Nanoscale solvent confinement at the protein-water interface promotes dipole orientations that are not aligned with the internal electrostatic field of a protein, yielding what we term epistructural polarization. To quantify this effect, an equation is derived from first principles relating epistructural polarization with the magnitude of local distortions in water coordination causative of interfacial tension. The equation defines a nanoscale electrostatic model of water and enables an estimation of protein denaturation free energies and the inference of hot spots for protein associations. The theoretical results are validated vis-à-vis calorimetric data, revealing the destabilizing effect of epistructural polarization and its molecular or...
Additional resources and features associated with this article are available within the HTML version...
Nanoconfined water and aqueous solutions play a prominent role in nature and technological applicati...
The mechanisms of cold and pressure denaturation of proteins are matter of debate and are commonly u...
Nanoscale solvent confinement at the protein-water interface promotes dipole orientations that are n...
A significant episteric (around a solid) distortion of the hydrogen-bond structure of water is promo...
The topographical and physico-chemical complexity of protein-water interfaces scales down to the sub...
A net dipole moment is shown to arise from a non-Debye component of water polarization created by na...
A variational principle governing nanoscale water configurations at biological interfaces is derived...
Epistructural tension is the reversible work per unit area required to span the aqueous interface of...
The dielectric response of bulk water follows laws of continuum electrostatics,a scheme often extrap...
AbstractThe proper estimation of the influence of the many-body dynamic solvent microstructure on a ...
Building upon a non-Debye multiscale treatment of water dielectrics, this work reveals the biochemic...
The epistructural tension of a soluble protein is defined as the reversible work per unit area requi...
Since the time of Kirkwood, observed deviations in magnitude of the dielectric constant of aqueous p...
The interfacial tension of biological water, a promoter of biomolecular interactions, is difficult t...
Additional resources and features associated with this article are available within the HTML version...
Nanoconfined water and aqueous solutions play a prominent role in nature and technological applicati...
The mechanisms of cold and pressure denaturation of proteins are matter of debate and are commonly u...
Nanoscale solvent confinement at the protein-water interface promotes dipole orientations that are n...
A significant episteric (around a solid) distortion of the hydrogen-bond structure of water is promo...
The topographical and physico-chemical complexity of protein-water interfaces scales down to the sub...
A net dipole moment is shown to arise from a non-Debye component of water polarization created by na...
A variational principle governing nanoscale water configurations at biological interfaces is derived...
Epistructural tension is the reversible work per unit area required to span the aqueous interface of...
The dielectric response of bulk water follows laws of continuum electrostatics,a scheme often extrap...
AbstractThe proper estimation of the influence of the many-body dynamic solvent microstructure on a ...
Building upon a non-Debye multiscale treatment of water dielectrics, this work reveals the biochemic...
The epistructural tension of a soluble protein is defined as the reversible work per unit area requi...
Since the time of Kirkwood, observed deviations in magnitude of the dielectric constant of aqueous p...
The interfacial tension of biological water, a promoter of biomolecular interactions, is difficult t...
Additional resources and features associated with this article are available within the HTML version...
Nanoconfined water and aqueous solutions play a prominent role in nature and technological applicati...
The mechanisms of cold and pressure denaturation of proteins are matter of debate and are commonly u...