Studies of cholesterol structures in phospholipid bilayers

Experiments and Monte Carlo (MC) simulations on ergosterol/nystatin channels providestrong evidence for superlattices in ergosterol/phospholipid planar bilayers. Monte Carlo simulationsalso revealed the presence of ergosterol superlattice domains in artificial vesicle membranes. MC simulation for er...

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Main Author: Carl S. Helrich
Format: Article
Language:English
Published: AIMS Press 2017-06-01
Series:AIMS Biophysics
Subjects:
Online Access:http://www.aimspress.com/biophysics/article/1485/fulltext.html
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spelling doaj-b15f30094fa54182b71da204f4029d362020-11-25T01:52:32ZengAIMS PressAIMS Biophysics2377-90982017-06-014341543710.3934/biophy.2017.3.415biophys-04-00415Studies of cholesterol structures in phospholipid bilayersCarl S. Helrich0Department of Physics, Goshen College, Goshen, Indiana, USAExperiments and Monte Carlo (MC) simulations on ergosterol/nystatin channels providestrong evidence for superlattices in ergosterol/phospholipid planar bilayers. Monte Carlo simulationsalso revealed the presence of ergosterol superlattice domains in artificial vesicle membranes. MC simulation for ergosterol densities in these domains matched the dehydroergosterol (DHE) fluorescence measurements by Chong of dehydroergosterol density in multilamellar vesicles. Withergosterol/nystatin channels on the boundaries of these domains MC simulations produced agreement with experimental measurements of ergosterol/nystatin channel currents. These techniques, however, failed for cholesterol/nystatin channels. Although studies of initial dynamics in the formation ofergosterol/nystatin channels confirm ergosterol superlattices, they fail for cholesterol/nystatin channels. However a Fast Fourier Transform based study of the frequency of fluctuation spikes present inlow density cholesterol/nystatin channel currents revealed a dependence of spike frequency oncholesterol mol fraction which matched cholesterol density from DHE/cholesterol/DMPC fluorescence experiments. This indicates the probable presence of superlattices in cholesterol structures in phospholipid bilayers. The causal relationship between these statistical channel fluctuations andcholesterol structure is notable in its own right.http://www.aimspress.com/biophysics/article/1485/fulltext.htmlergosterolcholesterolnystatinphospholipidbilayervesiclessuperlattice
collection DOAJ
language English
format Article
sources DOAJ
author Carl S. Helrich
spellingShingle Carl S. Helrich
Studies of cholesterol structures in phospholipid bilayers
AIMS Biophysics
ergosterol
cholesterol
nystatin
phospholipid
bilayer
vesicles
superlattice
author_facet Carl S. Helrich
author_sort Carl S. Helrich
title Studies of cholesterol structures in phospholipid bilayers
title_short Studies of cholesterol structures in phospholipid bilayers
title_full Studies of cholesterol structures in phospholipid bilayers
title_fullStr Studies of cholesterol structures in phospholipid bilayers
title_full_unstemmed Studies of cholesterol structures in phospholipid bilayers
title_sort studies of cholesterol structures in phospholipid bilayers
publisher AIMS Press
series AIMS Biophysics
issn 2377-9098
publishDate 2017-06-01
description Experiments and Monte Carlo (MC) simulations on ergosterol/nystatin channels providestrong evidence for superlattices in ergosterol/phospholipid planar bilayers. Monte Carlo simulationsalso revealed the presence of ergosterol superlattice domains in artificial vesicle membranes. MC simulation for ergosterol densities in these domains matched the dehydroergosterol (DHE) fluorescence measurements by Chong of dehydroergosterol density in multilamellar vesicles. Withergosterol/nystatin channels on the boundaries of these domains MC simulations produced agreement with experimental measurements of ergosterol/nystatin channel currents. These techniques, however, failed for cholesterol/nystatin channels. Although studies of initial dynamics in the formation ofergosterol/nystatin channels confirm ergosterol superlattices, they fail for cholesterol/nystatin channels. However a Fast Fourier Transform based study of the frequency of fluctuation spikes present inlow density cholesterol/nystatin channel currents revealed a dependence of spike frequency oncholesterol mol fraction which matched cholesterol density from DHE/cholesterol/DMPC fluorescence experiments. This indicates the probable presence of superlattices in cholesterol structures in phospholipid bilayers. The causal relationship between these statistical channel fluctuations andcholesterol structure is notable in its own right.
topic ergosterol
cholesterol
nystatin
phospholipid
bilayer
vesicles
superlattice
url http://www.aimspress.com/biophysics/article/1485/fulltext.html
work_keys_str_mv AT carlshelrich studiesofcholesterolstructuresinphospholipidbilayers
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