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Biology of Reproduction 61, 428-435 (1999)
©Copyright 1999 Society for the Study of Reproduction, Inc.


Articles

Sperm Mitochondria-Associated Cysteine-Rich Protein (SMCP) Is an Autoantigen in Lewis Rats1

John C. Herr2,a,c, David Thomasa, Leigh Ann Busha,c, Scott Coonroda,c, Vrinda Khole3,a,c, Stuart S. Howardsb,c, and Charles J. Flickingera,c

a Department of Cell Biology, b Department of Urology, and c The Center for Recombinant Gamete Contraceptive Vaccinogens, University of Virginia, Charlottesville, Virginia 22908

A common repertoire of rat sperm antigens have previously been identified by Western blotting of sperm proteins with sera obtained after vasectomy or isoimmunization with sperm. Aside from a determination of their apparent masses, however, the biochemical characteristics of these antigens have remained unknown. In this study, a rat testis cDNA expression library was screened with polyclonal antibodies obtained from rats immunized with isologous spermatozoa to identify and sequence a full-length clone encoding rat sperm mitochondria-associated cysteine-rich protein (SMCP). The open reading frame of SMCP was expressed in the pET22b vector, and recombinant SMCP (rec-SMCP) was purified. Sera from rats that had been vasectomized or hyperimmunized with isologous sperm specifically recognized rec-SMCP whereas preimmune sera from these experimental groups did not react. Rabbit antiserum produced to rec-SMCP recognized rec-SMCP on Western blots and precisely immunolocalized SMCP to the mid-piece of rat sperm. On Western blots against sperm extracts, the rabbit antibody recognized a major protein band of approximately 22–25 kDa that co-migrated with bands of identical mass that were recognized by sera from hyperimmune or vasectomized rats. These findings demonstrate that SMCP is a sperm autoantigen, recognized following vasectomy, and an isoantigen, recognized by antibodies generated through isologous immunization with sperm.

1 Supported by the NIH-HD U54–29099, P30–28934, P50-DK45179; the Andrew W. Mellon Foundation; and Schering AG.

2 Correspondence: John C. Herr, Department of Cell Biology, University of Virginia, Box 439, Health Sciences Center, Charlottesville, VA 22908. FAX: 804 982 3912; jch7k{at}virginia.edu

3 Current address: Vrinda Khole, Institute for Research in Reproduction (ICMR), JM Street, Mumbai, India.




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