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
Development of a synthetic peptide v...
~
Kao, Daniel Joseph.
FindBook
Google Book
Amazon
博客來
Development of a synthetic peptide vaccine and antibody therapeutic for the prevention and treatment of Pseudomonas aeruginosa infection.
紀錄類型:
書目-語言資料,印刷品 : Monograph/item
正題名/作者:
Development of a synthetic peptide vaccine and antibody therapeutic for the prevention and treatment of Pseudomonas aeruginosa infection./
作者:
Kao, Daniel Joseph.
面頁冊數:
261 p.
附註:
Adviser: Robert S. Hodges.
Contained By:
Dissertation Abstracts International68-08B.
標題:
Health Sciences, Immunology. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3277182
ISBN:
9780549190394
Development of a synthetic peptide vaccine and antibody therapeutic for the prevention and treatment of Pseudomonas aeruginosa infection.
Kao, Daniel Joseph.
Development of a synthetic peptide vaccine and antibody therapeutic for the prevention and treatment of Pseudomonas aeruginosa infection.
- 261 p.
Adviser: Robert S. Hodges.
Thesis (Ph.D.)--University of Colorado Health Sciences Center, 2007.
The type IV pilus is an adhesion that is critical in the pathogenesis of Pseudomonas aeruginosa infection and a good candidate for development of an anti-adhesin vaccine. The receptor binding domain of the type IV pilus resides in a C-terminal disulfide loop of the pilin subunit and is responsible for mediating adhesion to eukaryotic epithelia. In this study, a synthetic peptide vaccine targeting the receptor binding domain has been validated through analysis of polyclonal sera raised in mice and rabbits. We have shown that antibodies raised against the peptide immunogen domain are present in higher concentration and have higher affinity for the receptor binding domain of the intact pilin protein than antibodies raised against the pilin protein itself. We have also characterized a consensus sequence peptide immunogen, termed Cs1, which has been designed to generate an immune response that provides protection against infection by multiple strains of P. aeruginosa. We have shown that the Cs1 peptide can induce the production of antibodies that are cross-reactive against the PAK and PAO pilin proteins. The high resolution X-ray crystal structure of the Cs1 sequence in the context of an intact pilin protein was determined to gain insight into the structural basis for the novel immunological activity that was observed. There were few differences in the backbone conformation between the Cs1 structure and the known structures of native strain pilins. Based on these findings, we have proposed that the cross-reactivity of the immune response to Cs1 is modulated by the side chain composition of the solvent-exposed residues of the pilin receptor binding domain. Additionally, one of the consensus sequence substitutions may be important for stabilizing the secondary structure of the receptor binding domain, while the other substitution may be important for determining antibody specificity. In summary, we have demonstrated that a synthetic peptide vaccine targeting the type IV pilus of P. aeruginosa presents a number of advantages over using an intact pilin protein and have shown how modification of the peptide immunogen may modulate the antibody response to create a cross-protective vaccine.
ISBN: 9780549190394Subjects--Topical Terms:
1017716
Health Sciences, Immunology.
Development of a synthetic peptide vaccine and antibody therapeutic for the prevention and treatment of Pseudomonas aeruginosa infection.
LDR
:03186nam 2200277 a 45
001
938944
005
20110512
008
110512s2007 eng d
020
$a
9780549190394
035
$a
(UMI)AAI3277182
035
$a
AAI3277182
040
$a
UMI
$c
UMI
100
1
$a
Kao, Daniel Joseph.
$3
1262917
245
1 0
$a
Development of a synthetic peptide vaccine and antibody therapeutic for the prevention and treatment of Pseudomonas aeruginosa infection.
300
$a
261 p.
500
$a
Adviser: Robert S. Hodges.
500
$a
Source: Dissertation Abstracts International, Volume: 68-08, Section: B, page: 5159.
502
$a
Thesis (Ph.D.)--University of Colorado Health Sciences Center, 2007.
520
$a
The type IV pilus is an adhesion that is critical in the pathogenesis of Pseudomonas aeruginosa infection and a good candidate for development of an anti-adhesin vaccine. The receptor binding domain of the type IV pilus resides in a C-terminal disulfide loop of the pilin subunit and is responsible for mediating adhesion to eukaryotic epithelia. In this study, a synthetic peptide vaccine targeting the receptor binding domain has been validated through analysis of polyclonal sera raised in mice and rabbits. We have shown that antibodies raised against the peptide immunogen domain are present in higher concentration and have higher affinity for the receptor binding domain of the intact pilin protein than antibodies raised against the pilin protein itself. We have also characterized a consensus sequence peptide immunogen, termed Cs1, which has been designed to generate an immune response that provides protection against infection by multiple strains of P. aeruginosa. We have shown that the Cs1 peptide can induce the production of antibodies that are cross-reactive against the PAK and PAO pilin proteins. The high resolution X-ray crystal structure of the Cs1 sequence in the context of an intact pilin protein was determined to gain insight into the structural basis for the novel immunological activity that was observed. There were few differences in the backbone conformation between the Cs1 structure and the known structures of native strain pilins. Based on these findings, we have proposed that the cross-reactivity of the immune response to Cs1 is modulated by the side chain composition of the solvent-exposed residues of the pilin receptor binding domain. Additionally, one of the consensus sequence substitutions may be important for stabilizing the secondary structure of the receptor binding domain, while the other substitution may be important for determining antibody specificity. In summary, we have demonstrated that a synthetic peptide vaccine targeting the type IV pilus of P. aeruginosa presents a number of advantages over using an intact pilin protein and have shown how modification of the peptide immunogen may modulate the antibody response to create a cross-protective vaccine.
590
$a
School code: 0831.
650
4
$a
Health Sciences, Immunology.
$3
1017716
650
4
$a
Health Sciences, Pharmacology.
$3
1017717
690
$a
0419
690
$a
0982
710
2 0
$a
University of Colorado Health Sciences Center.
$3
1023815
773
0
$t
Dissertation Abstracts International
$g
68-08B.
790
$a
0831
790
1 0
$a
Hodges, Robert S.,
$e
advisor
791
$a
Ph.D.
792
$a
2007
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3277182
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
W9109132
電子資源
11.線上閱覽_V
電子書
EB W9109132
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