Biol Reprod
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Fouchécourt, S.
Right arrow Articles by Orgebin-Crist, M.-C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Fouchécourt, S.
Right arrow Articles by Orgebin-Crist, M.-C.
Agricola
Right arrow Articles by Fouchécourt, S.
Right arrow Articles by Orgebin-Crist, M.-C.
Biology of Reproduction 66, 524-533 (2002)
© 2002 Society for the Study of Reproduction, Inc.


Regular Article

Epididymal Lipocalin-Type Prostaglandin D2 Synthase: Identification Using Mass Spectrometry, Messenger RNA Localization, and Immunodetection in Mouse, Rat, Hamster, and Monkey1

Sophie Fouchécourta,d, Pierre Chaurandb, Beverly B. DaGueb, Jean-Jacques Lareyrea,d, Robert J. Matusikc,d, Richard M. Capriolib, and Marie-Claire Orgebin-Crist2,a,d

a Departments of Obstetrics and Gynecology, b Biochemistry, c Urologic Surgery, and d Center for Reproductive Biology Research, Vanderbilt University Medical Center, Nashville, Tennessee 37232

This study identified prostaglandin D2 synthase (PGDS) in murine epididymal fluid using a proteomic approach combining two-dimensional (2D) gel electrophoresis and mass spectrometry (MS). The caudal epididymal fluid was collected by retroperfusion, and proteins were separated by 2D gel electrophoresis followed by matrix-assisted laser desorption ionization MS analyses after trypsin digestion. The identification was based on the protein-specific peptide map as well as on sequence information generated by nano-electrospray ionization MS/MS. By in situ hybridization, the mRNA was detected in caput, corpus, and cauda, but it was not detected in the initial segment. The PGDS protein was mostly detected in the corpus and cauda by Western blot analysis and immunohistochemistry using a specific polyclonal antibody. In caudal fluid, PGDS was distributed among several isoforms (pI range, 6.5–8.8), suggesting that this protein undergoes posttranslational modification of its primary sequence. After N-glycanase digestion, the molecular mass decreased from 20–25 to 18.5 kDa, its theoretical mass. The PGDS was also detected in the epididymis of rat, hamster, and cynomolgus monkey from the caput to the cauda. In conclusion, MS is a powerful and accurate technique that allows unambiguous identification of the murine epididymal PGDS. The protein is 1) present throughout the epididymis, except in the initial segment, with an increasing luminal concentration from distal caput to cauda; 2) a major protein in caudal fluid; 3) an N-glycosylated, highly polymorphic protein; and 4) conserved during evolution.

First decision: 5 June 2001.

1 Supported by the Rockefeller/Ernst Shering Foundation and by NIH grants HD 36900 and GM 58008.

2 Correspondence: Marie-Claire Orgebin-Crist, Center for Reproductive Biology Research, Vanderbilt University, School of Medicine, Medical Center North, Room C3306, Nashville, TN 37232-2633. FAX: 615 343 7797; m-c.orgebin-crist{at}mcmail.vanderbilt.edu




This article has been cited by other articles:


Home page
Biol. Reprod.Home page
T. T. Turner, D. S. Johnston, J. N. Finger, and S. A. Jelinsky
Differential Gene Expression among the Proximal Segments of the Rat Epididymis Is Lost after Efferent Duct Ligation
Biol Reprod, July 1, 2007; 77(1): 165 - 171.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
H. Zhu, H. Ma, H. Ni, X.-H. Ma, N. Mills, and Z.-M. Yang
Expression and Regulation of Lipocalin-Type Prostaglandin D Synthase in Rat Testis and Epididymis
Biol Reprod, April 1, 2004; 70(4): 1088 - 1095.
[Abstract] [Full Text] [PDF]


Home page
Clin. Cancer Res.Home page
S. A. Schwartz, R. J. Weil, M. D. Johnson, S. A. Toms, and R. M. Caprioli
Protein Profiling in Brain Tumors Using Mass Spectrometry: Feasibility of a New Technique for the Analysis of Protein Expression
Clin. Cancer Res., February 1, 2004; 10(3): 981 - 987.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
T. G. Cooper, A. Wagenfeld, G. A. Cornwall, N. Hsia, S. T. Chu, M.-C. Orgebin-Crist, J. Drevet, P. Vernet, C. Avram, E. Nieschlag, et al.
Gene and Protein Expression in the Epididymis of Infertile c-ros Receptor Tyrosine Kinase-Deficient Mice
Biol Reprod, November 1, 2003; 69(5): 1750 - 1762.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
S. Fouchecourt, J.-J. Lareyre, P. Chaurand, B. B. DaGue, K. Suzuki, D. E. Ong, G. E. Olson, R. J. Matusik, R. M. Caprioli, and M.-C. Orgebin-Crist
Identification, Immunolocalization, Regulation, and Postnatal Development of the Lipocalin EP17 (Epididymal Protein of 17 Kilodaltons) in the Mouse and Rat Epididymis
Endocrinology, March 1, 2003; 144(3): 887 - 900.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2002 by the Society for the Study of Reproduction.