Structure and Physicochemical Properties of Phospholipidic Monolayers and Bilayers. LB and AFM Studies

[eng] The main objective of this Ph. D. Thesis work was to study the physicochemical properties of the inner membrane of mitochondria and the interaction of "cyt c" with model membranes. Suitable techniques were used to accomplish this objective: Langmuir and Langmuir Blodgett films, fluor...

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Detalles Bibliográficos
Autor: Domènech Cabrera, Òscar
Tipo de recurso: tesis doctoral
Estado:Versión publicada
Fecha de publicación:2007
País:España
Institución:Universidad de Barcelona
Repositorio:Dipòsit Digital de la UB
OAI Identifier:oai:diposit.ub.edu:2445/42866
Acceso en línea:https://hdl.handle.net/2445/42866
http://www.tdx.cat/TDX-0912108-120530
http://hdl.handle.net/10803/2758
Access Level:acceso abierto
Palabra clave:Membranes (Biologia)
Micel·les
Membranes cel·lulars
Lípids
Biosíntesi
Membranes (Biology)
Micelles
Cell membranes
Lipids
Biosynthesis
Descripción
Sumario:[eng] The main objective of this Ph. D. Thesis work was to study the physicochemical properties of the inner membrane of mitochondria and the interaction of "cyt c" with model membranes. Suitable techniques were used to accomplish this objective: Langmuir and Langmuir Blodgett films, fluorescence spectroscopy, Brewster Angle Microscopy and Atomic Force Microscopy. The general conclusion of this Thesis is: "Calcium induces HII phases in POPE:CL (0.8:0.2, mol:mol) samples in solution. This composition is the most stable mixed monolayer of both phospholipids and corresponds to the native molar fraction in the inner membrane of the mitochondrion. The extension of these inverted micelles forms planar bilayers on solid supports displaying lateral lipid segregation of CL enriched domains where cyt "c can" bind specifically. In this configuration POPC can remain as a spacer in POPE enriched domains forming the matrix of the membrane". The inverse process would be a possible vindication to the release of "cyt c" from the inner membrane of mitochondrion during apoptosis.