語系:
繁體中文
English
說明(常見問題)
回圖書館首頁
手機版館藏查詢
登入
回首頁
切換:
標籤
|
MARC模式
|
ISBD
Retroviral capsid assembly.
~
Ganser, Barbie Kay.
FindBook
Google Book
Amazon
博客來
Retroviral capsid assembly.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Retroviral capsid assembly./
作者:
Ganser, Barbie Kay.
面頁冊數:
149 p.
附註:
Source: Dissertation Abstracts International, Volume: 63-12, Section: B, page: 5821.
Contained By:
Dissertation Abstracts International63-12B.
標題:
Chemistry, Biochemistry. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3074057
ISBN:
0493941029
Retroviral capsid assembly.
Ganser, Barbie Kay.
Retroviral capsid assembly.
- 149 p.
Source: Dissertation Abstracts International, Volume: 63-12, Section: B, page: 5821.
Thesis (Ph.D.)--The University of Utah, 2003.
During retroviral maturation, the viral CA protein oligomerizes to form a closed capsid that surrounds the viral genome. Interestingly, mature capsid morphologies vary dramatically across the different genera of retroviridae. Specifically, capsids can be conical, spherical, or cylindrical. Despite these morphological differences, however, the tertiary structure of CA proteins is conserved across all genera, suggesting that there may be commonalities in the structure of all capsids. This dissertation reports biochemical and structural studies of retroviral CA assemblies formed in vitro, with the goal of understanding the structure and conservation of retroviral capsids.
ISBN: 0493941029Subjects--Topical Terms:
1017722
Chemistry, Biochemistry.
Retroviral capsid assembly.
LDR
:03328nmm 2200325 4500
001
1855157
005
20040624070200.5
008
130614s2003 eng d
020
$a
0493941029
035
$a
(UnM)AAI3074057
035
$a
AAI3074057
040
$a
UnM
$c
UnM
100
1
$a
Ganser, Barbie Kay.
$3
1942977
245
1 0
$a
Retroviral capsid assembly.
300
$a
149 p.
500
$a
Source: Dissertation Abstracts International, Volume: 63-12, Section: B, page: 5821.
500
$a
Adviser: Wesley Ian Sundquist.
502
$a
Thesis (Ph.D.)--The University of Utah, 2003.
520
$a
During retroviral maturation, the viral CA protein oligomerizes to form a closed capsid that surrounds the viral genome. Interestingly, mature capsid morphologies vary dramatically across the different genera of retroviridae. Specifically, capsids can be conical, spherical, or cylindrical. Despite these morphological differences, however, the tertiary structure of CA proteins is conserved across all genera, suggesting that there may be commonalities in the structure of all capsids. This dissertation reports biochemical and structural studies of retroviral CA assemblies formed in vitro, with the goal of understanding the structure and conservation of retroviral capsids.
520
$a
Helical assemblies made from HIV-1 CA are composed of hexamers. This work led us to propose that the conical HIV-1 capsid could be built on a hexameric lattice closed by asymmetrically introducing twelve pentameric defects. A corollary of our model is that within these conical assemblies, only five cone angles are allowed. Therefore, we developed a method for producing HIV-1 CA conical assemblies in vitro, and measurements of ∼1,000 of these synthetic cones revealed that the predicted angles are preferentially populated.
520
$a
High-resolution studies of the HIV-1 CA protein have been combined with helical reconstructions of HIV-1 CA to create a pseudoatomic model of the viral capsid. CA interfaces present in the model are predicted to be important for HIV-1 assembly. Indeed, alanine scanning mutagenesis demonstrated that these interfaces are important for CA cylinder assembly in vitro. Interestingly, this study also revealed a CA mutant (R18A), which could assemble into spheres, cylinders and cones (the three capsid morphologies seen within authentic virions).
520
$a
Finally, we have proposed that all retroviral capsids are composed of hexameric arrays of CA protein similar to those defined for HIV-1, and that the distinct morphologies of retroviral capsids reflect different distributions of the pentameric declinations that allow the structures to close. Therefore, we determined the three dimensional structure of MMuLV CA crystallized on a lipid monolayer and found that M-MuLV also assembles into hexamers similar to those reported for HIV-1.
520
$a
In summary, this dissertation proposes a general model for retroviral assembly, wherein all retroviral capsids are built on similar hexameric lattices closed by pentameric defects.
590
$a
School code: 0240.
650
4
$a
Chemistry, Biochemistry.
$3
1017722
650
4
$a
Biology, Microbiology.
$3
1017734
690
$a
0487
690
$a
0410
710
2 0
$a
The University of Utah.
$3
1017410
773
0
$t
Dissertation Abstracts International
$g
63-12B.
790
1 0
$a
Sundquist, Wesley Ian,
$e
advisor
790
$a
0240
791
$a
Ph.D.
792
$a
2003
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3074057
筆 0 讀者評論
館藏地:
全部
電子資源
出版年:
卷號:
館藏
1 筆 • 頁數 1 •
1
條碼號
典藏地名稱
館藏流通類別
資料類型
索書號
使用類型
借閱狀態
預約狀態
備註欄
附件
W9173857
電子資源
11.線上閱覽_V
電子書
EB
一般使用(Normal)
在架
0
1 筆 • 頁數 1 •
1
多媒體
評論
新增評論
分享你的心得
Export
取書館
處理中
...
變更密碼
登入