Structure, Assembly, and Maturation of High -Density Lipoproteins
Shih, Amy
This item is only available for download by members of the University of Illinois community. Students, faculty, and staff at the U of I may log in with your NetID and password to view the item. If you are trying to access an Illinois-restricted dissertation or thesis, you can request a copy through your library's Inter-Library Loan office or purchase a copy directly from ProQuest.
Permalink
https://hdl.handle.net/2142/87912
Description
Title
Structure, Assembly, and Maturation of High -Density Lipoproteins
Author(s)
Shih, Amy
Issue Date
2008
Doctoral Committee Chair(s)
Schulten, Klaus J.
Sligar, Stephen G.
Degree Granting Institution
University of Illinois at Urbana-Champaign
Degree Name
Ph.D.
Degree Level
Dissertation
Keyword(s)
Biophysics, General
Language
eng
Abstract
High-density lipoproteins (HDL) are protein-lipid particles that are involved in the transport of cholesterol in the blood. They are of great importance in the treatment of coronary heart disease as low levels of HDLs are a known risk factor for the development of arteriosclerosis. Little is known about the molecular level structure of these HDL particles or the mechanism by which they assemble from lipid-free proteins into discoidal protein-lipid particles and then into spherical particles. This thesis presents molecular dynamics simulations with comparisons to experimental small-angle X-ray scattering results which begin to characterize the initial stages of HDL biogenesis. Starting from all-atom simulations done to characterize the double-belt structure of discoidal HDL particles. Then moving on to the development and subsequent refinement of a coarse-grained protein-lipid model developed to allow for long timescale simulations of lipoproteins. The coarse-grained model is validated through comparisons with small-angle X-ray scattering measurements and by reverse coarse-graining methods. Self-assembly simulations of discoidal HDL particles were performed which showed the initial aggregation of proteins and lipids are driven by the hydrophobic effect. This is followed by a slower protein tertiary structure rearrangement which eventually results in the formation of a double-belt model discoidal HDL particle. The conversion of discoidal HDL into spherical HDL particles is investigated through the stepwise addition of cholesterol esters into an HDL particle using coarse-grained molecular dynamics. This process shows the dynamic formation of a hydrophobic cholesterol ester core which leads to change in the global particle shape. Reverse coarse-graining of the final spherical HDL particle, allows for the generation of a detailed atomic level image of a spherical HDL. Additionally, insights into how nanodiscs, a reconstituted discoidal HDL mimic, used as platforms for embedding and studying membrane proteins, are self-assembled or disassembled due to the presence of cholate molecules are presented.
Use this login method if you
don't
have an
@illinois.edu
email address.
(Oops, I do have one)
IDEALS migrated to a new platform on June 23, 2022. If you created
your account prior to this date, you will have to reset your password
using the forgot-password link below.
