线粒体ATP合成酶的访问质子路径的祖先形状由一个分裂子单元-a揭示
Jonathan E Wong1,2, Alena Zíková1,2, Ondřej Gahura1
1Institute of Parasitology, Biology Centre, Czech Academy of Sciences, České Budějovice, Czech Republic.
Molecular biology and evolution
|June 20, 2023
概括
F1Fo-ATP合成酶子单元-a的N端α螺旋决定了质子进入线粒体ATP合成的过程. 这种关键的结构元素在真核生物和阿尔法蛋白质细菌中保存,早于真核生物,起源于线粒体祖先.
科学领域:
- 生物化学 生化学
- 分子生物学分子生物学
- 进化生物学 进化生物学
背景情况:
- F1Fo-ATP合成酶通过利用跨膜的质子流产生ATP.
- 质子转位途径的精确机制和进化历史仍然不完全理解.
研究的目的:
- 阐明特定结构元素在确定线粒体ATP合成酶内的质子进入点中的作用.
- 为了研究这些质子通路的进化起源.
主要方法:
- 在各种生物体中对F1Fo-ATP合成酶结构进行比较分析.
- 识别保护的蛋白质域及其功能影响.
主要成果:
- 一个小单元-a的短N端α螺旋定义了线粒体ATP合成酶的光半通道中的质子进入点和通路.
- 这种α螺旋在真核生物和α蛋白细菌中保存,但在其他细菌中不存在.
- α螺旋阻断了细菌ATP合成酶中存在的两个质子进入路径之一,在线粒体谱系中建立了一个单一的进入点.
结论:
- 亚单元-a的N端α螺旋是真核和α-proteobacterial ATP合成酶中质子转位的关键决定因素.
- 定义质子接入通道的结构特征起源于真核生物出现之前,在导致线粒体的进化谱系中.
相关概念视频
ATP Synthase: Mechanism
14.8K
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...
14.8K
ATP Synthase: Structure
12.7K
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...
12.7K
Chemiosmosis and ATP Synthesis
60
The electron transport chain is a critical component of cellular respiration, occurring in the inner mitochondrial membrane. It facilitates the transfer of high-energy electrons from reduced cofactors NADH and FADH₂ to molecular oxygen, the final electron acceptor. This transfer of electrons through a series of protein complexes is tightly coupled to the translocation of protons across the membrane, generating a proton gradient essential for ATP synthesis.Electron Flow and Proton...
60
Energy to Drive Translocation
2.1K
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...
Generally, polypeptides are unfolded by two distinct...
2.1K
The ADP/ATP Carrier Protein
3.3K
ADP/ATP carrier or AAC protein is the most abundant carrier protein in the inner mitochondrial membrane. It transports large quantities of ADP and ATP, equivalent to the average human body weight, every day. Among other transporters, ACC protein is one of the best-studied members of the mitochondrial carrier protein family. The ADP/ATP carrier protein comprises two transmembrane helices connected to a loop and a single alpha-helix on the matrix side. It switches between two conformational...
3.3K
The Inner Mitochondrial Membrane
3.5K
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...
3.5K


