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

The Replisome03:01

The Replisome

32.8K
DNA replication is carried out by a large complex of proteins that act in a coordinated matter to achieve high-fidelity DNA replication. Together this complex is known as the DNA replication machinery or the replisome.
The synthesis of the leading and lagging strands is a highly coordinated process. To explain this, the “Trombone model” was proposed by Bruce Alberts in 1980. The DNA loop formation starts when a primer is synthesized on the parent lagging strand. The loop grows with...
32.8K
ATP Synthase: Mechanism01:48

ATP Synthase: Mechanism

13.8K
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...
13.8K
Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

5.7K
DNA replication is initiated at sites containing predefined DNA sequences known as origins of replication. DNA is unwound at these sites by the minichromosome maintenance (MCM) helicase and other factors such as Cdc45 and the associated GINS complex.The unwound single strands are protected by replication protein A (RPA) until DNA polymerase starts synthesizing DNA at the 5’ end of the strand in the same direction as the replication fork. To prevent the replication fork from falling apart,...
5.7K
ATP Synthase: Structure01:18

ATP Synthase: Structure

11.8K
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...
11.8K
Membrane Asymmetry Regulating Transporters01:19

Membrane Asymmetry Regulating Transporters

4.3K
Enzymes like flippase, floppase, and scramblase transfer phospholipids from one layer to another in the membrane, thereby affecting membrane asymmetry.
Flippase
Eukaryotic flippases are type-IV P-type ATPases or P4-ATPases belonging to P-type ATPase family proteins that are membrane-bound pumps involved in the ATP-mediated transport of ions and molecules across the membrane. Flippases flip specific phospholipids from the outer to the inner leaflet of a membrane. All P4-ATPases have one...
4.3K
Translesion DNA Polymerases02:10

Translesion DNA Polymerases

9.7K
Translesion (TLS) polymerases rescue stalled DNA polymerases at sites of damaged bases by replacing the replicative polymerase and installing a nucleotide across the damaged site. Doing so, TLS allows additional time for the cell to repair the damage before resuming regular DNA replication.
TLS polymerases are found in all three domains of life - archaea, bacteria, and eukaryotes. Of the different classes of TLS polymerases, members of the Y family are fitted with specialized structures that...
9.7K

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

Engineered T7 RNA polymerase to improve mRNA capping efficiency and reduce dsRNA generation during <i>in vitro</i> transcription.

Molecular therapy. Advances·2026
Same author

Engineered chimeric T7 RNA polymerase improves salt tolerance and reduces dsRNA impurity generation during in vitro transcription of mRNA.

Nucleic acids research·2025
Same author

REV1 inhibition enhances trinucleotide repeat mutagenesis.

bioRxiv : the preprint server for biology·2025
Same author

Divide-and-conquer strategy for NMR studies of the E. coli γ-clamp loader complex.

Journal of biomolecular NMR·2025
Same author

Distal residues contribute to enzymatic catalysis in human phosphoglucose isomerase through modulation of dynamics and electrostatics.

The Journal of chemical physics·2025
Same author

Long-Range Destabilizing Effects of Mutations at the <i><i>Escherichia coli</i></i> β Clamp Dimer Interface.

Biochemistry·2025

相关实验视频

Updated: May 23, 2025

Dissecting Mechanoenzymatic Properties of Processive Myosins with Ultrafast Force-Clamp Spectroscopy
09:38

Dissecting Mechanoenzymatic Properties of Processive Myosins with Ultrafast Force-Clamp Spectroscopy

Published on: July 1, 2021

1.3K

过程性膜蛋白的功能不对称性

Sam Mahdi1, Penny J Beuning2, Dmitry M Korzhnev1

  • 1Department of Molecular Biology and Biophysics, University of Connecticut Health Center, Farmington, Connecticut.

Biophysical journal
|April 18, 2025
PubMed
概括

对称的蛋白质复合体,如过程性,在生物功能过程中经常失去对称性. 本综述探讨了对称性和不对称性在调节DNA复制和修复中的活动中的关键作用.

科学领域:

  • 生物化学 生物化学
  • 分子生物学分子生物学
  • 结构生物学 结构生物学

背景情况:

  • 对称的同类寡合蛋白质在生命中很常见.
  • 渐进性是参与DNA复制和修复的关键对称蛋白质复合体.
  • 这些复合体往往从对称转变为不对称,以执行功能.

研究的目的:

  • 为了审查过程性的对称性和不对称性.
  • 讨论这些状态在生物过程中的功能影响.
  • 要突出支持功能不对称的证据.

主要方法:

  • 结构,生物物理和计算研究的文献综述.
  • 分析蛋白质复合体的形状变化.
  • 检查影响蛋白质功能的翻译后修改.

主要成果:

  • 顺序性,虽然最初是对称的,但在功能过程中经历了不对称的变化.
  • 不对称的中间体参与了紧固件负荷和相互作用.
  • 翻译后的修改,如无处不在和SUMOylation,有助于功能不对称.

结论:

更多相关视频

ACT1-CUP1 Assays Determine the Substrate-Specific Sensitivities of Spliceosomal Mutants in Budding Yeast
07:31

ACT1-CUP1 Assays Determine the Substrate-Specific Sensitivities of Spliceosomal Mutants in Budding Yeast

Published on: June 30, 2022

2.4K
Comparing the Affinity of GTPase-binding Proteins using Competition Assays
10:37

Comparing the Affinity of GTPase-binding Proteins using Competition Assays

Published on: October 8, 2015

9.1K

相关实验视频

Last Updated: May 23, 2025

Dissecting Mechanoenzymatic Properties of Processive Myosins with Ultrafast Force-Clamp Spectroscopy
09:38

Dissecting Mechanoenzymatic Properties of Processive Myosins with Ultrafast Force-Clamp Spectroscopy

Published on: July 1, 2021

1.3K
ACT1-CUP1 Assays Determine the Substrate-Specific Sensitivities of Spliceosomal Mutants in Budding Yeast
07:31

ACT1-CUP1 Assays Determine the Substrate-Specific Sensitivities of Spliceosomal Mutants in Budding Yeast

Published on: June 30, 2022

2.4K
Comparing the Affinity of GTPase-binding Proteins using Competition Assays
10:37

Comparing the Affinity of GTPase-binding Proteins using Competition Assays

Published on: October 8, 2015

9.1K
  • 对称与不对称之间的过渡对于流动性管调节至关重要.
  • 功能不对称性使得DNA复制和修复之间的各种相互作用和过渡成为可能.
  • 了解的不对称性为DNA代谢调节提供了洞察力.