W
Winfried Haase
Researcher at Max Planck Society
Publications - 121
Citations - 5593
Winfried Haase is an academic researcher from Max Planck Society. The author has contributed to research in topics: Membrane protein & Receptor. The author has an hindex of 40, co-authored 121 publications receiving 5475 citations. Previous affiliations of Winfried Haase include University of Giessen.
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A high yield preparation for rat kidney brush border membranes Different behaviour of lysosomal markers
TL;DR: Rat kidney cortex slices were homogenized with a polytron in a isoosmotic medium containing 5 mmol/l EGTA and by SDS-polyacrylamide gel electrophoresis, no differences in the protein patterns were observed.
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Three-dimensional structure of the bacterial protein-translocation complex SecYEG
TL;DR: The three-dimensional map, calculated from two-dimensional SecYEG crystals, reveals a sandwich of two membranes interacting through the extensive cytoplasmic domains, which may represent the closed state of the protein-conducting channel.
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Effect of inositol-1,4,5-trisphosphate on isolated subcellular fractions of rat pancreas
TL;DR: The data suggest that inositol-1,4,5-trisphosphate releases Ca2+ from endoplasmic reticulum in pancreatic acinar cells, suggesting that IP3 might provide the missing link between activation of the muscarinic receptor and Ca1+ release from intracellular stores during stimulation.
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Studies on the orientation of brush-border membrane vesicles
TL;DR: It is shown that the brush-border membrane vesicles isolated from rat kidney cortex and from rat small intestine for transport studies are predominantly orientated right-side out.
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Evaluation of detergents for the soluble expression of α-helical and β-barrel-type integral membrane proteins by a preparative scale individual cell-free expression system
TL;DR: The cell‐free expression of three structurally very different membrane proteins, namely the bacterial α‐helical multidrug transporter, EmrE, the β‐barrel nucleoside transporter, Tsx, and the porcine vasopressin receptor of the eukaryotic superfamily of G‐protein coupled receptors is analyzed.