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
The Role of Protein-Nucleic Acid Int...
~
East, Kyle William.
FindBook
Google Book
Amazon
博客來
The Role of Protein-Nucleic Acid Interactions in the Function and Fidelity of DNA Polymerase β and CRISPR Cas9 Monitored by NMR.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
The Role of Protein-Nucleic Acid Interactions in the Function and Fidelity of DNA Polymerase β and CRISPR Cas9 Monitored by NMR./
作者:
East, Kyle William.
出版者:
Ann Arbor : ProQuest Dissertations & Theses, : 2019,
面頁冊數:
148 p.
附註:
Source: Dissertations Abstracts International, Volume: 81-03, Section: B.
Contained By:
Dissertations Abstracts International81-03B.
標題:
Chemistry. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=13806441
ISBN:
9781085777407
The Role of Protein-Nucleic Acid Interactions in the Function and Fidelity of DNA Polymerase β and CRISPR Cas9 Monitored by NMR.
East, Kyle William.
The Role of Protein-Nucleic Acid Interactions in the Function and Fidelity of DNA Polymerase β and CRISPR Cas9 Monitored by NMR.
- Ann Arbor : ProQuest Dissertations & Theses, 2019 - 148 p.
Source: Dissertations Abstracts International, Volume: 81-03, Section: B.
Thesis (Ph.D.)--Yale University, 2019.
This item must not be sold to any third party vendors.
Protein-nucleic acid interactions are one of the most important processes required for life on earth. These interactions make up the core of the central dogma of molecular biology first published by Francis Crick in 1958. For over six decades, the interactions of proteins with DNA and RNA have been heavily studied in order to better understand how the proteome interacts with the genome and nucleic acid polymers. The complexity of these interactions is best highlighted by the thousands of proteins that interact with genomic DNA and various RNAs. These protein-nucleic acid interactions are required for the integrity of the genome and the stability of the processes required by the central dogma. The integrity of genomic DNA requires the fidelity of the DNA polymerases that copy and repair the millions of DNA base pairs per cell. One polymerase that repair DNA in humans is DNA polymerase β. Studies of DNA polymerase β (pol β) have shown that the interactions of pol β with the target DNA are tightly regulated to maximize the fidelity of the enzyme. The wild type enzyme was monitored using NMR spectroscopy in order to study the effects of the four template nucleotides (adenosine, guanosine, thymine, and cytosine) have on the structure and dynamics of the enzyme. The wild type enzyme was shown to bind independently of the nucleotide; however, the steric effects of the template nucleotide and the incoming nucleotide triphosphate show that the mechanism for selecting the appropriate nucleotide is heavily dependent on the steric effects of the base pair. To further these studies, several cancer-associated mutants of pol β have been identified that are still active polymerases but with reduced fidelity. One of these cancer-associated mutants, E288K, has a reduced fidelity only when the templating nucleotide is adenosine. This reduced fidelity allowed for the study of how the mutation of E288K altered the interaction of pol β with the target DNA.The CRISPR Cas9 endonuclease is an important molecular system for genome editing and the future of gene therapy. NMR studies of the entire Cas9 enzyme are hindered by the large size of the enzyme-RNA complex. Therefore, a construct of the HNH endonuclease domain of Cas9 was designed to allow for the assignment and study of part of Cas9. The HNH construct was assigned to 85%, allowing for the characterization of the internal structure and dynamics of the enzyme in solution by NMR. The HNH construct is structurally indistinguishable from the HNH domain of the full length Cas9 enzyme by x-ray crystallography. The measurement of dynamics on multiple time scales by NMR adds further evidence to the suggestion that the HNH domain is necessary for the communication between the PAM recognition domain and the second endonuclease domain, RuvC. This communication pathway is of great interest in the intelligent design of Cas9 enzymes for future gene therapy techniques.
ISBN: 9781085777407Subjects--Topical Terms:
516420
Chemistry.
Subjects--Index Terms:
Crispr-cas9
The Role of Protein-Nucleic Acid Interactions in the Function and Fidelity of DNA Polymerase β and CRISPR Cas9 Monitored by NMR.
