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相关概念视频

Eukaryotic Transcription Inhibitors01:52

Eukaryotic Transcription Inhibitors

Certain biochemical processes, such as embryonic development and cell growth regulation, depend on the repression of specific genes. DNA binding proteins known as eukaryotic transcription inhibitors regulate the repression of gene expression in eukaryotes. The presence of these inhibitors at the required location and time in the cell is triggered by the presence of hormones and additional signals from other cells.
Eukaryotic transcription inhibitors usually contain two distinct domains, a DNA...
Activation and Inactivation of G Proteins01:22

Activation and Inactivation of G Proteins

Heterotrimeric G proteins are guanine nucleotide-binding proteins. As the name suggests, heterotrimeric G proteins are composed of three subunits: alpha, beta, and gamma. They remain GDP-bound or GTP-bound inside the cells and switch between inactive/active states. The Gα subunit possesses the nucleotide-binding pocket that binds guanine nucleotides and switches between GDP or GTP-bound states. In contrast, the Gꞵ and Gγ subunits are always bound together with high affinity and are together...
GPCR Desensitization01:12

GPCR Desensitization

G protein-coupled receptor (GPCR) signaling plays a crucial role in cell functioning. GPCR desensitization is an equally essential process. It allows cells to respond to changing environments and regain sensitivity to new stimuli while preventing unnecessary stimulation when no longer needed. Prolonged exposure to stimuli leads to GPCR desensitization. It involves blocking the receptors from binding and activating additional G proteins. This inhibits activation of downstream effectors, thereby...
Transducer Mechanism: G Protein–Coupled Receptors01:30

Transducer Mechanism: G Protein–Coupled Receptors

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, 7TM, or...

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Updated: Jun 14, 2026

A G-quadruplex DNA-affinity Approach for Purification of Enzymatically Active G4 Resolvase1
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超特定的G-四重体-胆固醇相互作用以实现高效的全转录组G4映射

Shijiong Wei1, Xiaobo Zhang1, Yilong Feng2

  • 1State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, China.

Journal of the American Chemical Society
|March 6, 2025
PubMed
概括

抗生素胆固醇 (COL) 特别结合并行的G四重复体 (G4s),导致它们聚合. 这一发现使 CoRP-seq 的开发成为可能,这是一种简单的方法来绘制人体细胞中的 RNA G4s.

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科学领域:

  • 化学生物学
  • 基因组学
  • 分子生物学

背景情况:

  • G四重复体 (G4s) 是具有动态多态性的复杂核酸结构,对化学生物学干预构成挑战.
  • 针对G4s对于理解细胞过程和开发新疗法至关重要.

研究的目的:

  • 研究小分子与特定G4结构的相互作用.
  • 开发一种用于评估人类转录组中RNAG四重复的新方法.

主要方法:

  • 利用抗生素胆固醇 (COL) 与平行G四重复体 (G4s) 之间的特定相互作用.
  • 开发了COL诱导的RNA G4沉和测序 (CoRP-seq) 协议,使用结构特异的聚合和离心方法进行G4隔离.
  • 应用 CoRP-seq 来评估人类细胞转录组中的 RNA G4 流行率.

主要成果:

  • 素 (COL) 选择性地与平行G四重复体 (G4s) 结合.
  • 这种特定的相互作用会诱导G4/COL复合体的聚合,从而通过离心法进行分离.
  • CoRP-seq协议显示了超特异性,简单性和用于绘制RNA G4s的便利性.

结论:

  • 发现COL的特定G4相互作用为G4向提供了一个新的工具.
  • CoRP-seq提供了一种简单且高度特异性的RNA G-四重复性分析方法.
  • 这一进步解决了G4映射和G4omics更广泛领域的未满足需求.