Language:
English
繁體中文
Help
回圖書館首頁
手機版館藏查詢
Login
Back
Switch To:
Labeled
|
MARC Mode
|
ISBD
Gene delivery modulated by redox pot...
~
Soundara Manickam, Devika.
Linked to FindBook
Google Book
Amazon
博客來
Gene delivery modulated by redox potential gradients.
Record Type:
Electronic resources : Monograph/item
Title/Author:
Gene delivery modulated by redox potential gradients./
Author:
Soundara Manickam, Devika.
Description:
109 p.
Notes:
Source: Masters Abstracts International, Volume: 44-03, page: 1376.
Contained By:
Masters Abstracts International44-03.
Subject:
Chemistry, Pharmaceutical. -
Online resource:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=1430529
ISBN:
9780542434341
Gene delivery modulated by redox potential gradients.
Soundara Manickam, Devika.
Gene delivery modulated by redox potential gradients.
- 109 p.
Source: Masters Abstracts International, Volume: 44-03, page: 1376.
Thesis (M.S.)--Wayne State University, 2005.
The existence of a high redox potential gradient across the cellular membranes offers an advantageous stimulus for the programmed delivery of genes. In this project, we have synthesized vectors sensitive to redox potential gradients, which have proven their ability to deliver genes with high transfection efficiency and minimal cytotoxicity. Bioactive peptide sequences have demonstrated their natural ability to translocate across cell membranes and to deliver DNA to the nucleus of the target cells. A high molecular weight homopolypeptide was synthesized based on the TAT peptide; a protein transduction domain derived from the transactivating transcriptional activator protein from HIV-1 and for the first time, a high molecular weight copolypeptide was synthesized by randomly linking two different peptide sequences: a nuclear localization sequence peptide derived from the SV40 virus and a histidine rich buffering peptide. Physical properties and biological activity of the polycation/DNA complexes were studied. The results demonstrate that carriers based on these bioactive peptide sequences possess high transfection activity in the tested cell lines and exhibit minimal to negligible cytotoxicity in the human endothelial cells. These observations encourage examining the suitability of these carriers for in vivo gene delivery. (Abstract shortened by UMI.)
ISBN: 9780542434341Subjects--Topical Terms:
550957
Chemistry, Pharmaceutical.
Gene delivery modulated by redox potential gradients.
LDR
:02207nmm 2200277 4500
001
1820845
005
20061103104858.5
008
130610s2005 eng d
020
$a
9780542434341
035
$a
(UnM)AAI1430529
035
$a
AAI1430529
040
$a
UnM
$c
UnM
100
1
$a
Soundara Manickam, Devika.
$3
1910049
245
1 0
$a
Gene delivery modulated by redox potential gradients.
300
$a
109 p.
500
$a
Source: Masters Abstracts International, Volume: 44-03, page: 1376.
500
$a
Adviser: David Oupicky.
502
$a
Thesis (M.S.)--Wayne State University, 2005.
520
$a
The existence of a high redox potential gradient across the cellular membranes offers an advantageous stimulus for the programmed delivery of genes. In this project, we have synthesized vectors sensitive to redox potential gradients, which have proven their ability to deliver genes with high transfection efficiency and minimal cytotoxicity. Bioactive peptide sequences have demonstrated their natural ability to translocate across cell membranes and to deliver DNA to the nucleus of the target cells. A high molecular weight homopolypeptide was synthesized based on the TAT peptide; a protein transduction domain derived from the transactivating transcriptional activator protein from HIV-1 and for the first time, a high molecular weight copolypeptide was synthesized by randomly linking two different peptide sequences: a nuclear localization sequence peptide derived from the SV40 virus and a histidine rich buffering peptide. Physical properties and biological activity of the polycation/DNA complexes were studied. The results demonstrate that carriers based on these bioactive peptide sequences possess high transfection activity in the tested cell lines and exhibit minimal to negligible cytotoxicity in the human endothelial cells. These observations encourage examining the suitability of these carriers for in vivo gene delivery. (Abstract shortened by UMI.)
590
$a
School code: 0254.
650
4
$a
Chemistry, Pharmaceutical.
$3
550957
650
4
$a
Chemistry, Biochemistry.
$3
1017722
690
$a
0491
690
$a
0487
710
2 0
$a
Wayne State University.
$3
975058
773
0
$t
Masters Abstracts International
$g
44-03.
790
1 0
$a
Oupicky, David,
$e
advisor
790
$a
0254
791
$a
M.S.
792
$a
2005
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=1430529
based on 0 review(s)
Location:
ALL
電子資源
Year:
Volume Number:
Items
1 records • Pages 1 •
1
Inventory Number
Location Name
Item Class
Material type
Call number
Usage Class
Loan Status
No. of reservations
Opac note
Attachments
W9211708
電子資源
11.線上閱覽_V
電子書
EB
一般使用(Normal)
On shelf
0
1 records • Pages 1 •
1
Multimedia
Reviews
Add a review
and share your thoughts with other readers
Export
pickup library
Processing
...
Change password
Login