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
Single cell characterization of bioc...
~
Vogel, Robert Michael.
FindBook
Google Book
Amazon
博客來
Single cell characterization of biochemical noise and variable response to chemical inhibition.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Single cell characterization of biochemical noise and variable response to chemical inhibition./
作者:
Vogel, Robert Michael.
出版者:
Ann Arbor : ProQuest Dissertations & Theses, : 2016,
面頁冊數:
132 p.
附註:
Source: Dissertation Abstracts International, Volume: 77-06(E), Section: B.
Contained By:
Dissertation Abstracts International77-06B(E).
標題:
Biophysics. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10007588
ISBN:
9781339449081
Single cell characterization of biochemical noise and variable response to chemical inhibition.
Vogel, Robert Michael.
Single cell characterization of biochemical noise and variable response to chemical inhibition.
- Ann Arbor : ProQuest Dissertations & Theses, 2016 - 132 p.
Source: Dissertation Abstracts International, Volume: 77-06(E), Section: B.
Thesis (Ph.D.)--Weill Medical College of Cornell University, 2016.
Individual cells utilize series of biochemical reactions, called signaling pathways, to translate environmental conditions to physiological responses. Consequently, the emergent properties of these signaling pathways are constrained to the physico-chemical laws of their biochemical constituents - they are strongly dependent on the number of molecular components per cell, intrinsically stochastic (noisy), and are inherently nonlinear. While these properties provide the plasticity required for a functioning living system, they present challenges for our understanding and control of cellular behavior. In this thesis I present single cell measurements (i.e. flow cytometry data) and physical models that we developed to track fluctuations in protein and phospho-protein abundance throughout biochemical reaction networks, and demonstrate how the nonlinear properties of biochemical reactions produce unique network responses to the targeted chemical inhibition of enzymes. We track the logarithmic fluctuations of biochemical components using a system of chemical Langevin equations and the corresponding Lyapunov equation. Used together, these equations uncover the connection between the organization of signaling pathway constituents and the covariance matrix estimated from the experimental data. With this formalism we theoretically explore the unique covariance representations of various signaling pathways, and experimentally validate our method in two established systems: a synthetic E. coli gene regulatory network and the Mitogen Activated Protein Kinase (MAPK) cascade in primary mouse T lymphocytes. In addition, we use single cell measurements to mechanistically uncover the unique responses of signaling pathways, analog or digital, to targeted chemical inhibition. We extend these short time-scale properties of signaling pathways to a functional response, proliferation. Lastly, we show how the endogenous diversity of protein abundance among single cell clones provides a mechanism of resilience to chemical inhibition. Together, our combined experimental and theoretical approach provides novel insights to cellular systems, a method for directional inference, and optimal drug selection.
ISBN: 9781339449081Subjects--Topical Terms:
518360
Biophysics.
Single cell characterization of biochemical noise and variable response to chemical inhibition.
LDR
:03199nmm a2200301 4500
001
2119526
005
20170628084153.5
008
180830s2016 ||||||||||||||||| ||eng d
020
$a
9781339449081
035
$a
(MiAaPQ)AAI10007588
035
$a
AAI10007588
040
$a
MiAaPQ
$c
MiAaPQ
100
1
$a
Vogel, Robert Michael.
$3
3281402
245
1 0
$a
Single cell characterization of biochemical noise and variable response to chemical inhibition.
260
1
$a
Ann Arbor :
$b
ProQuest Dissertations & Theses,
$c
2016
300
$a
132 p.
500
$a
Source: Dissertation Abstracts International, Volume: 77-06(E), Section: B.
500
$a
Adviser: Gregoire Altan-Bonnet.
502
$a
Thesis (Ph.D.)--Weill Medical College of Cornell University, 2016.
520
$a
Individual cells utilize series of biochemical reactions, called signaling pathways, to translate environmental conditions to physiological responses. Consequently, the emergent properties of these signaling pathways are constrained to the physico-chemical laws of their biochemical constituents - they are strongly dependent on the number of molecular components per cell, intrinsically stochastic (noisy), and are inherently nonlinear. While these properties provide the plasticity required for a functioning living system, they present challenges for our understanding and control of cellular behavior. In this thesis I present single cell measurements (i.e. flow cytometry data) and physical models that we developed to track fluctuations in protein and phospho-protein abundance throughout biochemical reaction networks, and demonstrate how the nonlinear properties of biochemical reactions produce unique network responses to the targeted chemical inhibition of enzymes. We track the logarithmic fluctuations of biochemical components using a system of chemical Langevin equations and the corresponding Lyapunov equation. Used together, these equations uncover the connection between the organization of signaling pathway constituents and the covariance matrix estimated from the experimental data. With this formalism we theoretically explore the unique covariance representations of various signaling pathways, and experimentally validate our method in two established systems: a synthetic E. coli gene regulatory network and the Mitogen Activated Protein Kinase (MAPK) cascade in primary mouse T lymphocytes. In addition, we use single cell measurements to mechanistically uncover the unique responses of signaling pathways, analog or digital, to targeted chemical inhibition. We extend these short time-scale properties of signaling pathways to a functional response, proliferation. Lastly, we show how the endogenous diversity of protein abundance among single cell clones provides a mechanism of resilience to chemical inhibition. Together, our combined experimental and theoretical approach provides novel insights to cellular systems, a method for directional inference, and optimal drug selection.
590
$a
School code: 0967.
650
4
$a
Biophysics.
$3
518360
650
4
$a
Biochemistry.
$3
518028
650
4
$a
Genetics.
$3
530508
690
$a
0786
690
$a
0487
690
$a
0369
710
2
$a
Weill Medical College of Cornell University.
$b
Physiology, Biophysics and Systems Biology.
$3
3281403
773
0
$t
Dissertation Abstracts International
$g
77-06B(E).
790
$a
0967
791
$a
Ph.D.
792
$a
2016
793
$a
English
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10007588
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
W9330144
電子資源
01.外借(書)_YB
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