AbstractThe aquaglyceroporins of Escherichia coli, EcGlpF, and of Plasmodium falciparum, PfAQP, are probably the best characterized members of the solute-conducting aquaporin (AQP) subfamily. Their crystal structures have been elucidated and numerous experimental and theoretical analyses have been conducted. However, opposing reports on their rates of water permeability require clarification. Hence, we expressed EcGlpF and PfAQP in yeast, prepared protoplasts, and compared water and glycerol permeability of both aquaglyceroporins in the presence of different osmolytes, i.e. sucrose, sorbitol, PEG300, and glycerol. We found that water permeability of PfAQP strongly depends on the external osmolyte, with full inhibition by sorbitol, and incre...
The water permeability of aquaporins (AQPs) varies by more than an order of magnitude even though th...
Water and glycerol permeation via human AQP3 are described exploiting advanced metadynamics approach...
AbstractWater permeation and electrostatic interactions between water and channel are investigated i...
The selectivity of aquaporins for water and solutes is determined by pore diameter. Paradoxically, t...
A large family of membrane channel proteins selective for transport of water (aquaporins) or water p...
Aquaporins are homotetrameric channel proteins, which allow the diffusion of water and small solutes...
AbstractAmong aquaglyceroporins that transport both water and glycerol across the cell membrane, Esc...
The aquaporin family of molecular water channels is widely expressed throughout the plant and animal...
SummaryThe recent availability of high-resolution structures of two structurally highly homologous, ...
AbstractFrom equilibrium molecular dynamics simulations we have determined single-channel water perm...
Aquaporins (AQPs) are a ubiquitous family of transmembrane water channel proteins. A subgroup of AQP...
The aquaglyceroporin from Plasmodium falciparum (PfAQP) is a potential drug target for the treatment...
The aquaglyceroporin AQP7, a family member of aquaporin membrane channels, facilitates the permeatio...
AbstractThe aquaglyceroporin of Plasmodium falciparum (PfAQP) is a bi-functional channel with permea...
AbstractThe aquaglyceroporin GlpF is a transmembrane channel of Escherichia coli that facilitates th...
The water permeability of aquaporins (AQPs) varies by more than an order of magnitude even though th...
Water and glycerol permeation via human AQP3 are described exploiting advanced metadynamics approach...
AbstractWater permeation and electrostatic interactions between water and channel are investigated i...
The selectivity of aquaporins for water and solutes is determined by pore diameter. Paradoxically, t...
A large family of membrane channel proteins selective for transport of water (aquaporins) or water p...
Aquaporins are homotetrameric channel proteins, which allow the diffusion of water and small solutes...
AbstractAmong aquaglyceroporins that transport both water and glycerol across the cell membrane, Esc...
The aquaporin family of molecular water channels is widely expressed throughout the plant and animal...
SummaryThe recent availability of high-resolution structures of two structurally highly homologous, ...
AbstractFrom equilibrium molecular dynamics simulations we have determined single-channel water perm...
Aquaporins (AQPs) are a ubiquitous family of transmembrane water channel proteins. A subgroup of AQP...
The aquaglyceroporin from Plasmodium falciparum (PfAQP) is a potential drug target for the treatment...
The aquaglyceroporin AQP7, a family member of aquaporin membrane channels, facilitates the permeatio...
AbstractThe aquaglyceroporin of Plasmodium falciparum (PfAQP) is a bi-functional channel with permea...
AbstractThe aquaglyceroporin GlpF is a transmembrane channel of Escherichia coli that facilitates th...
The water permeability of aquaporins (AQPs) varies by more than an order of magnitude even though th...
Water and glycerol permeation via human AQP3 are described exploiting advanced metadynamics approach...
AbstractWater permeation and electrostatic interactions between water and channel are investigated i...