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相关概念视频

Ligand Binding Sites02:40

Ligand Binding Sites

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Proteins are dynamic macromolecules that carry out a wide variety of essential processes; however, the activities of most proteins depend on their interactions with other molecules or ions, known as ligands.
Protein-ligand interactions are quite specific; even though numerous potential ligands surround a cellular protein at any given time, only a particular ligand can bind to that protein. Moreover, a ligand binds only to a dedicated area on the surface of the protein, known as the...
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Conserved Binding Sites01:49

Conserved Binding Sites

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Many proteins’ biological role depends on their interactions with their ligands, small molecules that bind to specific locations on the protein known as ligand-binding sites. Ligand-binding sites are often conserved among homologous proteins as these sites are critical for protein function.
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally...
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Cooperative Allosteric Transitions01:58

Cooperative Allosteric Transitions

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Cooperative allosteric transitions can occur in multimeric proteins, where each subunit of the protein has its own ligand-binding site. When a ligand binds to any of these subunits, it triggers a conformational change that affects the binding sites in the other subunits; this can change the affinity of the other sites for their respective ligands. The ability of the protein to change the shape of its binding site is attributed to the presence of a mix of flexible and stable segments in the...
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Protein-protein Interfaces02:04

Protein-protein Interfaces

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Many proteins form complexes to carry out their functions, making protein-protein interactions (PPIs) essential for an organism's survival. Most PPIs are stabilized by numerous weak noncovalent chemical forces. The physical shape of the interfaces determines the way two proteins interact. Many globular proteins have closely-matching shapes on their surfaces, which form a large number of weak bonds. Additionally, many PPIs occur between two helices or between a surface cleft and a...
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Induced-fit Model01:13

Induced-fit Model

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Most chemical reactions in cells require enzymes—biological catalysts that speed up the reaction without being consumed or permanently changed. They reduce the activation energy needed to convert the reactants into products. Enzymes are proteins, that usually work by binding to a substrate—a reactant molecule that they act upon.
Enzymes exhibit substrate specificity, meaning that they can only bind to certain substrates. This is mainly determined by the shape and chemical...
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Protein Folding01:25

Protein Folding

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Proteins are chains of amino acids linked together by peptide bonds. Upon synthesis, a protein folds into a three-dimensional conformation, critical to its biological function. Interactions between its constituent amino acids guide protein folding, and hence the protein structure is primarily dependent on its amino acid sequence.
Protein Structure Is Critical to Its Biological Function
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Protein WISDOM: A Workbench for In silico De novo Design of BioMolecules
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脂质-蛋白质结合中的反向合规选择

Amélie Bacle1, Pavel Buslaev2,3, Rebeca Garcia-Fandino4,5

  • 1Laboratoire Coopératif "Lipotoxicity and Channelopathies - ConicMeds", Université de Poitiers, 1 rue Georges Bonnet, Poitiers 86000, France.

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概括

脂质头组表现出各种各样的形状,而不仅仅是一些刚性结构. 这种形状的灵活性使脂质能够有效地与各种生物分子结合,包括蛋白质,RNA和药物.

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科学领域:

  • 生物化学和纳米生物技术
  • 分子生物物理学

背景情况:

  • 膜和纳米颗粒上的脂质头组与生物分子相互作用.
  • 对于纳米生物技术 (例如mRNA疫苗载体) 等领域来说,了解脂质头组构造至关重要.
  • 之前的研究缺乏在生理条件下对脂质头组构成组的实验数据.

研究的目的:

  • 在生物相关条件下确定主要脂质组的构造组.
  • 调查脂质组是否采用一些刚性结构或连续的结构谱.
  • 探索脂质群灵活性对生物分子相互作用的影响.

主要方法:

  • 结合固态核磁共振 (NMR) 实验和分子动力学 (MD) 模拟 (NMR脂质项目).
  • 在各种条件下分析了四种主要的脂类.
  • 从蛋白质数据库 (PDB) 检查了894个与蛋白质结合的脂质结构.

主要成果:

  • 脂质组在中性和带电膜中采样了广泛的重叠形状.
  • 头组化学影响着形状的概率分布,而不是范围本身.
  • 脂质结合不同形状的蛋白质,不管头组的化学成分如何.

结论:

  • 脂质组具有广泛的形状灵活性.
  • 脂质利用这种灵活性来选择合适的构造以结合不同蛋白位点.
  • 拟议的逆形状选择模型适用于与蛋白质,药物,RNA和病毒的脂质相互作用.