Language:
English
繁體中文
Help
回圖書館首頁
手機版館藏查詢
Login
Back
Switch To:
Labeled
|
MARC Mode
|
ISBD
Structure, ordering, and activity of...
~
The University of Chicago.
Linked to FindBook
Google Book
Amazon
博客來
Structure, ordering, and activity of lipid/polymer systems.
Record Type:
Language materials, printed : Monograph/item
Title/Author:
Structure, ordering, and activity of lipid/polymer systems./
Author:
Frey, Shelli Lynne.
Description:
373 p.
Notes:
Adviser: Ka Yee C. Lee.
Contained By:
Dissertation Abstracts International69-07B.
Subject:
Chemistry, Physical. -
Online resource:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3322585
ISBN:
9780549740292
Structure, ordering, and activity of lipid/polymer systems.
Frey, Shelli Lynne.
Structure, ordering, and activity of lipid/polymer systems.
- 373 p.
Adviser: Ka Yee C. Lee.
Thesis (Ph.D.)--The University of Chicago, 2008.
Lipid-lipid, lipid-polymer, lipid-peptide interactions in model cell membranes were characterized to pinpoint how variations in molecular architecture affect subsequent ordering, inducement of structures, and activity of these different mixtures. Lipid monolayers, at the air/water interface and also deposited on solid supports, served as models for the cell membrane outer leaflet and were probed with surface pressure versus area isotherms, fluorescence microscopy, atomic force microscopy, and also X-ray scattering techniques.
ISBN: 9780549740292Subjects--Topical Terms:
560527
Chemistry, Physical.
Structure, ordering, and activity of lipid/polymer systems.
LDR
:03503nam 2200325 a 45
001
861226
005
20100719
008
100719s2008 ||||||||||||||||| ||eng d
020
$a
9780549740292
035
$a
(UMI)AAI3322585
035
$a
AAI3322585
040
$a
UMI
$c
UMI
100
1
$a
Frey, Shelli Lynne.
$3
1028900
245
1 0
$a
Structure, ordering, and activity of lipid/polymer systems.
300
$a
373 p.
500
$a
Adviser: Ka Yee C. Lee.
500
$a
Source: Dissertation Abstracts International, Volume: 69-07, Section: B, page: 4190.
502
$a
Thesis (Ph.D.)--The University of Chicago, 2008.
520
$a
Lipid-lipid, lipid-polymer, lipid-peptide interactions in model cell membranes were characterized to pinpoint how variations in molecular architecture affect subsequent ordering, inducement of structures, and activity of these different mixtures. Lipid monolayers, at the air/water interface and also deposited on solid supports, served as models for the cell membrane outer leaflet and were probed with surface pressure versus area isotherms, fluorescence microscopy, atomic force microscopy, and also X-ray scattering techniques.
520
$a
Interactions of triblock copolymers, known to be healing agents for electroporated cells, with lipid monolayers were characterized with conventional lipid monolayer methods and Monte Carlo simulations. Factors such as temperature, size of polymer blocks, and the hydrophilic:hydrophobic ratio affect polymer solubility in both the subphase and the membrane suggesting a degree of tunability for biomedical applications involving polymer incorporation into lipid membranes.
520
$a
A subset of glycolipids, gangliosides, known to partition into lipid rafts, or ordered portions of the cell membrane, were shown to influence the phase behavior of neighboring lipids, causing a condensation of the layer at low mol% followed by fluidization with further addition of ganglioside. This effect is attributed to the wedge-shaped geometry of the ganglioside headgroup that forms a geometric close-packed complex with the surrounding phospholipid. The structure of gangliosides and induced organization in both monolayers and vesicles mediate amyloid beta fibril formation and subsequent membrane disruption implicated in Alzheimer's disease.
520
$a
Using different ratios of components in the binary lipid/ganglioside system to create membranes with systematically varying material properties, we show that membrane fluidity affects the monolayer reaction to lateral compression; a general criterion has been developed dictating whether a lipid monolayer folds into the third dimension at high surface compressions.
520
$a
The molecular architecture and flexibility of lung surfactant truncation peptide B affects its activity in model pulmonary surfactant with the N-terminal insertion sequence essential to support formation of three-dimensional reversible repositories of collapsed materials necessary for proper lung function at high surface pressures. Structure was also implicated in monolayer ordering when compressed binary mixtures of lipid and polymer at specific mole ratios are expanded though a labyrinthine transition that occurs at vanishing surface pressure.
590
$a
School code: 0330.
650
4
$a
Chemistry, Physical.
$3
560527
650
4
$a
Chemistry, Polymer.
$3
1018428
690
$a
0494
690
$a
0495
710
2
$a
The University of Chicago.
$3
1017389
773
0
$t
Dissertation Abstracts International
$g
69-07B.
790
$a
0330
790
1 0
$a
Lee, Ka Yee C.,
$e
advisor
791
$a
Ph.D.
792
$a
2008
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3322585
based on 0 review(s)
Location:
ALL
電子資源
Year:
Volume Number:
Items
1 records • Pages 1 •
1
Inventory Number
Location Name
Item Class
Material type
Call number
Usage Class
Loan Status
No. of reservations
Opac note
Attachments
W9074848
電子資源
11.線上閱覽_V
電子書
EB W9074848
一般使用(Normal)
On shelf
0
1 records • Pages 1 •
1
Multimedia
Reviews
Add a review
and share your thoughts with other readers
Export
pickup library
Processing
...
Change password
Login