Proteomic Analysis of Bovine Pregnancy-specific Serum Proteins by 2D Fluorescence Difference Gel Electrophoresis

Two dimensional-fluorescence difference gel electrophoresis (2D DIGE) is an emerging technique for comparative proteomics, which improves the reproducibility and reliability of differential protein expression analysis between samples. The purpose of this study was to investigate bovine pregnancy-spe...

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Veröffentlicht in:Asian-Australasian journal of animal sciences. - 1998. - 28(2015), 6 vom: 01. Juni, Seite 788-95
1. Verfasser: Lee, Jae Eun (VerfasserIn)
Weitere Verfasser: Lee, Jae Young, Kim, Hong Rye, Shin, Hyun Young, Lin, Tao, Jin, Dong Il
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2015
Zugriff auf das übergeordnete Werk:Asian-Australasian journal of animal sciences
Schlagworte:Journal Article 2D DIGE Bovine Pregnancy CyDye Pregnancy-specific Serum Proteins Proteomics
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520 |a Two dimensional-fluorescence difference gel electrophoresis (2D DIGE) is an emerging technique for comparative proteomics, which improves the reproducibility and reliability of differential protein expression analysis between samples. The purpose of this study was to investigate bovine pregnancy-specific proteins in the proteome between bovine pregnant and non-pregnant serum using DIGE technique. Serums of 2 pregnant Holstein dairy cattle at day 21 after artificial insemination and those of 2 non-pregnant were used in this study. The pre-electrophoretic labeling of pregnant and non-pregnant serum proteins were mixed with Cy3 and Cy5 fluorescent dyes, respectively, and an internal standard was labeled with Cy2. Labeled proteins with Cy2, Cy3, and Cy5 were separated together in a single gel, and then were detected by fluorescence image analyzer. The 2D DIGE method using fluorescence CyDye DIGE flour had higher sensitivity than conventional 2D gel electrophoresis, and showed reproducible results. Approximately 1,500 protein spots were detected by 2D DIGE. Several proteins showed a more than 1.5-fold up and down regulation between non-pregnant and pregnant serum proteins. The differentially expressed proteins were identified by MALDI-TOF mass spectrometer. A total 16 protein spots were detected to regulate differentially in the pregnant serum, among which 7 spots were up-regulated proteins such as conglutinin precursor, modified bovine fibrinogen and IgG1, and 6 spots were down-regulated proteins such as hemoglobin, complement component 3, bovine fibrinogen and IgG2a three spots were not identified. The identified proteins demonstrate that early pregnant bovine serum may have several pregnancy-specific proteins, and these could be a valuable information for the development of pregnancy-diagnostic markers in early pregnancy bovine serum 
650 4 |a Journal Article 
650 4 |a 2D DIGE 
650 4 |a Bovine Pregnancy 
650 4 |a CyDye 
650 4 |a Pregnancy-specific Serum Proteins 
650 4 |a Proteomics 
700 1 |a Lee, Jae Young  |e verfasserin  |4 aut 
700 1 |a Kim, Hong Rye  |e verfasserin  |4 aut 
700 1 |a Shin, Hyun Young  |e verfasserin  |4 aut 
700 1 |a Lin, Tao  |e verfasserin  |4 aut 
700 1 |a Jin, Dong Il  |e verfasserin  |4 aut 
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