Enhancing the Hydrophobic Effect in Confined Water Nanodrops
- 10 November 2007
- journal article
- research article
- Published by American Chemical Society (ACS) in Langmuir
- Vol. 23 (26) , 12795-12798
Abstract
The distribution of hydrophobic solutes, such as methane, enclosed in a nanosized water droplet contained in a reverse micelle of diameter 2.82 nm is investigated using Monte Carlo simulations. The effect of the hydrophobic solute's atomic diameter on the solute-solute potential of mean force is also studied. The study reveals that confinement has a strong influence on the solute's tendency to associate. The potential of mean force exhibits only a single minimum, indicating that the contact pair is the only stable configuration between solutes. The solvent-separated pair that is universally observed for small solutes in bulk water is conspicuously absent. This enhanced hydrophobic effect is attributed to the lack of sufficient water to completely hydrate and stabilize the solvent-separated configurations. The study is expected to be important in understanding the role of hydrophobic forces during protein folding and nucleation under confinement.Keywords
This publication has 22 references indexed in Scilit:
- Effects of Crowding and Confinement on the Structures of the Transition State Ensemble in ProteinsThe Journal of Physical Chemistry B, 2007
- Protein folding under confinement: A role for solventProceedings of the National Academy of Sciences, 2007
- Effects of lengthscales and attractions on the collapse of hydrophobic polymers in waterProceedings of the National Academy of Sciences, 2007
- Hydrophobic and Ionic Interactions in Nanosized Water DropletsJournal of the American Chemical Society, 2006
- Interfaces and the driving force of hydrophobic assemblyNature, 2005
- Pressure-Induced Protein Unfolding in the Ternary System AOT−Octane−Water Is Different from that in Bulk WaterLangmuir, 2005
- Direct Refolding of Inclusion Bodies Using Reversed MicellesBiotechnology Progress, 2004
- Forced Folding and Structural Analysis of Metastable ProteinsJournal of the American Chemical Society, 2004
- The hydrophobic effectPhysical Chemistry Chemical Physics, 2003
- The influence of temperature on pairwise hydrophobic interactions of methane-like particles: A molecular dynamics study of free energyThe Journal of Chemical Physics, 1996