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相关概念视频

Ligand Binding and Linkage00:49

Ligand Binding and Linkage

Allosteric proteins have more than one ligand binding site; the binding of a ligand to any of these sites influences the binding of ligands to the other sites. When a protein is allosteric, its binding sites are called coupled or linked.  In the case of enzymes, the site that binds to the substrate is known as the active site and the other site is known as the regulatory site. When a ligand binds to the regulatory site, this leads to conformational changes in the protein that can influence the...
Cooperative Binding of Transcription Regulators02:13

Cooperative Binding of Transcription Regulators

Transcriptional regulators bind to specific cis-regulatory sequences in the DNA to regulate gene transcription. These cis-regulatory sequences are very short, usually less than ten nucleotide pairs in length. The short length means that there is a high probability of the exact same sequence randomly occurring throughout the genome.  Since regulators can also bind to groups of similar sequences, this further increases the chances of random binding. Transcriptional regulators form dimers that...
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...
Complexation Equilibria: The Chelate Effect01:19

Complexation Equilibria: The Chelate Effect

In complexation reactions, metal atoms or cations interact with ligands to form donor-acceptor adducts called metal complexes. Ligands that bind through one donor site are monodentate, ligands with two donor sites are bidentate, and those with more than two donor sites are polydentate ligands. For example, ethylene diamine is a bidentate ligand that binds through two nitrogen donor atoms, forming a five-membered ring. EDTA is a polydentate ligand that binds through four oxygen and two nitrogen...
Complexometric Titration: Ligands00:43

Complexometric Titration: Ligands

Different monodentate and polydentate ligands are used as complexing agents in complexometric titration reactions. The formation of complexes by mono- and bidentate ligands involves two or more intermediate steps, limiting their use as complexing agents. In comparison, polydentate ligands can form complexes with metal ions in a single-step process, facilitating sharper end points. This means polydentate ligands, such as amino carboxylic acid derivatives, are most commonly employed in...

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相关实验视频

Updated: Jul 16, 2026

Real Time Measurements of Membrane Protein:Receptor Interactions Using Surface Plasmon Resonance (SPR)
09:35

Real Time Measurements of Membrane Protein:Receptor Interactions Using Surface Plasmon Resonance (SPR)

Published on: November 29, 2014

聚合物长度对多重联体受体键形成的影响.

C Jeppesen1, J Y Wong, T L Kuhl

  • 1Materials Research Laboratory, Department of Chemical Engineering, University of California, Santa Barbara, CA 93106, USA.

Science (New York, N.Y.)
|July 21, 2001
PubMed
概括

细胞粘附效率依赖于罕见的延长聚合物链形状,而不仅仅是分子结合特性. 这一发现影响了对细胞相互作用和生物材料的理解.

科学领域:

  • 生物物理学的生物物理.
  • 材料科学 材料科学 材料科学
  • 细胞生物学 细胞生物学

背景情况:

  • 细胞粘附是由灵活的带上的连接体介导的,它们与表面受体结合.
  • 了解这些带的动态对于细胞相互作用研究至关重要.

研究的目的:

  • 量化聚合物链动力学和联体受体结合动力学.
  • 为了确定绑定的连接体-受体相互作用的空间范围和效率.

主要方法:

  • 蒙特卡罗模拟的蒙特卡罗模拟
  • 扩散反应理论 扩散反应理论
  • 测量表面力 (生物素 - 斯特雷普塔维丁系统)

主要成果:

  • 测量了聚合物链动力学和结合动力学.
  • 结合效率取决于罕见的,扩展的聚合物形状.
  • 分子架构和平衡束配置不如罕见的构造那么重要.

结论:

  • 聚合物的"罕见"扩展形状是有效的细胞粘附的关键.
  • 这为细胞表面分子相互作用的生物物理学提供了新的见解.

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Co-Translational Insertion of Membrane Proteins into Preformed Nanodiscs
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Co-Translational Insertion of Membrane Proteins into Preformed Nanodiscs

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The Development and Application of Biophysical Assays for Evaluating Ternary Complex Formation Induced by Proteolysis Targeting Chimeras (PROTACS)
07:22

The Development and Application of Biophysical Assays for Evaluating Ternary Complex Formation Induced by Proteolysis Targeting Chimeras (PROTACS)

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相关实验视频

Last Updated: Jul 16, 2026

Real Time Measurements of Membrane Protein:Receptor Interactions Using Surface Plasmon Resonance (SPR)
09:35

Real Time Measurements of Membrane Protein:Receptor Interactions Using Surface Plasmon Resonance (SPR)

Published on: November 29, 2014

Co-Translational Insertion of Membrane Proteins into Preformed Nanodiscs
08:24

Co-Translational Insertion of Membrane Proteins into Preformed Nanodiscs

Published on: November 19, 2020

The Development and Application of Biophysical Assays for Evaluating Ternary Complex Formation Induced by Proteolysis Targeting Chimeras (PROTACS)
07:22

The Development and Application of Biophysical Assays for Evaluating Ternary Complex Formation Induced by Proteolysis Targeting Chimeras (PROTACS)

Published on: January 12, 2024