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Lateral heterogeneities in supported bilayers from pure and mixed phosphatidylethanolamine demonstrating hydrogen bonding capacity
Author(s) -
Matthew R. Nussio,
Nicolas H. Voelcker,
Matthew J. Sykes,
Steven J. P. McInnes,
Christopher T. Gibson,
Rachel D. Lowe,
John O. Miners,
Joseph G. Shapter
Publication year - 2008
Publication title -
biointerphases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.633
H-Index - 45
eISSN - 1934-8630
pISSN - 1559-4106
DOI - 10.1116/1.3040158
Subject(s) - hydrogen bond , chemistry , phosphatidylethanolamine , chemical physics , bilayer , crystallography , chemical engineering , nanotechnology , membrane , phospholipid , materials science , molecule , organic chemistry , phosphatidylcholine , engineering , biochemistry
The phase behavior and lateral organization of saturated phosphatidylethanolamine (PE) and phosphatidylcholine (PC) bilayers were investigated using atomic force microscopy (AFM) and force-volume (FV) imaging for both pure and two component mixed layers. The results demonstrated the existence of unexpected segregated domains in pure PE membranes at temperatures well below the transition temperature (T(m)) of the component phospholipid. These domains were of low mechanical stability and lacked the capacity for hydrogen bonding between lipid headgroups. Temperature dependent studies for different PC/PE ratios using AFM also demonstrated the mixing of these phospholipid bilayers to exhibit only a single gel to liquid transition temperature. Further work performed using FV imaging and chemically modified probes established that no lipid segregation exists at the PC/PE ratios investigated.

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