Liu Yu-Zhen, Chen Yan-Nan, Sun Qiang
Key Laboratory of Orogenic Belts and Crustal Evolution, Ministry of Education, The School of Earth and Space Sciences, Peking University, Beijing 100871, China.
Molecules. 2024 Jun 1;29(11):2601. doi: 10.3390/molecules29112601.
According to our recent studies on hydrophobicity, this work is aimed at understanding the dependence of hydrophobic interactions on the shape of a solute's surface. It has been observed that dissolved solutes primarily affect the structure of interfacial water, which refers to the top layer of water at the interface between the solute and water. As solutes aggregate in a solution, hydrophobic interactions become closely related to the transition of water molecules from the interfacial region to the bulk water. It is inferred that hydrophobic interactions may depend on the shape of the solute surface. To enhance the strength of hydrophobic interactions, the solutes tend to aggregate, thereby minimizing their surface area-to-volume ratio. This also suggests that hydrophobic interactions may exhibit directional characteristics. Moreover, this phenomenon can be supported by calculated potential mean forces (PMFs) using molecular dynamics (MD) simulations, where different surfaces, such as convex, flat, or concave, are associated with a sphere. Furthermore, this concept can be extended to comprehend the molecular packing parameter, commonly utilized in studying the self-assembly behavior of amphiphilic molecules in aqueous solutions.
根据我们最近关于疏水性的研究,这项工作旨在了解疏水相互作用对溶质表面形状的依赖性。据观察,溶解的溶质主要影响界面水的结构,界面水是指溶质与水界面处的顶层水。当溶质在溶液中聚集时,疏水相互作用与水分子从界面区域向本体水的转变密切相关。据推测,疏水相互作用可能取决于溶质表面的形状。为了增强疏水相互作用的强度,溶质倾向于聚集,从而使其表面积与体积之比最小化。这也表明疏水相互作用可能具有方向性特征。此外,使用分子动力学(MD)模拟计算的势能平均力(PMF)可以支持这一现象,其中不同的表面,如凸面、平面或凹面,都与一个球体相关联。此外,这一概念可以扩展到理解分子堆积参数,该参数常用于研究两亲分子在水溶液中的自组装行为。