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

Electron Transport Chain: Complex I and II01:46

Electron Transport Chain: Complex I and II

The mitochondrial electron transport chain (ETC) is the main energy generation system in the eukaryotic cells. However, mitochondria also produce cytotoxic reactive oxygen species (ROS) due to the large electron flow during oxidative phosphorylation. While Complex I is one of the primary sources of superoxide radicals, ROS production by Complex II is uncommon and may only be observed in cancer cells with mutated complexes.
ROS generation is regulated and maintained at moderate levels necessary...
Electron Transport Chain: Complex III and IV01:43

Electron Transport Chain: Complex III and IV

During the electron transport chain, electrons from NADH and FADH2 are first transferred to complexes I and II, respectively. These two complexes then transfer the electrons to ubiquinol, which carries them further to complex III. Complex III passes the electrons across the intermembrane space to Cyt c, which carries them further to complex IV. Complex IV donates electrons to oxygen and reduces it to water. As electrons pass through complexes I, III, and IV, the energy released aids the pumping...
The Nucleosome Core Particle01:12

The Nucleosome Core Particle

Nucleosomes are the DNA-histone complex, where the DNA strand is wound around the histone core. The histone core is an octamer containing two copies of H2A, H2B, H3, and H4 histone proteins.
Nucleosomes, paradoxically, perform two opposite functions simultaneously. On the one hand, their primary aim is to protect the delicate DNA strands from physical damage and help achieve a higher compaction ratio. On the other hand, they must allow polymerase enzymes to access histone-bound DNA during...
The Nucleosome Core Particle02:10

The Nucleosome Core Particle

Nucleosomes are the DNA-histone complex, where the DNA strand is wound around the histone core. The histone core is an octamer containing two copies of H2A, H2B, H3, and H4 histone proteins.
The paradox
Nucleosomes, paradoxically, perform two opposite functions simultaneously. On the one hand, their main responsibility is to protect the delicate DNA strands from physical damage and help achieve a higher compaction ratio. While on the other hand, they must allow polymerase enzymes to access DNA...
Valence Bond Theory02:42

Valence Bond Theory

Coordination compounds and complexes exhibit different colors, geometries, and magnetic behavior, depending on the metal atom/ion and ligands from which they are composed. In an attempt to explain the bonding and structure of coordination complexes, Linus Pauling proposed the valence bond theory, or VBT, using the concepts of hybridization and the overlapping of the atomic orbitals. According to VBT, the central metal atom or ion (Lewis acid) hybridizes to provide empty orbitals of suitable...
Metal-Ligand Bonds02:51

Metal-Ligand Bonds

The hemoglobin in the blood, the chlorophyll in green plants, vitamin B-12, and the catalyst used in the manufacture of polyethylene all contain coordination compounds. Ions of the metals, especially the transition metals, are likely to form complexes.
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...

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

Redox-protonation landscape of indene-annulated perylenes: chemodivergent switching of multistate NIR chromophores.

Chemical science·2026
Same author

Clarifying the Unknown Mechanism of the Removal of the 4-Nitrobenzyloxymethyl Group via a Benzyl Radical Intermediate Induced by Tetra-<i>n</i>-butylammonium Fluoride.

Organic letters·2026
Same author

Unveiling the emission mechanism in analog-doped carbazole-based organic afterglow materials.

Nature communications·2026
Same author

One-pot asymmetric sulfoxidation using <i>in situ</i> generated H<sub>2</sub>O<sub>2</sub> from H<sub>2</sub> and O<sub>2</sub> catalyzed by rhodium and vanadium complexes.

Chemical communications (Cambridge, England)·2026
Same author

Circularly Polarized Long-Persistent and Photostimulated Luminescence Enabled through Förster Resonance Energy Transfer and Upconversion Strategies.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026
Same author

Investigating charge accumulation mechanisms in organic materials via slow transient emission spectroscopy.

Science advances·2025

相关实验视频

Updated: Jul 15, 2026

Imine Metathesis by Silica-Supported Catalysts Using the Methodology of Surface Organometallic Chemistry
09:37

Imine Metathesis by Silica-Supported Catalysts Using the Methodology of Surface Organometallic Chemistry

Published on: October 18, 2019

一个由H2衍生的双核Ni(mu-H) Ru复合体.

Seiji Ogo1, Ryota Kabe, Keiji Uehara

  • 1Center for Future Chemistry, Kyushu University, Fukuoka 819-0395, Japan. ogo-tcm@mbox.nc.kyushu-u.ac.jp

Science (New York, N.Y.)
|April 28, 2007
PubMed
概括

研究人员合成了一种偏磁的-复合体,模仿[NiFe]酶酶的活性位点. 这种双核复合体,具有桥接化连接体,为酶的活性形式提供结构模拟物.

更多相关视频

The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes
10:51

The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes

Published on: April 10, 2015

Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase
10:01

Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase

Published on: December 4, 2017

相关实验视频

Last Updated: Jul 15, 2026

Imine Metathesis by Silica-Supported Catalysts Using the Methodology of Surface Organometallic Chemistry
09:37

Imine Metathesis by Silica-Supported Catalysts Using the Methodology of Surface Organometallic Chemistry

Published on: October 18, 2019

The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes
10:51

The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes

Published on: April 10, 2015

Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase
10:01

Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase

Published on: December 4, 2017

科学领域:

  • 生物有机化学 生物有机化学
  • 有机金属化学 有机金属化学
  • 酶活性部位建模 酶活性部位建模

背景情况:

  • [NiFe]酶酶对于生物代谢至关重要.
  • 在研究中复制酶的活性部位结构是很困难的.
  • 了解活性部位是开发人工催化剂的关键.

研究的目的:

  • 合成和描述[NiFe]酶活性位点的稳定模型复合物.
  • 为了研究二核-复合体对H2的异质裂变.
  • 为拟议的酶活性形式提供结构模拟物.

主要方法:

  • 一个双核NiRu水化合物的合成.
  • 在水中的环境条件下与H2发生反应.
  • 通过中子衍射分离和结构性确定对磁性Ni (mu-H) Ru复合体.

主要成果:

  • 成功分离了一种具有磁性双核-复合体与桥接化连接体.
  • 该复合体是通过H2.2的异质裂解形成的.
  • 中子衍射证实了六坐标的Ni (mu-H) Ru结构.

结论:

  • 合成的Ni(mu-H) Ru复合体作为[NiFe]酶的活性形式的密切结构模拟物.
  • 这个模型提供了对酶的催化机制的洞察.
  • 这项研究表明,在温和条件下制备活性部位模拟剂的可行方法.