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root/group/trunk/tengDissertation/Lipid.tex
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# Content
1 \chapter{\label{chapt:lipid}LIPID MODELING}
2
3 \section{\label{lipidSection:introduction}Introduction}
4
5 Under biologically relevant conditions, phospholipids are solvated
6 in aqueous solutions at a roughly 25:1 ratio. Solvation can have a
7 tremendous impact on transport phenomena in biological membranes
8 since it can affect the dynamics of ions and molecules that are
9 transferred across membranes. Studies suggest that because of the
10 directional hydrogen bonding ability of the lipid headgroups, a
11 small number of water molecules are strongly held around the
12 different parts of the headgroup and are oriented by them with
13 residence times for the first hydration shell being around 0.5 - 1
14 ns.[14] In the second solvation shell, some water molecules are
15 weakly bound, but are still essential for determining the properties
16 of the system. Transport of various molecular species into living
17 cells is one of the major functions of membranes. A thorough
18 understanding of the underlying molecular mechanism for solute
19 diffusion is crucial to the further studies of other related
20 biological processes. All transport across cell membranes takes
21 place by one of two fundamental processes: Passive transport is
22 driven by bulk or inter-diffusion of the molecules being transported
23 or by membrane pores which facilitate crossing. Active transport
24 depends upon the expenditure of cellular energy in the form of ATP
25 hydrolysis. As the central processes of membrane assembly,
26 translocation of phospholipids across membrane bilayers requires the
27 hydrophilic head of the phospholipid to pass through the highly
28 hydrophobic interior of the membrane, and for the hydrophobic tails
29 to be exposed to the aqueous environment.[18] A number of studies
30 indicate that the flipping of phospholipids occurs rapidly in the
31 eukaryotic ER and the bacterial cytoplasmic membrane via a
32 bi-directional, facilitated diffusion process requiring no metabolic
33 energy input. Another system of interest would be the distribution
34 of sites occupied by inhaled anesthetics in membrane. Although the
35 physiological effects of anesthetics have been extensively studied,
36 the controversy over their effects on lipid bilayers still
37 continues. Recent deuterium NMR measurements on halothane in POPC
38 lipid bilayers suggest the anesthetics are primarily located at the
39 hydrocarbon chain region.[16] Infrared spectroscopy experiments
40 suggest that halothane in DMPC lipid bilayers lives near the
41 membrane/water interface. [17]
42
43
44 \section{\label{lipidSection:model}Model}
45
46 \section{\label{lipidSection:methods}Methods}
47
48 \section{\label{lipidSection:resultDiscussion}Results and Discussion}