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

Receptor Tyrosine Kinases01:26

Receptor Tyrosine Kinases

18.0K
Receptor tyrosine kinases or RTKs are membrane-bound receptors that phosphorylate specific tyrosine on protein substrates. RTKs regulate cellular growth, differentiation, survival, and migration. They contain an extracellular ligand binding domain, a transmembrane domain, and a cytosolic tail with intrinsic kinase activity. Several extracellular signaling molecules activate RTKs in one or more ways and relay the signal downstream. Ligands such as platelet-derived growth factor (PDGF) or...
18.0K
Enzyme-linked Receptors01:00

Enzyme-linked Receptors

86.0K
Enzyme-linked receptors are proteins that act as both receptor and enzyme, activating multiple intracellular signals. This is a large group of receptors that include the receptor tyrosine kinase (RTK) family. Many growth factors and hormones bind to and activate the RTKs.
Neurotrophin (NT) receptors are a family of RTKs, including trkA, trkB, and trkC (tropomyosin-related kinase) receptors. TrkA is specific for nerve growth factor (NGF), neurotrophin-6, and neurotrophin-7. TrkB binds...
86.0K
Transducer Mechanism: Enzyme-Linked Receptors01:27

Transducer Mechanism: Enzyme-Linked Receptors

3.9K
Enzyme-linked receptors are cell-surface receptors acting as an enzyme or associating with an enzyme intracellularly. They make excellent drug targets. Drugs can bind to the extracellular ligand-binding domain or directly affect their enzymatic domain and alter their activity.
Major types that are helpful drug targets include:
3.9K
Amplifying Signals via Enzymatic Cascade01:22

Amplifying Signals via Enzymatic Cascade

17.5K
When a ligand binds to a cell-surface receptor, the receptor's intracellular domain changes shape, which may either activate its enzyme function or allow its binding to other molecules. The initial signal is amplified by most signal transduction pathways. This means that a single ligand molecule can activate multiple molecules of a downstream target. Proteins that relay a signal are most commonly phosphorylated at one or more sites, activating or inactivating the protein. Kinases catalyze...
17.5K
Assembly of Signaling Complexes01:30

Assembly of Signaling Complexes

6.5K
Multiprotein signaling complexes are formed in a dynamic process involving protein-protein interactions at the cytoplasmic domain of transmembrane receptors or enzymatic and non-enzymatic proteins associated with the receptor. These complexes ensure the activation and propagation of intracellular signals that regulate cell functions.
Interaction domains in cell signaling
Interaction domains recognize exposed features of their binding partners containing post-translationally modified sequences,...
6.5K

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 tunable CTD grammar governs the spatial programming of the transcription cycle.

Nature communications·2026
Same author

CLaSSiNet: A Computational Framework for High-Resolution Classification and Spatial Mapping of Heterogeneous Biological Network Architectures.

JACS Au·2026
Same author

FLEXTAG: a small and self-renewable protein labeling system for anti-fading multi-color super-resolution imaging.

Nature communications·2026
Same author

Actin depolymerization promotes axon regeneration by restoring axonal mitochondrial transport in mouse models of optic neuropathy.

Science translational medicine·2026
Same author

Membrane-associated periodic skeleton regulates major forms of endocytosis in neurons through a signaling-driven positive feedback loop.

Science advances·2026
Same author

Tunable Chemical and Optical Control of ER-Plasma Membrane Contact Site Geometry and Dynamics with High-Fidelity Visualization.

bioRxiv : the preprint server for biology·2026

相关实验视频

Updated: Jan 17, 2026

Light-mediated Reversible Modulation of the Mitogen-activated Protein Kinase Pathway during Cell Differentiation and Xenopus Embryonic Development
09:32

Light-mediated Reversible Modulation of the Mitogen-activated Protein Kinase Pathway during Cell Differentiation and Xenopus Embryonic Development

Published on: June 15, 2017

9.2K

一个可化学诱导的多元化系统,用于可调和无背景RTK激活.

Yuanmin Zheng1,2, Jinyu Fei1, Abhirup Chakrabarti3

  • 1Department of Chemistry, The Pennsylvania State University, University Park, PA 16802, USA.

bioRxiv : the preprint server for biology
|September 18, 2025
PubMed
概括

我们开发了一种新的化学系统来控制受体氨酸激酶 (RTK) 和它们的信号通路,如ERK. 该系统精确地激活RTK集群和下游效应,最大限度地减少不必要的背景激活,以改善细胞生物学研究.

更多相关视频

Spatial and Temporal Control of T Cell Activation Using a Photoactivatable Agonist
07:48

Spatial and Temporal Control of T Cell Activation Using a Photoactivatable Agonist

Published on: April 25, 2018

6.6K
An Engineered Split-TET2 Enzyme for Chemical-inducible DNA Hydroxymethylation and Epigenetic Remodeling
08:34

An Engineered Split-TET2 Enzyme for Chemical-inducible DNA Hydroxymethylation and Epigenetic Remodeling

Published on: December 18, 2017

7.0K

相关实验视频

Last Updated: Jan 17, 2026

Light-mediated Reversible Modulation of the Mitogen-activated Protein Kinase Pathway during Cell Differentiation and Xenopus Embryonic Development
09:32

Light-mediated Reversible Modulation of the Mitogen-activated Protein Kinase Pathway during Cell Differentiation and Xenopus Embryonic Development

Published on: June 15, 2017

9.2K
Spatial and Temporal Control of T Cell Activation Using a Photoactivatable Agonist
07:48

Spatial and Temporal Control of T Cell Activation Using a Photoactivatable Agonist

Published on: April 25, 2018

6.6K
An Engineered Split-TET2 Enzyme for Chemical-inducible DNA Hydroxymethylation and Epigenetic Remodeling
08:34

An Engineered Split-TET2 Enzyme for Chemical-inducible DNA Hydroxymethylation and Epigenetic Remodeling

Published on: December 18, 2017

7.0K

科学领域:

  • 细胞生物学 细胞生物学
  • 分子信号传输的方法
  • 生物技术是生物技术.

背景情况:

  • 受体氨酸激酶 (RTK) 通过将外部信号传递到细胞中来控制细胞的基本功能.
  • 现有的光感应RTK系统存在高基底激活,导致过早信号发送.
  • 对RTK激活的精确控制对于研究细胞动态和工程细胞行为至关重要.

研究的目的:

  • 开发一种具有最小基底激活的化学诱导RTK系统.
  • 为了实现RTK集群和下游信号事件的可视化.
  • 精确剖析RTK介导的信号动态,设计细胞行为.

主要方法:

  • 开发一种新的化学诱导RTK系统.
  • 单细胞成像可视化RTK聚类和膜骨架动态.
  • RTK集群丰度与ERK酸化水平的相关性.

主要成果:

  • 与以前的系统相比,化学系统显著降低了基底RTK激活.
  • 可见的RTK集群在诱导后形成,与ERK酸化直接相关.
  • 基于光谱的膜骨架的ERK-依赖性分解仅在诱导后发生.

结论:

  • 新的化学诱导RTK系统为RTK信号提供了精确的时空控制.
  • 这个平台可以准确地剖析RTK介导的信号通路.
  • 该系统是基础细胞生物学研究和工程应用的宝贵工具.