語系:
繁體中文
English
說明(常見問題)
圖資館首頁
登入
回首頁
切換:
標籤
|
MARC模式
|
ISBD
Design and construction of novel DNA...
~
Keum, Jung Won.
Design and construction of novel DNA nanostructures for therapeutic applications.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Design and construction of novel DNA nanostructures for therapeutic applications.
作者:
Keum, Jung Won.
面頁冊數:
102 p.
附註:
Source: Dissertation Abstracts International, Volume: 73-12(E), Section: B.
附註:
Adviser: Harry Bermudez.
Contained By:
Dissertation Abstracts International73-12B(E).
標題:
Engineering, Biomedical.
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3518249
ISBN:
9781267493668
Design and construction of novel DNA nanostructures for therapeutic applications.
Keum, Jung Won.
Design and construction of novel DNA nanostructures for therapeutic applications.
- 102 p.
Source: Dissertation Abstracts International, Volume: 73-12(E), Section: B.
Thesis (Ph.D.)--University of Massachusetts Amherst, 2012.
Beyond the biological applications, the unique molecular recognition properties of DNA are of interest as ideal building blocks. Rationally designed DNA nanostructures serve as excellent delivery vehicles due to their well-defined three dimensional nanostructures and versatile conjugations with biomolecules. Additionally, nucleic acid motifs can have numerous functions through the mechanisms of riboswitches, DNAzymes, I-motif, aptamers, and antisense or RNA interference. The combination of both structural and functional aspects of DNA properties enables generation of versatile nano-materials that can interact with biological molecules and trigger specific responses to its environment. We previously reported the enhanced stability of a DNA tetrahedron to both specific and non-specific enzymatic digestion. The enhanced stability of DNA nanostructures motivated us to construct DNA pyramids with antisense capabilities. We have demonstrated the construction of DNA pyramids that are capable of delivering antisense DNA, thereby degrading mRNA and subsequently inhibiting target protein expression in vitro. We were able to confirm antisense activity of the DNA pyramids by the down-regulation of both EGFP and a tumor related protein MDM2 in mammalian cells. To explore additional responsive character of DNA nanostructures, we introduced an I-motif, which is formed under acidic condition, to the DNA nanostructures so that a DNA pyramid is able to exhibit pH responsive features. A pH change triggers a conformational change of the DNA pyramid, thereby enabling release of a cargo inside the DNA pyramid. Circular dichroism and FRET analysis were used to confirm the pH dependent formation of an I-motif and subsequent changes in DNA pyramid size. Dissociation of a cargo protein EGFP from the DNA pyramid was achieved using either pH, addition of EDTA or imidazole. We believe that by integrating multi-functional groups in DNA nanostructures and exploring responsive character of DNA nanostructures, powerful and versatile nano-biomaterials will be generated.
ISBN: 9781267493668Subjects--Topical Terms:
227004
Engineering, Biomedical.
Design and construction of novel DNA nanostructures for therapeutic applications.
LDR
:03158nmm 2200325 4500
001
380672
005
20130530092724.5
008
130708s2012 ||||||||||||||||| ||eng d
020
$a
9781267493668
035
$a
(UMI)AAI3518249
035
$a
AAI3518249
040
$a
UMI
$c
UMI
100
1
$a
Keum, Jung Won.
$3
603276
245
1 0
$a
Design and construction of novel DNA nanostructures for therapeutic applications.
300
$a
102 p.
500
$a
Source: Dissertation Abstracts International, Volume: 73-12(E), Section: B.
500
$a
Adviser: Harry Bermudez.
502
$a
Thesis (Ph.D.)--University of Massachusetts Amherst, 2012.
520
$a
Beyond the biological applications, the unique molecular recognition properties of DNA are of interest as ideal building blocks. Rationally designed DNA nanostructures serve as excellent delivery vehicles due to their well-defined three dimensional nanostructures and versatile conjugations with biomolecules. Additionally, nucleic acid motifs can have numerous functions through the mechanisms of riboswitches, DNAzymes, I-motif, aptamers, and antisense or RNA interference. The combination of both structural and functional aspects of DNA properties enables generation of versatile nano-materials that can interact with biological molecules and trigger specific responses to its environment. We previously reported the enhanced stability of a DNA tetrahedron to both specific and non-specific enzymatic digestion. The enhanced stability of DNA nanostructures motivated us to construct DNA pyramids with antisense capabilities. We have demonstrated the construction of DNA pyramids that are capable of delivering antisense DNA, thereby degrading mRNA and subsequently inhibiting target protein expression in vitro. We were able to confirm antisense activity of the DNA pyramids by the down-regulation of both EGFP and a tumor related protein MDM2 in mammalian cells. To explore additional responsive character of DNA nanostructures, we introduced an I-motif, which is formed under acidic condition, to the DNA nanostructures so that a DNA pyramid is able to exhibit pH responsive features. A pH change triggers a conformational change of the DNA pyramid, thereby enabling release of a cargo inside the DNA pyramid. Circular dichroism and FRET analysis were used to confirm the pH dependent formation of an I-motif and subsequent changes in DNA pyramid size. Dissociation of a cargo protein EGFP from the DNA pyramid was achieved using either pH, addition of EDTA or imidazole. We believe that by integrating multi-functional groups in DNA nanostructures and exploring responsive character of DNA nanostructures, powerful and versatile nano-biomaterials will be generated.
590
$a
School code: 0118.
650
4
$a
Engineering, Biomedical.
$3
227004
650
4
$a
Engineering, Chemical.
$3
226989
650
4
$a
Health Sciences, Pharmacy.
$3
226994
690
$a
0541
690
$a
0542
690
$a
0572
710
2
$a
University of Massachusetts Amherst.
$b
Chemical Engineering.
$3
603277
773
0
$t
Dissertation Abstracts International
$g
73-12B(E).
790
1 0
$a
Bermudez, Harry,
$e
advisor
790
1 0
$a
Mountziaris, T.J. (Lakis)
$e
committee member
790
1 0
$a
Forbes, Neil S.
$e
committee member
790
1 0
$a
Thayumanavan, Sankaran
$e
committee member
790
$a
0118
791
$a
Ph.D.
792
$a
2012
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3518249
筆 0 讀者評論
全部
電子館藏
館藏
1 筆 • 頁數 1 •
1
條碼號
館藏地
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
000000079209
電子館藏
1圖書
學位論文
TH 2012
一般使用(Normal)
在架
0
1 筆 • 頁數 1 •
1
多媒體
多媒體檔案
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3518249
評論
新增評論
分享你的心得
Export
取書館別
處理中
...
變更密碼
登入