about
Carbon dioxide transport through membranesAquaporin-1, nothing but a water channel.Changes of the membrane potential profile induced by verapamil and propranolol.High-speed AFM images of thermal motion provide stiffness map of interfacial membrane protein moietiesWater Determines the Structure and Dynamics of Proteins.Electrostatically induced recruitment of membrane peptides into clusters requires ligand binding at both interfacesMembrane destabilization by ricin.A critical reassessment of penetratin translocation across lipid membranesHighly selective water channel activity measured by voltage clamp: analysis of planar lipid bilayers reconstituted with purified AqpZ.Water and ion permeation of aquaporin-1 in planar lipid bilayers. Major differences in structural determinants and stoichiometry.Monitoring single-channel water permeability in polarized cells.Routes of epithelial water flow: aquaporins versus cotransporters.Fast and selective ammonia transport by aquaporin-8.Protons migrate along interfacial water without significant contributions from jumps between ionizable groups on the membrane surfaceThe mobility of single-file water molecules is governed by the number of H-bonds they may form with channel-lining residues.Uroplakins do not restrict CO2 transport through urothelium.Combined transport of water and ions through membrane channels.Voltage-sensitive styryl dyes as singlet oxygen targets on the surface of bilayer lipid membrane.Water at hydrophobic interfaces delays proton surface-to-bulk transfer and provides a pathway for lateral proton diffusion.The Sodium Glucose Cotransporter SGLT1 Is an Extremely Efficient Facilitator of Passive Water TransportFilter gate closure inhibits ion but not water transport through potassium channelsNo facilitator required for membrane transport of hydrogen sulfide.Beyond the diffusion limit: Water flow through the empty bacterial potassium channel.Real-time monitoring of membrane-protein reconstitution by isothermal titration calorimetry.110 years of the Meyer-Overton rule: predicting membrane permeability of gases and other small compounds.Protons and Hydroxide Ions in Aqueous Systems.The size of the unstirred layer as a function of the solute diffusion coefficient.Dehydration of model membranes induced by lectins from Ricinus communis and Viscum album.Solvent drag across gramicidin channels demonstrated by microelectrodes.Photosensitizer binding to lipid bilayers as a precondition for the photoinactivation of membrane channels.Membrane photopotential generation by interfacial differences in the turnover of a photodynamic reaction.Desformylgramicidin: a model channel with an extremely high water permeability.Water permeation through gramicidin A: desformylation and the double helix: a molecular dynamics study.Structural proton diffusion along lipid bilayers.Cyclic AMP is sufficient for triggering the exocytic recruitment of aquaporin-2 in renal epithelial cellsOrigin of proton affinity to membrane/water interfacesThe bacterial translocon SecYEG opens upon ribosome binding.Design of peptide-membrane interactions to modulate single-file water transport through modified gramicidin channels.Local partition coefficients govern solute permeability of cholesterol-containing membranes.Invariance of single-file water mobility in gramicidin-like peptidic pores as function of pore length.
P50
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P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Peter Pohl
@ast
Peter Pohl
@br
Peter Pohl
@co
Peter Pohl
@cs
Peter Pohl
@da
Peter Pohl
@de
Peter Pohl
@en
Peter Pohl
@es
Peter Pohl
@fr
Peter Pohl
@id
type
label
Peter Pohl
@ast
Peter Pohl
@br
Peter Pohl
@co
Peter Pohl
@cs
Peter Pohl
@da
Peter Pohl
@de
Peter Pohl
@en
Peter Pohl
@es
Peter Pohl
@fr
Peter Pohl
@id
prefLabel
Peter Pohl
@ast
Peter Pohl
@br
Peter Pohl
@co
Peter Pohl
@cs
Peter Pohl
@da
Peter Pohl
@de
Peter Pohl
@en
Peter Pohl
@es
Peter Pohl
@fr
Peter Pohl
@id
P1053
A-5361-2008
P106
P1153
7101941342
P21
P31
P3829
P496
0000-0002-1792-2314