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Identification, purification and characterization of a novel human blood protein with binding affinity for prostate secretory protein of 94 amino acids.

Authors
  • Reeves, Jonathan R
  • Xuan, Jim W
  • Arfanis, Katerina
  • Morin, Catherine
  • Garde, Seema V
  • Ruiz, Marcia T
  • Wisniewski, Jan
  • Panchal, Chandra
  • Tanner, Jerome E
Type
Published Article
Journal
Biochemical Journal
Publisher
Portland Press
Publication Date
Jan 01, 2005
Volume
385
Issue
Pt 1
Pages
105–114
Identifiers
PMID: 15344909
Source
Medline
License
Unknown

Abstract

PSP94 (prostate secretory protein of 94 amino acids), an abundant protein within semen, has reported local functions within the reproductive tract and reported systemic functions. Mechanisms of action remain poorly understood, but binding to undefined molecules within the prostate, pituitary, testis and blood may initiate some of these actions. PSP94 serum measurements, especially of bound and free forms, have potential clinical utility in prostate cancer management. Identification of the binding molecules will help in the understanding of PSP94's action, and enable further development of PSP94 serum assays. PSPBP (PSP94-binding protein) was purified from human serum by ammonium sulphate fractionation, ion-exchange and affinity chromatography. The glycosylated protein ran as two bands on SDS/PAGE (70 and 95 kDa). N-terminal sequencing yielded a 30-amino-acid sequence, identical with the translated N-terminal region of a previously published cDNA (GenBank accession number AX136261). Reverse transcriptase PCR and plaque hybridization demonstrated PSPBP mRNA in peripheral blood leucocytes and in a prostate cDNA library. Northern blotting showed 2 kb mRNA species in prostate, testis, ovary and intestine. Immunohistochemistry demonstrated PSPBP in tissues, including pituitary and Leydig cells, supporting a role for PSP94 in hormonal control at the pituitary gonadal axis. ELISA demonstrated that PSPBP levels were significantly lower (P=0.0014) in the serum of a prostate cancer population (n=65) compared with a control population (n=70). PSPBP identification will help the understanding of PSP94's functions and facilitate ELISA development to address the clinical value of PSP94 serum assays.

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