Hydrophobic interactions drive the binding of
nonpolar ligands to the oily pockets of proteins and supramolecular
species in aqueous solution. As such, the wetting of host
pockets is expected to play a critical role in determining the
thermodynamics of guest binding. Here we use molecular
simulations to examine the impact of pressure on the wetting
and dewetting of the nonpolar pockets of a series of deep-cavity
cavitands in water. The portals to the cavitand pockets are
functionalized with both nonpolar (methyl) and polar (hydroxyl)
groups oriented pointing either upward or inward toward the
pocket. We find wetting of the pocket is favored by the hydroxyl
groups and dewetting is favored by the methyl groups. The
distribution of waters in the pocket is found to exhibit a two-state-like equilibrium between wet and dry states with a free energy
barrier between the two states. Moreover, we demonstrate that the pocket hydration of the cavitands can be collapsed onto a unified
adsorption isotherm by assuming the effective pressures within each cavitand pocket differ by a shift pressure that depends on the
chemical identity and number of functional groups placed about the portal. These observations support the development of a twostate
capillary evaporation model that accurately describes the equilibrium between states and naturally gives rise to the effective shift
pressures observed from simulation. This work demonstrates that the hydration of host pockets can be tuned following simple design
rules that in turn are expected to impact the thermodynamics of guest complexation.
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Spontaneous drying of non-polar deep-cavity cavitand pockets in aqueous solution
There are many open questions regarding the hydration of solvent-exposed, non-polar tracts and pockets in proteins. Although water is predicted to de-wet purely repulsive surfaces and evacuate crevices, the extent of de-wetting is unclear when ubiquitous van der Waals interactions are in play. The structural simplicity of synthetic supramolecular hosts imbues them with considerable potential to address this issue. To this end, here we detail a combination of densimetry and molecular dynamics simulations of three cavitands, coupled with calorimetric studies of their complexes with short-chain carboxylates. Our results reveal the range of wettability possible within the ostensibly identical cavitand pockets — which differ only in the presence/position of the methyl groups that encircle the portal to their non-polar pockets. The results demonstrate the ability of macrocycles to template water cavitation within their binding sites and show how the orientation of methyl groups can trigger the drying of non-polar pockets in liquid water, suggesting new avenues to control guest complexation.
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- PAR ID:
- 10156072
- Date Published:
- Journal Name:
- Nature Chemistry
- ISSN:
- 1755-4330
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
-
Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1038/s41557-020-0458-8
