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
Development of fluorescent/stable is...
~
Pennington, Justin Paul.
Linked to FindBook
Google Book
Amazon
博客來
Development of fluorescent/stable isotope tagging strategies for proteins containing DOPA.
Record Type:
Electronic resources : Monograph/item
Title/Author:
Development of fluorescent/stable isotope tagging strategies for proteins containing DOPA./
Author:
Pennington, Justin Paul.
Description:
231 p.
Notes:
Source: Dissertation Abstracts International, Volume: 67-11, Section: B, page: 6417.
Contained By:
Dissertation Abstracts International67-11B.
Subject:
Chemistry, Analytical. -
Online resource:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3242148
ISBN:
9780542973277
Development of fluorescent/stable isotope tagging strategies for proteins containing DOPA.
Pennington, Justin Paul.
Development of fluorescent/stable isotope tagging strategies for proteins containing DOPA.
- 231 p.
Source: Dissertation Abstracts International, Volume: 67-11, Section: B, page: 6417.
Thesis (Ed.D.)--University of Kansas, 2007.
Oxidative modification of protein tyrosine, including hydroxylation, to form proteins containing DOPA (PC-DOPA), has been associated with many age dependent pathologies. To date, there has been no report of a chemically selective method for in-vivo determination of PC-DOPA. By building upon previous derivatization methods that used benzylamine (BA) or diphenylethylenediamine (DPE) to form highly fluorescent products with catechols and catecholamines, a fluorescent/stable isotope tagging strategy for PC-DOPA was developed. By examination of the products derived from the reaction of small molecule model compounds with DPE and BA reagents, a robust understanding of the reaction process leading to the formation of highly fluorescent substituted benzoxazole products was established. These products were identified by a combination of MS, multi-dimensional NMR, and X-ray crystallography. With this information in hand, it was determined that the use of BA would be more efficient for experiments where isotopic labeling was required, i.e., use of BA with 5 deuterium atoms substituted on the aromatic ring for relative quantitation by MS. Relative quantitation was demonstrated using 4-methylcatechol and DOPA-G-G as model compounds.
ISBN: 9780542973277Subjects--Topical Terms:
586156
Chemistry, Analytical.
Development of fluorescent/stable isotope tagging strategies for proteins containing DOPA.
LDR
:02142nmm 2200277 4500
001
1829350
005
20071107102538.5
008
130610s2007 eng d
020
$a
9780542973277
035
$a
(UMI)AAI3242148
035
$a
AAI3242148
040
$a
UMI
$c
UMI
100
1
$a
Pennington, Justin Paul.
$3
1918213
245
1 0
$a
Development of fluorescent/stable isotope tagging strategies for proteins containing DOPA.
300
$a
231 p.
500
$a
Source: Dissertation Abstracts International, Volume: 67-11, Section: B, page: 6417.
500
$a
Adviser: John F. Stobaugh.
502
$a
Thesis (Ed.D.)--University of Kansas, 2007.
520
$a
Oxidative modification of protein tyrosine, including hydroxylation, to form proteins containing DOPA (PC-DOPA), has been associated with many age dependent pathologies. To date, there has been no report of a chemically selective method for in-vivo determination of PC-DOPA. By building upon previous derivatization methods that used benzylamine (BA) or diphenylethylenediamine (DPE) to form highly fluorescent products with catechols and catecholamines, a fluorescent/stable isotope tagging strategy for PC-DOPA was developed. By examination of the products derived from the reaction of small molecule model compounds with DPE and BA reagents, a robust understanding of the reaction process leading to the formation of highly fluorescent substituted benzoxazole products was established. These products were identified by a combination of MS, multi-dimensional NMR, and X-ray crystallography. With this information in hand, it was determined that the use of BA would be more efficient for experiments where isotopic labeling was required, i.e., use of BA with 5 deuterium atoms substituted on the aromatic ring for relative quantitation by MS. Relative quantitation was demonstrated using 4-methylcatechol and DOPA-G-G as model compounds.
590
$a
School code: 0099.
650
4
$a
Chemistry, Analytical.
$3
586156
650
4
$a
Chemistry, Pharmaceutical.
$3
550957
690
$a
0486
690
$a
0491
710
2 0
$a
University of Kansas.
$3
626626
773
0
$t
Dissertation Abstracts International
$g
67-11B.
790
1 0
$a
Stobaugh, John F.,
$e
advisor
790
$a
0099
791
$a
Ed.D.
792
$a
2007
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3242148
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
W9220213
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