Studies on substantially increased proteins in follicular fluid of bovine ovarian follicular cysts using 2-D PAGE and MALDI-TOF MS.

Reproductive biology and endocrinology Volume 3 Issue 1 Page 23- published_at 2005-08
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Title ( eng )
Studies on substantially increased proteins in follicular fluid of bovine ovarian follicular cysts using 2-D PAGE and MALDI-TOF MS.
Creator
Maniwa Jiro
Izumi Shunsuke
Terada Takato
Source Title
Reproductive biology and endocrinology
Volume 3
Issue 1
Start Page 23
Abstract
BACKGROUND: The objective of this study was to identify substantially increased proteins in bovine cystic follicular fluid (FF) in order to clarify the pathology and etiology of bovine ovarian follicular cysts (BOFC). METHODS: Proteins in normal and cystic FF samples were subjected to two-dimensional polyacrylamide gel electrophoresis (2-D PAGE) and were compared using silver stained gel images with PDQuest image analysis software. Peptides from these increased spots were analyzed by matrix assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS), and were identified based on the NCBI database by a peptide mass fingerprinting method. RESULTS: Comparative proteomic analysis showed 8 increased protein spots present in cystic FF. MS analysis and database searching revealed that the increased proteins in cystic FF were bovine mitochondrial f1-atpase (BMFA), erythroid associated factor (EAF), methionine synthase (MeS), VEGF-receptor, glyceraldehydes 3-phosphate dehydrogenase (GAPDH), heat shock protein 70 (HSP70), beta-lactoglobulin (BLG) and succinate dehydrogenase Ip subunit (SD). CONCLUSION: Our results suggest that these proteins are overexpressed in BOFC, and that they may play important roles in the pathogenesis of BOFC. Furthermore, these proteins in the FF could be useful biomarkers for BOFC.
NDC
Biology [ 460 ]
Language
eng
Resource Type journal article
Publisher
BioMed Central
Date of Issued 2005-08
Rights
Copyright (c) 2005 by Authors
Publish Type Version of Record
Access Rights open access
Source Identifier
[DOI] 10.1186/1477-7827-3-23
[ISSN] 1477-7827
[PMID] 15941490
[DOI] http://dx.doi.org/10.1186/1477-7827-3-23