東華大學圖書館 |

語系: 繁體中文

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

Protein identification and peptide s...

Barrett-Wilt, Gregory Alan.

FindBook

Google Book

Amazon

博客來

Protein identification and peptide sequencing: Applications of biological mass spectrometry.

紀錄類型:	書目-語言資料,印刷品 : Monograph/item
正題名/作者:	Protein identification and peptide sequencing: Applications of biological mass spectrometry./
作者:	Barrett-Wilt, Gregory Alan.
面頁冊數:	174 p.
附註:	Adviser: Donald F. Hunt.
Contained By:	Dissertation Abstracts International64-01B.
標題:	Chemistry, Analytical. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3077310
ISBN:	0493977996

Protein identification and peptide sequencing: Applications of biological mass spectrometry.
Barrett-Wilt, Gregory Alan.

Protein identification and peptide sequencing: Applications of biological mass spectrometry. - 174 p.

Adviser: Donald F. Hunt.

Thesis (Ph.D.)--University of Virginia, 2003.

In the current work, mass spectrometry has been employed for peptide sequencing and protein identification in three diverse systems, demonstrating the value of mass spectrometry as a tool for discovery.

ISBN: 0493977996Subjects--Topical Terms:

586156
Chemistry, Analytical.

Protein identification and peptide sequencing: Applications of biological mass spectrometry.
LDR:03446nam 2200325 a 45 001 934688
005 20110509
008 110509s2003 eng d
020 $a 0493977996
035 $a (UnM)AAI3077310
035 $a AAI3077310
040 $a UnM $c UnM
100 1 $a Barrett-Wilt, Gregory Alan. $3 1258387
245 1 0 $a Protein identification and peptide sequencing: Applications of biological mass spectrometry.
300 $a 174 p.
500 $a Adviser: Donald F. Hunt.
500 $a Source: Dissertation Abstracts International, Volume: 64-01, Section: B, page: 0175.
502 $a Thesis (Ph.D.)--University of Virginia, 2003.
520 $a In the current work, mass spectrometry has been employed for peptide sequencing and protein identification in three diverse systems, demonstrating the value of mass spectrometry as a tool for discovery.
520 $a Mass spectrometry is now well-established as a powerful tool for protein and peptide analysis, possessing both high sensitivity—with the ability to detect sequence-informative signals from as little as 50 attomoles of material—and great specificity—a single species can be isolated from a background of thousands of co-existing species.
520 $a The techniques of nano-flow RP-HPLC and micro-electrospray quadrupole ion trap mass spectrometry have been applied to the study of three biological systems. In the first, gel electrophoresis was used to resolve proteins co-immunoprecipitating with the Aurora B mitotic kinase from <italic>Xenopus laevis</italic> egg extracts. Aurora B plays critical regulatory roles in cell division, and has been implicated in the development of cancer in humans. Proteolysis <italic> in situ </italic> with trypsin, followed by mass spectrometry, allowed the identification of both known and novel molecular partners of Aurora B. A novel interaction between Aurora B and dynactin was discovered and verified biochemically.
520 $a In the second study, a molecular sequestration technique was employed to isolate substrates of the <italic>Escherichia coli</italic> proteolytic complexes ClpAP and ClpXP. These proteases are primary routes of bacterial protein degradation, targeting unfolded or missynthesized proteins and regulating cellular levels of specific substrates. We have identified several candidate substrates of ClpXP and ClpAP, and provide preliminary evidence for a possible motif for substrate recognition by the ClpXP protease.
520 $a In the third study, methodology is described for sequencing and identification of the repertoire of peptides presented on B cells by the class I major histocompatibility complex molecule HLA-A*0201. The class I MHC proteins display to the cellular immune system peptide fragments of expressed proteins. This provides protection against intracellular pathogens. We have employed multiple rounds of RP-HPLC fractionation and HPLC/MS to create a database of 685 HLA-A*0201-associated peptides. These peptides have been analyzed from both structural and cellular standpoints. Peptide structural features are described in the context of the crystal structure of HLA-A*0201, and cellular features are also discussed.
590 $a School code: 0246.
650 4 $a Chemistry, Analytical. $3 586156
650 4 $a Chemistry, Biochemistry. $3 1017722
690 $a 0486
690 $a 0487
710 2 0 $a University of Virginia. $3 645578
773 0 $t Dissertation Abstracts International $g 64-01B.
790 $a 0246
790 1 0 $a Hunt, Donald F., $e advisor
791 $a Ph.D.
792 $a 2003
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3077310