Separation and Identification of Urinary Proteins Following Digital Rectal Examination in Patients with Benign Prostatic Hypertrophy

Q4 Biochemistry, Genetics and Molecular Biology
Y. Usami, K. Iguchi, T. Adachi, Hajime Yamamoto, K. Koshida, T. Uchibayashi, K. Hirano
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引用次数: 0

Abstract

Specimens of urine were obtained before and after digital rectal examination from four patients with benign prostatic hypertrophy (BPH) for comparative analysis of protein components by reversed-phase high performance liquid chromatography. Four characteristic peaks were detected in urine after compared with before the physical examination, and their molecular masses on SDS-polyacrylamide gel electrophoresis were 16, 16, 34 and 46 kDa. After the proteins were reduced, S-pyridylethylated and cleaved with cyanogen bromide, the amino-terminal amino acids were sequenced and a homology search was conducted. The two 16-kDa proteins were both identified as fl-microseminoprotein. The 34-kDa protein was identified as a prostate-specific antigen, and the 46-kDa protein was a Zn-a2-glycoprotein. The present findings provide important information on pre-analytical sampling of urine for the diagnosis of BPH.
良性前列腺肥大患者直肠指检后尿蛋白的分离与鉴定
取4例良性前列腺肥大(BPH)患者直肠指检前后尿液标本,采用反相高效液相色谱法对其蛋白质成分进行对比分析。与体检前比较,尿中检出4个特征峰,sds -聚丙烯酰胺凝胶电泳分子量分别为16、16、34和46 kDa。将蛋白质还原、s -吡啶乙基化和溴化氰裂解后,对其氨基末端氨基酸进行测序和同源性搜索。这两个16 kda的蛋白都被鉴定为fl-microseminoprotein。34-kDa蛋白为前列腺特异性抗原,46-kDa蛋白为zn -a2糖蛋白。本研究结果为前列腺增生症的诊断提供了尿液分析前取样的重要信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Japanese Journal of Clinical Chemistry
Japanese Journal of Clinical Chemistry Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
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