articleTop 1% cited
Hydrophobicity at Small and Large Length Scales
The Journal of Physical Chemistry B · 1999 · Vol. 103(22) · pp. 4570–4577
Ka Lum✉(University of California, Berkeley)David Chandler(University of California, Berkeley)John D. Weeks(University of Maryland, College Park)
Abstract
We develop a unified and generally applicable theory of solvation of small and large apolar species in water. In the former, hydrogen bonding of water is hindered yet persists near the solutes. In the latter, hydrogen bonding is depleted, leading to drying of extended apolar surfaces, large forces of attraction, and hysteresis on mesoscopic length scales. The crossover occurs on nanometer length scales, when the local concentration of apolar units is sufficiently high, or when an apolar surface is sufficiently large. Our theory for the crossover has implications concerning the stability of protein assemblies and protein folding.
Protein Structure and DynamicsEnzyme Structure and FunctionPhase Equilibria and ThermodynamicsMesoscopic physicsChemical physicsCrossoverSolvationHydrogen bondFolding (DSP implementation)Length scaleHysteresisChemistryStatistical physics
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References
The Hydrophobic Effect: Formation of Micelles and Biological Membranes
FEBS Letters · 1981 · 2,708 citations
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