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
到查詢結果
[ null ]
切換:
標籤
|
MARC模式
|
ISBD
Understanding T-Cell Receptor Signal...
~
White, William Louis,
FindBook
Google Book
Amazon
博客來
Understanding T-Cell Receptor Signaling Through Computational Modeling and De-novo Protein Design /
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Understanding T-Cell Receptor Signaling Through Computational Modeling and De-novo Protein Design // William Louis White.
作者:
White, William Louis,
面頁冊數:
1 electronic resource (67 pages)
附註:
Source: Dissertations Abstracts International, Volume: 86-01, Section: B.
Contained By:
Dissertations Abstracts International86-01B.
標題:
Bioengineering. -
電子資源:
https://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=31294680
ISBN:
9798383282915
Understanding T-Cell Receptor Signaling Through Computational Modeling and De-novo Protein Design /
White, William Louis,
Understanding T-Cell Receptor Signaling Through Computational Modeling and De-novo Protein Design /
William Louis White. - 1 electronic resource (67 pages)
Source: Dissertations Abstracts International, Volume: 86-01, Section: B.
In order to successfully defend the host from a wide range of pathogens and cancer, T-cells must be able to recognize these threats while ignoring healthy tissues. If T-cell threat recognition is not properly calibrated, pathologies such as autoimmunity or immune deficiency can arise. The mechanisms that control T-cell recognition and activation can be broadly divided into two categories: the structural mechanism by which T-cell receptors (TCRs) can bind specifically to foreign peptides presented on the major histocompatibility complex (pMHC) but not self-pMHCs, and the biochemical mechanism by which TCR binding events are translated into T-cell activation. Here, I describe two projects that are together focused on developing tools and models to better understand each of these critical aspects of T-cell function. First, I developed a de-novo designed stabilizing domain which allows MHCs to be expressed solubly in E. coli, allowing much faster and easier production of pMHC reagents for a variety of applications in the study of pMHC-TCR interactions. Second, I developed a model of early T-cell signaling steps which explains several important aspects of TCR signaling through the clustering dynamics of signaling molecules. In combination, these two projects provide important tools and insights in the study of T-cell antigen recognition and selectivity.
English
ISBN: 9798383282915Subjects--Topical Terms:
657580
Bioengineering.
Subjects--Index Terms:
Cell signaling
Understanding T-Cell Receptor Signaling Through Computational Modeling and De-novo Protein Design /
LDR
:03006nmm a22004933i 4500
001
2436487
005
20251023121225.5
006
m o d
007
cr|nu||||||||
008
261011s2024 miu||||||m |||||||eng d
020
$a
9798383282915
035
$a
(MiAaPQD)AAI31294680
035
$a
AAI31294680
040
$a
MiAaPQD
$b
eng
$c
MiAaPQD
$e
rda
100
1
$a
White, William Louis,
$e
author.
$3
3827144
245
1 0
$a
Understanding T-Cell Receptor Signaling Through Computational Modeling and De-novo Protein Design /
$c
William Louis White.
264
1
$a
Ann Arbor :
$b
ProQuest Dissertations & Theses,
$c
2024
300
$a
1 electronic resource (67 pages)
336
$a
text
$b
txt
$2
rdacontent
337
$a
computer
$b
c
$2
rdamedia
338
$a
online resource
$b
cr
$2
rdacarrier
500
$a
Source: Dissertations Abstracts International, Volume: 86-01, Section: B.
500
$a
Includes supplementary digital materials.
500
$a
Advisors: Baker, David; Kueh, Hao Yuan Committee members: Bradley, Philip H.; Maly, Dustin; Wiggins, Paul.
502
$b
Ph.D.
$c
University of Washington
$d
2024.
520
$a
In order to successfully defend the host from a wide range of pathogens and cancer, T-cells must be able to recognize these threats while ignoring healthy tissues. If T-cell threat recognition is not properly calibrated, pathologies such as autoimmunity or immune deficiency can arise. The mechanisms that control T-cell recognition and activation can be broadly divided into two categories: the structural mechanism by which T-cell receptors (TCRs) can bind specifically to foreign peptides presented on the major histocompatibility complex (pMHC) but not self-pMHCs, and the biochemical mechanism by which TCR binding events are translated into T-cell activation. Here, I describe two projects that are together focused on developing tools and models to better understand each of these critical aspects of T-cell function. First, I developed a de-novo designed stabilizing domain which allows MHCs to be expressed solubly in E. coli, allowing much faster and easier production of pMHC reagents for a variety of applications in the study of pMHC-TCR interactions. Second, I developed a model of early T-cell signaling steps which explains several important aspects of TCR signaling through the clustering dynamics of signaling molecules. In combination, these two projects provide important tools and insights in the study of T-cell antigen recognition and selectivity.
546
$a
English
590
$a
School code: 0250
650
4
$a
Bioengineering.
$3
657580
650
4
$a
Biochemistry.
$3
518028
650
4
$a
Immunology.
$3
611031
650
4
$a
Microbiology.
$3
536250
650
4
$a
Cellular biology.
$3
3172791
653
$a
Cell signaling
653
$a
Clustering
653
$a
MHC
653
$a
Protein design
653
$a
Soluble MHC
653
$a
T-cell receptor
690
$a
0202
690
$a
0487
690
$a
0982
690
$a
0379
690
$a
0410
710
2
$a
University of Washington.
$b
Bioengineering.
$e
degree granting institution.
$3
3827145
720
1
$a
Baker, David
$e
degree supervisor.
720
1
$a
Kueh, Hao Yuan
$e
degree supervisor.
773
0
$t
Dissertations Abstracts International
$g
86-01B.
790
$a
0250
791
$a
Ph.D.
792
$a
2024
856
4 0
$u
https://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=31294680
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
W9532182
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
(1)帳號:一般為「身分證號」;外籍生或交換生則為「學號」。 (2)密碼:預設為帳號末四碼。
帳號
.
密碼
.
請在此電腦上記得個人資料
取消
忘記密碼? (請注意!您必須已在系統登記E-mail信箱方能使用。)