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Revision 2730 by tim, Mon Apr 3 18:07:54 2006 UTC vs.
Revision 2731 by tim, Mon Apr 24 18:50:41 2006 UTC

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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}

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