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相关概念视频

The Equilibrium Binding Constant and Binding Strength02:18

The Equilibrium Binding Constant and Binding Strength

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The equilibrium binding constant (Kb) quantifies the strength of a protein-ligand interaction. Kb can be calculated as follows when the reaction is at equilibrium:
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Calculating Standard Free Energy Changes02:49

Calculating Standard Free Energy Changes

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The free energy change for a reaction that occurs under the standard conditions of 1 bar pressure and at 298 K is called the standard free energy change. Since free energy is a state function, its value depends only on the conditions of the initial and final states of the system. A convenient and common approach to the calculation of free energy changes for physical and chemical reactions is by use of widely available compilations of standard state thermodynamic data. One method involves the...
22.2K
An Introduction to Free Energy01:05

An Introduction to Free Energy

9.0K
How can we compare the energy that releases from one reaction to that of another reaction? We use a measurement of free energy to quantitate these energy transfers. Scientists call this free energy Gibbs free energy (abbreviated with the letter G) after Josiah Willard Gibbs, the scientist who developed the measurement. According to the second law of thermodynamics, all energy transfers involve losing some energy in an unusable form such as heat, resulting in entropy. Gibbs free energy...
9.0K
Nuclear Binding Energy02:13

Nuclear Binding Energy

13.2K
The difference between the calculated and experimentally measured masses is known as the mass defect of the atom. In the case of helium-4, the mass defect indicates a “loss” in mass of 4.0331 amu – 4.0026 amu = 0.0305 amu. The loss in mass accompanying the formation of an atom from protons, neutrons, and electrons is due to the conversion of that mass into energy that is evolved as the atom forms. The nuclear binding energy is the energy produced when the atoms’ nucleons...
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Conserved Binding Sites01:49

Conserved Binding Sites

4.4K
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...
4.4K
Arrhenius Plots02:34

Arrhenius Plots

41.4K
The Arrhenius equation relates the activation energy and the rate constant, k, for chemical reactions. In the Arrhenius equation, k = Ae−Ea/RT, R is the ideal gas constant, which has a value of 8.314 J/mol·K, T is the temperature on the kelvin scale, Ea is the activation energy in J/mole, e is the constant 2.7183, and A is a constant called the frequency factor, which is related to the frequency of collisions and the orientation of the reacting molecules.
The Arrhenius equation can be used...
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相关实验视频

Updated: Sep 19, 2025

Quantitative Structure-Activity Relationship, Activity Prediction, and Molecular Dynamics of Non-nucleotide Reverse Transcriptase Inhibitors
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一种正式准确的方法,用于计算高通量绝对无约束的自由能量.

Hengwei Bian1,2, Xueguang Shao1,2, Christophe Chipot3,4,5

  • 1Research Center for Analytical Sciences, Tianjin Key Laboratory of Biosensing and Molecular Recognition, State Key Laboratory of Medicinal Chemical Biology, College of Chemistry, Nankai University, Tianjin, China.

Nature computational science
|June 18, 2025
PubMed
概括

我们开发了一种更快,更准确的方法来计算蛋白质和连接体中的结合自由能量. 这种计算方法显著提高了药物发现和化学研究的效率和可靠性.

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Protein WISDOM: A Workbench for In silico De novo Design of BioMolecules
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Measuring Biomolecular DSC Profiles with Thermolabile Ligands to Rapidly Characterize Folding and Binding Interactions
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Protein WISDOM: A Workbench for In silico De novo Design of BioMolecules
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科学领域:

  • 计算化学是一种计算化学.
  • 分子建模分子建模
  • 生物物理学的生物物理.

背景情况:

  • 准确计算结合的自由能量对于药物发现至关重要.
  • 传统方法在计算效率和准确性方面面临挑战.
  • 蛋白质 - 配体相互作用是复杂的,需要精确的建模.

研究的目的:

  • 引入一种高通量,形式精确的方法,用于绝对具有约束力的自由能量计算.
  • 提高分子结合研究的计算效率和准确性.
  • 提高预测药物开发中的结合亲和关系的可靠性.

主要方法:

  • 利用了一种新的热力学循环,最大限度地减少了蛋白质 - 连接体相对运动.
  • 实施双宽采样和质量再分配以提高效率.
  • 适用于柔性联体的潜在平均力计算.

主要成果:

  • 与传统方法相比,实现了八倍的效率提升.
  • 在34个复合体中,被证明的平均无标记误差<1kcal/mol和歇斯底里<0.5kcal/mol.
  • 成功建模了灵活的配体,计算开销最小 (<5%).

结论:

  • 开发的方法为具有约束力的自由能源计算提供了显著的效率和准确性的改进.
  • 这种方法为各种蛋白质-连接体复合体提供了特殊的可靠性.
  • 该方法有可能促进物理,生物和药物化学领域的研究.