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相关概念视频

G Protein-coupled Receptors01:15

G Protein-coupled Receptors

12.1K
G Protein-Coupled Receptors or GPCRs are membrane-bound receptors that transiently associate with heterotrimeric G proteins and induce an appropriate response to sensory stimuli such as light, odors, hormones, cytokines, or neurotransmitters.
GPCRs are also called heptahelical, 7TM, or serpentine receptors, and consist of seven (H1-H7) transmembrane alpha-helices that span the bilayer to form a cylindrical core. The transmembrane helices are connected by three extracellular loops and three...
12.1K
Transducer Mechanism: G Protein–Coupled Receptors01:30

Transducer Mechanism: G Protein–Coupled Receptors

2.0K
G Protein–Coupled Receptors (GPCRs) are membrane-bound receptors that transiently associate with heterotrimeric G proteins and induce an appropriate response to various stimuli. GPCRs regulate critical physiological pathways and are excellent drug targets for treating diseases such as diabetes, cancer, obesity, depression, or Alzheimer's. Nearly 35% of approved drugs implement their therapeutic effects by selectively interacting with specific GPCRs.
GPCRs are also called heptahelical,...
2.0K
Cryo-electron Microscopy01:28

Cryo-electron Microscopy

3.3K
Conventional electron microscopy (EM) involves dehydration, fixation, and staining of biological samples, which distorts the native state of biological molecules and results in several artifacts. Also, the high-energy electron beam damages the sample and makes it difficult to obtain high-resolution images. These issues can be addressed using cryo-EM, which uses frozen samples and gentler electron beams. The technique was developed by Jacques Dubochet, Joachim Frank, and Richard Henderson, for...
3.3K
Super-resolution Fluorescence Microscopy01:37

Super-resolution Fluorescence Microscopy

7.0K
Super-resolution fluorescence microscopy (SRFM) provides a better resolution than conventional fluorescence microscopy by reducing the point spread function (PSF). PSF is the light intensity distribution from a point that causes it to appear blurred. Due to PSF, each fluorescing point appears bigger than its actual size, and it is the PSF interference of nearby fluorophores that causes the blurred image. Various approaches to achieving higher resolution through SRFM have recently been...
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相关实验视频

Updated: Jul 8, 2025

G Protein-selective GPCR Conformations Measured Using FRET Sensors in a Live Cell Suspension Fluorometer Assay
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G Protein-selective GPCR Conformations Measured Using FRET Sensors in a Live Cell Suspension Fluorometer Assay

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显微镜和光谱方法研究GPCR结构和功能.

Tomáš Fessl1, Maria Majellaro2, Alexey Bondar1,3

  • 1Faculty of Science, University of South Bohemia, České Budějovice, Czech Republic.

British journal of pharmacology
|December 13, 2023
PubMed
概括
此摘要是机器生成的。

先进的光学显微镜和光谱能够详细观察生物系统中的G蛋白合受体 (GPCR) 信号通路. 这些技术提供了高分辨率的研究细胞信号与最小的干扰.

关键词:
这是一种G蛋白质蛋白质,G蛋白质蛋白质.G蛋白结合受体的受体是G蛋白结合受体的受体.生物传感器生物传感器细胞信号传输的信号.显微镜 显微镜是指使用显微镜.频谱学是一种光谱学.超级分辨率的超级分辨率

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In vivo Quantification of G Protein Coupled Receptor Interactions using Spectrally Resolved Two-photon Microscopy
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In vivo Quantification of G Protein Coupled Receptor Interactions using Spectrally Resolved Two-photon Microscopy

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Strategic Screening and Characterization of the Visual GPCR-mini-G Protein Signaling Complex for Successful Crystallization
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Strategic Screening and Characterization of the Visual GPCR-mini-G Protein Signaling Complex for Successful Crystallization

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相关实验视频

Last Updated: Jul 8, 2025

G Protein-selective GPCR Conformations Measured Using FRET Sensors in a Live Cell Suspension Fluorometer Assay
09:12

G Protein-selective GPCR Conformations Measured Using FRET Sensors in a Live Cell Suspension Fluorometer Assay

Published on: September 10, 2016

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In vivo Quantification of G Protein Coupled Receptor Interactions using Spectrally Resolved Two-photon Microscopy
14:26

In vivo Quantification of G Protein Coupled Receptor Interactions using Spectrally Resolved Two-photon Microscopy

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Strategic Screening and Characterization of the Visual GPCR-mini-G Protein Signaling Complex for Successful Crystallization
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Strategic Screening and Characterization of the Visual GPCR-mini-G Protein Signaling Complex for Successful Crystallization

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科学领域:

  • 细胞生物学 细胞生物学
  • 生物物理学的生物物理.
  • 生物化学 生物化学

背景情况:

  • G蛋白结合受体 (GPCRs) 介导信号转导,用于各种刺激,如光,气味,神经递质和激素.
  • 了解GPCR结构和功能动态需要高分辨率,实时观察信号级联.
  • 内生系统和活细胞需要不扰乱的研究方法.

研究的目的:

  • 审查GPCR信号研究的光学显微镜和光谱学的最新进展.
  • 为突出提供高空间和时间分辨率研究细胞信号的技术.
  • 引导研究人员在GPCR研究中选择最佳的成像和光谱方法.

主要方法:

  • 复习先进的光学显微镜技术 (例如超分辨率显微镜).
  • 探索用于探测分子动态的光谱学方法.
  • 讨论单分子检测策略.
  • 对内生系统的标签技术的分析.
  • 考虑适用于大型生物体的方法.

主要成果:

  • 最近的发展为GPCR信号机制提供了前所未有的见解.
  • 先进的技术实现了高空间和时间分辨率,使得详细的观测.
  • 单分子方法和改进的标签策略促进了对内源系统的研究.
  • 对大型生物的适用性扩大了GPCR研究的范围.

结论:

  • 光学显微镜和光谱是剖析GPCR信号的重要工具.
  • 审查的技术使研究人员能够研究复杂的细胞信号通路.
  • 这一审查有助于为GPCR研究战略选择先进的成像和光谱技术.