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

Interactions Between Signaling Pathways01:19

Interactions Between Signaling Pathways

6.3K
Signaling cascades usually lack linearity. Multiple pathways interact and regulate one another, allowing cells to integrate and respond to diverse environmental stimuli.
Convergence and divergence, and cross-talk between signaling pathways
Two distinct signaling pathways can converge on a single functional unit, which may either be a single protein or a complex of proteins. The response is either functionally distinct or synergistic between the two pathways but different from the response...
6.3K
Covalently Linked Protein Regulators02:04

Covalently Linked Protein Regulators

6.9K
Proteins can undergo many types of post-translational modifications, often in response to changes in their environment. These modifications play an important role in the function and stability of these proteins. Covalently linked molecules include functional groups, such as methyl, acetyl, and phosphate groups, and also small proteins, such as ubiquitin. There are around 200 different types of covalent regulators that have been identified.
These groups modify specific amino acids in a protein....
6.9K
Protein Kinases and Phosphatases02:54

Protein Kinases and Phosphatases

13.2K
Proteins undergo chemical modifications that trigger changes in the charge, structure, and conformation of the proteins. Phosphorylation, acetylation, glycosylation, nitrosylation, ubiquitination, lipidation, methylation, and proteolysis are various protein modifications that regulate protein activity. Such modifications are usually enzyme-driven.
Protein kinases
Many proteins in the cell are regulated by phosphorylation, the addition of a phosphate group. A family of enzymes called kinases...
13.2K
PI3K/mTOR/AKT Signaling Pathway01:22

PI3K/mTOR/AKT Signaling Pathway

3.7K
The mammalian target of rapamycin  (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1  (mTORC1) and mTOR complex 2  (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast,  mTORC2 consists of a...
3.7K
Cohesins02:20

Cohesins

4.6K
Cohesin protein complexes are a molecular glue that holds two sister chromatids together. They play an important role both in mitosis and meiosis. In mitosis, all cohesin complexes present on the chromosomes are removed before the start of the anaphase stage.
Cohesin complexes in Meiotic Division
Meiosis involves two distinct rounds of chromosomal segregation and cell divisions— Meiosis I followed by Meiosis II – producing four daughter cells. Meiosis I includes the separation of...
4.6K
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

3.8K
The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
3.8K

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

A neutrophil-intrinsic CKLF1-PKM2 axis drives glycolytic flux for de novo DAG synthesis and pro-inflammatory ROS production.

Cell death and differentiation·2026
Same author

PKM2-mediated metabolic reprogramming of microglia in neuroinflammation.

Cell death discovery·2025
Same author

CKLF1 disrupts microglial efferocytosis following acute ischemic stroke by binding to phosphatidylserine.

Cell death and differentiation·2025
Same author

New perspective on central nervous system disorders: focus on mass spectrometry imaging.

Analytical methods : advancing methods and applications·2024
Same author

Perspective and Therapeutic Potential of the Noncoding RNA-Connexin Axis.

International journal of molecular sciences·2024
Same author

New perspective on sustained antidepressant effect: focus on neurexins regulating synaptic plasticity.

Cell death discovery·2024

相关实验视频

Updated: Jul 23, 2025

Nuclear Magnetic Resonance Spectroscopy for the Identification of Multiple Phosphorylations of Intrinsically Disordered Proteins
12:47

Nuclear Magnetic Resonance Spectroscopy for the Identification of Multiple Phosphorylations of Intrinsically Disordered Proteins

Published on: December 27, 2016

18.8K

康尼克素43酸化:对多种疾病的影响

Meng Zhang1, Zhen-Zhen Wang1, Nai-Hong Chen1

  • 1State Key Laboratory of Bioactive Substances and Functions of Natural Medicines, Institute of Materia Medica & Neuroscience Center, Chinese Academy of Medical Science and Peking Union Medical College, Beijing 100050, China.

Molecules (Basel, Switzerland)
|July 14, 2023
PubMed
概括

康涅素43 (Cx43) 酸化影响了隙间结功能和细胞间通信. 了解Cx43酸化是开发心血管和神经疾病治疗策略的关键.

科学领域:

  • 分子生物学分子生物学
  • 细胞生物学 细胞生物学
  • 生理学 生理学 生理学

背景情况:

  • 连素43 (Cx43) 在哺乳动物的心血管和神经系统中丰富.
  • Cx43酸化是由多个激酶和酸酶调节的,影响其功能.
  • 酸化会影响Cx43的合成,组装和间隙结 (GJ) 特性.

研究的目的:

  • 审查Cx43酸化在各种疾病中的功能意义.
  • 讨论Cx43作为Cx43相关病理生理学的潜在药物标.
  • 要突出Cx43在心脏和神经保护中的作用.

主要方法:

  • 临床和临床前发现的文献综述.
  • 对Cx43酸化对GJ功能影响的分析.
  • 探索Cx43作为治疗目标.

主要成果:

  • Cx43酸化调节了GJ的透性,电导率和门.
  • 改变的Cx43酸化会在生理和病理条件下影响细胞间的通信.
  • 化Cx43在各种疾病过程中起作用.

结论:

关键词:
连接器 43 连接器 43细胞间通信是细胞间的通信.酸化的方法是:光化.心血管系统是心血管系统.神经系统中的神经系统.

更多相关视频

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
09:34

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease

Published on: April 4, 2018

33.8K
Identification of Cyclin-dependent Kinase 1 Specific Phosphorylation Sites by an In Vitro Kinase Assay
12:26

Identification of Cyclin-dependent Kinase 1 Specific Phosphorylation Sites by an In Vitro Kinase Assay

Published on: May 3, 2018

18.7K

相关实验视频

Last Updated: Jul 23, 2025

Nuclear Magnetic Resonance Spectroscopy for the Identification of Multiple Phosphorylations of Intrinsically Disordered Proteins
12:47

Nuclear Magnetic Resonance Spectroscopy for the Identification of Multiple Phosphorylations of Intrinsically Disordered Proteins

Published on: December 27, 2016

18.8K
Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
09:34

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease

Published on: April 4, 2018

33.8K
Identification of Cyclin-dependent Kinase 1 Specific Phosphorylation Sites by an In Vitro Kinase Assay
12:26

Identification of Cyclin-dependent Kinase 1 Specific Phosphorylation Sites by an In Vitro Kinase Assay

Published on: May 3, 2018

18.7K
  • 澄清Cx43酸化与疾病的关系可以提高对疾病的理解.
  • Cx43代表了对心血管和神经疾病的有前途的治疗点.
  • 向Cx43酸化为心脏和神经保护策略提供了潜力.