LDR
:04132nmm a2200349 4500
001
2272383
005
20201105110042.5
008
220629s2019 ||||||||||||||||| ||eng d
020
$a
9781085777407
035
$a
(MiAaPQ)AAI13806441
035
$a
AAI13806441
040
$a
MiAaPQ
$c
MiAaPQ
100
1
$a
East, Kyle William.
$3
3549818
245
1 4
$a
The Role of Protein-Nucleic Acid Interactions in the Function and Fidelity of DNA Polymerase β and CRISPR Cas9 Monitored by NMR.
260
1
$a
Ann Arbor :
$b
ProQuest Dissertations & Theses,
$c
2019
300
$a
148 p.
500
$a
Source: Dissertations Abstracts International, Volume: 81-03, Section: B.
500
$a
Advisor: Loria, J. Patrick.
502
$a
Thesis (Ph.D.)--Yale University, 2019.
506
$a
This item must not be sold to any third party vendors.
506
$a
This item must not be added to any third party search indexes.
520
$a
Protein-nucleic acid interactions are one of the most important processes required for life on earth. These interactions make up the core of the central dogma of molecular biology first published by Francis Crick in 1958. For over six decades, the interactions of proteins with DNA and RNA have been heavily studied in order to better understand how the proteome interacts with the genome and nucleic acid polymers. The complexity of these interactions is best highlighted by the thousands of proteins that interact with genomic DNA and various RNAs. These protein-nucleic acid interactions are required for the integrity of the genome and the stability of the processes required by the central dogma. The integrity of genomic DNA requires the fidelity of the DNA polymerases that copy and repair the millions of DNA base pairs per cell. One polymerase that repair DNA in humans is DNA polymerase β. Studies of DNA polymerase β (pol β) have shown that the interactions of pol β with the target DNA are tightly regulated to maximize the fidelity of the enzyme. The wild type enzyme was monitored using NMR spectroscopy in order to study the effects of the four template nucleotides (adenosine, guanosine, thymine, and cytosine) have on the structure and dynamics of the enzyme. The wild type enzyme was shown to bind independently of the nucleotide; however, the steric effects of the template nucleotide and the incoming nucleotide triphosphate show that the mechanism for selecting the appropriate nucleotide is heavily dependent on the steric effects of the base pair. To further these studies, several cancer-associated mutants of pol β have been identified that are still active polymerases but with reduced fidelity. One of these cancer-associated mutants, E288K, has a reduced fidelity only when the templating nucleotide is adenosine. This reduced fidelity allowed for the study of how the mutation of E288K altered the interaction of pol β with the target DNA.The CRISPR Cas9 endonuclease is an important molecular system for genome editing and the future of gene therapy. NMR studies of the entire Cas9 enzyme are hindered by the large size of the enzyme-RNA complex. Therefore, a construct of the HNH endonuclease domain of Cas9 was designed to allow for the assignment and study of part of Cas9. The HNH construct was assigned to 85%, allowing for the characterization of the internal structure and dynamics of the enzyme in solution by NMR. The HNH construct is structurally indistinguishable from the HNH domain of the full length Cas9 enzyme by x-ray crystallography. The measurement of dynamics on multiple time scales by NMR adds further evidence to the suggestion that the HNH domain is necessary for the communication between the PAM recognition domain and the second endonuclease domain, RuvC. This communication pathway is of great interest in the intelligent design of Cas9 enzymes for future gene therapy techniques.
590
$a
School code: 0265.
650
4
$a
Chemistry.
$3
516420
650
4
$a
Biophysics.
$3
518360
653
$a
Crispr-cas9
653
$a
Dna polymerase beta
653
$a
Nmr
690
$a
0485
690
$a
0786
710
2
$a
Yale University.
$b
Chemistry.
$3
2101664
773
0
$t
Dissertations Abstracts International
$g
81-03B.
790
$a
0265
791
$a
Ph.D.
792
$a
2019
793
$a
English
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=13806441
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
W9424617
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