溶剂特征的马尔科夫状态模型揭示了蛋白质-结合中的水动态
Robert M Raddi1, Vincent A Voelz1
1Department of Chemistry, Temple University, Philadelphia, Pennsylvania 19122, United States.
The journal of physical chemistry. B
|December 11, 2023
概括
这项研究揭示了溶剂分子如何影响蛋白结合,特别是与MDM2结合的p53交换活化域 (TAD). 专注于溶剂特征可以加快对这些关键分子相互作用的理解.
科学领域:
- 计算生物学 计算生物学
- 分子动力学分子动力学
- 生物物理学的生物物理.
背景情况:
- 结合p53交换活化域 (TAD) 与MDM2是一个关键的生物过程.
- 之前的工作建立了一个马尔科夫状态模型 (MSM) 这种结合反应使用广泛的显式溶剂分子模拟.
研究的目的:
- 研究溶剂分子在MDM2-p53结合反应中的特定作用.
- 开发一种以溶剂为中心的视角来研究-蛋白相互作用和疏水效应.
主要方法:
- 利用基于溶剂的结构特征的时间滞后独立成分分析 (tICA).
- 使用这些以溶剂为中心的特征构建了一个马尔科夫状态模型 (MSM).
- 可视化了关键的溶剂外及其在结合过程中的过渡.
主要成果:
- 一个基于溶剂特征的MSM揭示了一个类似于先前全原子模型的绑定景观.
- 当使用溶剂特征时,最慢运动的默认时间表被加速.
- 在p53 TAD (3-6 Å) 的Lys24和Thr18周围的溶剂外被确定为至关重要的.
结论:
- 溶剂结构为模拟蛋白结合提供了一个强大而高效的描述器.
- 这种以溶剂为中心的方法在现实的结合场景中提供了对疏水效应的见解.
- 这些发现加速了对分子识别机制的理解.
相关概念视频
Chemical Shift: Internal References and Solvent Effects
651
In an NMR sample, precise measurement of the absolute absorption frequencies of nuclei is difficult. A standard internal reference compound is added, and the frequency difference between the reference signal and sample signals is measured.
The internal reference compound generally used in NMR spectroscopy is tetramethylsilane (TMS). TMS is preferred because it is chemically inert, soluble in NMR solvents, and easily removable. Also, the highly shielded methyl protons in TMS yield an intense...
The internal reference compound generally used in NMR spectroscopy is tetramethylsilane (TMS). TMS is preferred because it is chemically inert, soluble in NMR solvents, and easily removable. Also, the highly shielded methyl protons in TMS yield an intense...
651
Noncovalent Attractions in Biomolecules
51.2K
Noncovalent attractions are associations within and between molecules that influence the shape and structural stability of complexes. These interactions differ from covalent bonding in that they do not involve sharing of electrons.
Four types of noncovalent interactions are hydrogen bonds, van der Waals forces, ionic bonds, and hydrophobic interactions.
Hydrogen bonding results from the electrostatic attraction of a hydrogen atom covalently bonded to a strong-electronegative atom like oxygen,...
Four types of noncovalent interactions are hydrogen bonds, van der Waals forces, ionic bonds, and hydrophobic interactions.
Hydrogen bonding results from the electrostatic attraction of a hydrogen atom covalently bonded to a strong-electronegative atom like oxygen,...
51.2K
Entropy and Solvation
7.1K
The process of surrounding a solute with solvent is called solvation. It involves evenly distributing the solute within the solvent. The rule of thumb for determining a solvent for a given compound is that like dissolves like. A good solvent has molecular characteristics similar to those of the compound to be dissolved. For example, polar solutions dissolve polar solutes, and apolar solvents dissolve apolar solutes. A polar solvent is a solvent that has a high dielectric constant (ϵ...
7.1K
Ligand Binding Sites
12.9K
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...
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...
12.9K
Intermolecular Forces
58.4K
Atoms and molecules interact through bonds (or forces): intramolecular and intermolecular. The forces are electrostatic as they arise from interactions (attractive or repulsive) between charged species (permanent, partial, or temporary charges) and exist with varying strengths between ions, polar, nonpolar, and neutral molecules. The different types of intermolecular forces are ion–dipole, dipole–dipole, hydrogen bonds, and dispersion; among these, dipole–dipole, hydrogen...
58.4K
Protein Folding
118.2K
Overview
118.2K


