نتایج جستجو برای: lipid bilayer

تعداد نتایج: 171427  

Journal: :The Journal of biological chemistry 2000
C van der Does J Swaving W van Klompenburg A J Driessen

To determine the phospholipid requirement of the preprotein translocase in vitro, the Escherichia coli SecYEG complex was purified in a delipidated form using the detergent dodecyl maltoside. SecYEG was reconstituted into liposomes composed of defined synthetic phospholipids, and proteoliposomes were analyzed for their preprotein translocation and SecA translocation ATPase activity. The activit...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2008
Yana K Reshetnyak Oleg A Andreev Michael Segala Vladislav S Markin Donald M Engelman

The pH low-insertion peptide (pHLIP) serves as a model system for peptide insertion and folding across a lipid bilayer. It has three general states: (I) soluble in water or (II) bound to the surface of a lipid bilayer as an unstructured monomer, and (III) inserted across the bilayer as a monomeric alpha-helix. We used fluorescence spectroscopy and isothermal titration calorimetry to study the i...

Journal: :Biophysical journal 2003
Jarrod J Buffy Teresa Hong Satoru Yamaguchi Alan J Waring Robert I Lehrer Mei Hong

The depth of insertion of an antimicrobial peptide, protegrin-1 (PG-1), in lipid bilayers is investigated using solid-state NMR. Paramagnetic Mn(2+) ions bind to the surface of lipid bilayers and induce distance-dependent dipolar relaxation of nuclear spins. By comparing the signal dephasing of the peptide with that of the lipids, whose segmental depths of insertion are known, we determined the...

2002
L. Ma N. D. Weiner

The partitioning of the n-alkyl-p-aminobenzoates into the lipid bilayer is dependent not only on their physicochemical properties, but also on temperature and bilayer composition. Partitioning studies with this homologous series demonstrate the effect of alkyl chain length on partitioning in pure DPPC liposomes at 23 and 50°C and in DPPC : Chol liposomes at 23°C. A general trend is observed whe...

2016
Huey Huang

Amphiphilic helical peptides exhibit an insertion transition when they interact with lipid bilayers. At low concentrations, the peptides adsorb at the hydrophilic-hydrophobic interface with the helical axes parallel to the bilayer surface. However, if the peptide concentration is above a critical value, a macroscopic fraction of the peptide molecules insert perpendicularly into the bilayer. The...

Journal: :Biochimica et biophysica acta 2000
E Staudegger E J Prenner M Kriechbaum G Degovics R N Lewis R N McElhaney K Lohner

We have investigated the effect of the interaction of the antimicrobial peptide gramicidin S (GS) on the thermotropic phase behavior of model lipid bilayer membranes generated from the total membrane lipids of Acholeplasma laidlawii B and Escherichia coli. The A. laidlawii B membrane lipids consist primarily of neutral glycolipids and anionic phospholipids, while the E. coli inner membrane lipi...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1995
J L Soulages Z Salamon M A Wells G Tollin

The binding of the exchangeable apolipoprotein apolipophorin III (apoLp-III) to an egg phosphatidylcholine bilayer as a function of the concentration of diacylglycerol (DG) in the bilayer was studied by surface plasmon resonance spectroscopy. At a DG concentration of 2 mol % in the bilayer, the binding of apoLp-III reached saturation. Under saturating conditions, apoLp-III forms a closely packe...

2016
Susanne Heider John A Dangerfield Christoph Metzner

Glycosylphosphatidylinositol (GPI)-anchored proteins (GPI-APs) use a unique posttranslational modification to link proteins to lipid bilayer membranes. The anchoring structure consists of both a lipid and carbohydrate portion and is highly conserved in eukaryotic organisms regarding its basic characteristics, yet highly variable in its molecular details. The strong membrane targeting property h...

Journal: :Biophysical journal 2014
Alexander Kyrychenko J Alfredo Freites Jing He Douglas J Tobias William C Wimley Alexey S Ladokhin

We use a number of computational and experimental approaches to investigate the membrane topology of the membrane-interacting C-terminal domain of the HIV-1 gp41 fusion protein. Several putative transmembrane regions are identified using hydrophobicity analysis based on the Wimley-White scales, including the membrane-proximal external region (MPER). The MPER region is an important target for ne...

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