cells use the energy from the proton motive force to generate ATP.
Cytosolic pH
Under physiological conditions, the cytosolic pH is slightly more acidic than the extracellular pH. However, cells must prevent further acidification of their cytosol to...
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相关实验视频

Updated: Jan 9, 2026

Inner Mitochondrial Membrane Sensitivity to Na+ Reveals Partially Segmented Functional CoQ Pools
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空腔型H+-ATPase介导的器官外缓冲解决了线粒体功能障碍.

Geoffray Monteuuis1, Ryan Awadhpersad1, Daan van der Kolk1

  • 1Department of Biochemistry and Developmental Biology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.

Nature communications
|December 3, 2025
PubMed
概括

失去真空类型的H+-ATPase (v-ATPase) 令人惊的是,尽管存在线粒体缺陷,但仍然支持细胞存活. 这一发现揭示了一种新的保护机制,涉及pH调节和细胞平衡的代谢适应.

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Microfluidics-Assisted Selective Depolarization of Axonal Mitochondria
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Mitochondrial Ca2+ Retention Capacity Assay and Ca2+-triggered Mitochondrial Swelling Assay
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相关实验视频

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科学领域:

  • 细胞生物学 细胞生物学
  • 生物化学 生化学
  • 遗传学 遗传学 是一个

背景情况:

  • 线粒体功能障碍与许多人类疾病有关,包括神经退行,癌症和衰老.
  • 细胞平衡依赖于协调的核和线粒体基因表达.
  • 适应机制对于在细胞压力下生存至关重要.

研究的目的:

  • 为了确定细胞途径,在受损的线粒体蛋白质合成期间促进生存.
  • 研究真空类型H+-ATPase (v-ATPase) 在缓解线粒体功能障碍中的作用.

主要方法:

  • 用全基因组的CRISPR淘汰查来识别细胞适应性通路.
  • 实验利用了癌症细胞系和患者衍生的线粒体疾病模型.

主要成果:

  • 已确定v-ATPase的损失是线粒体转化缺陷的强有力的抑制剂.
  • 部分v-ATPase损失调节的线粒体膜潜力 (ΔΨm) 和晶状体结构.
  • 这种调制发生在癌细胞和患者衍生的线粒体疾病模型中.

结论:

  • v-ATPase 作为一种对抗线粒体功能障碍的器官外缓冲机制.
  • 改变pH稳态和代谢重新连接是通过v-ATPase抑制促进的保护性反应.
  • 这些适应性策略在线粒体压力条件下增强细胞适应性.