Literature DB >> 8605157

Gramicidin A aggregation in supported gel state phosphatidylcholine bilayers.

J Mou1, D M Czajkowsky, Z Shao.   

Abstract

Using an atomic force microscope, supported bilayers of saturated phosphatidylcholine (in the gel state) containing various amounts of gramicidin A (gA) were imaged in aqueous solutions and at room temperature. gA clusters were directly observed for the first time under these conditions. It was found that, at a lower gA concentration, gA aggregated into domains, composed of small clusters along with a considerable amount of lipids. This basic aggregation unit, most likely a hexamer, remained the same for acyl chain lengths from 14 to 18 carbons. These small clusters were observed to form elongated aggregates (line type) but never into extended pure gA domains. When gA concentrations were increased, for bilayers with 16 carbons or less, gA aggregated into larger domains but the basic unit remained separated by lipid molecules. At about 5 mol % gA, a percolation-like transition occurred at which the line type aggregates were connected to each other. However, for bilayers with more than 16 carbons, multiple lamellar structures were formed at higher gA fractions and the top layer had a ripple-like surface morphology. The molecular mechanism for the formation of these peculiar structures remains to be elucidated.

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Year:  1996        PMID: 8605157     DOI: 10.1021/bi9520242

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  21 in total

1.  Analyzing heat capacity profiles of peptide-containing membranes: cluster formation of gramicidin A.

Authors:  V P Ivanova; I M Makarov; T E Schäffer; T Heimburg
Journal:  Biophys J       Date:  2003-04       Impact factor: 4.033

2.  Detection of peptide-lipid interactions in mixed monolayers, using isotherms, atomic force microscopy, and fourier transform infrared analyses.

Authors:  V Vié; N Van Mau; L Chaloin; E Lesniewska; C Le Grimellec; F Heitz
Journal:  Biophys J       Date:  2000-02       Impact factor: 4.033

3.  Direct visualization of asymmetric behavior in supported lipid bilayers at the gel-fluid phase transition.

Authors:  Z Vivian Feng; Tighe A Spurlin; Andrew A Gewirth
Journal:  Biophys J       Date:  2004-12-13       Impact factor: 4.033

4.  Natively folded HypF-N and its early amyloid aggregates interact with phospholipid monolayers and destabilize supported phospholipid bilayers.

Authors:  Claudio Canale; Silvia Torrassa; Pasquale Rispoli; Annalisa Relini; Ranieri Rolandi; Monica Bucciantini; Massimo Stefani; Alessandra Gliozzi
Journal:  Biophys J       Date:  2006-09-22       Impact factor: 4.033

5.  Effect of gramicidin A on the dipole potential of phospholipid membranes.

Authors:  V L Shapovalov; E A Kotova; T I Rokitskaya; Y N Antonenko
Journal:  Biophys J       Date:  1999-07       Impact factor: 4.033

6.  Phase behavior and nanoscale structure of phospholipid membranes incorporated with acylated C14-peptides.

Authors:  Tina B Pedersen; Thomas Kaasgaard; Morten Ø Jensen; Sven Frokjaer; Ole G Mouritsen; Kent Jørgensen
Journal:  Biophys J       Date:  2005-08-12       Impact factor: 4.033

7.  Facile lipid flip-flop in a phospholipid bilayer induced by gramicidin A measured by sum-frequency vibrational spectroscopy.

Authors:  Timothy C Anglin; Jin Liu; John C Conboy
Journal:  Biophys J       Date:  2006-10-27       Impact factor: 4.033

8.  Spin-labeled gramicidin a: channel formation and dissociation.

Authors:  Boris G Dzikovski; Petr P Borbat; Jack H Freed
Journal:  Biophys J       Date:  2004-08-23       Impact factor: 4.033

9.  Membrane-mediated protein-protein interactions and connection to elastic models: a coarse-grained simulation analysis of gramicidin A association.

Authors:  Jejoong Yoo; Qiang Cui
Journal:  Biophys J       Date:  2013-01-08       Impact factor: 4.033

10.  Electron-spin resonance study of aggregation of gramicidin in dipalmitoylphosphatidylcholine bilayers and hydrophobic mismatch.

Authors:  M Ge; J H Freed
Journal:  Biophys J       Date:  1999-01       Impact factor: 4.033

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