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 3 巻 1 号
23- 頁
2005-08 発行
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1477-7827-3-23.pdf
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種類 :
全文
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タイトル ( eng ) |
Studies on substantially increased proteins in follicular fluid of bovine ovarian follicular cysts using 2-D PAGE and MALDI-TOF MS.
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作成者 |
Maniwa Jiro
Izumi Shunsuke
Terada Takato
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収録物名 |
Reproductive biology and endocrinology
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巻 | 3 |
号 | 1 |
開始ページ | 23 |
抄録 |
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.
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NDC分類 |
生物科学・一般生物学 [ 460 ]
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言語 |
英語
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資源タイプ | 学術雑誌論文 |
出版者 |
BioMed Central
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発行日 | 2005-08 |
権利情報 |
Copyright (c) 2005 by Authors
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出版タイプ | Version of Record(出版社版。早期公開を含む) |
アクセス権 | オープンアクセス |
収録物識別子 |
[DOI] 10.1186/1477-7827-3-23
[ISSN] 1477-7827
[PMID] 15941490
[DOI] http://dx.doi.org/10.1186/1477-7827-3-23
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