Yamamoto T, Sumi H, Maruyama M, Mizumoto H, Ikeda R, Yoshihara H, Mihara H
Clin Chim Acta. 1986 Jul 15;158(1):91-8. doi: 10.1016/0009-8981(86)90119-1.
Acid stable trypsin inhibitor having the same antigenicity as urinary trypsin inhibitor was first identified in the bile of patients with malignant tumors (biliary tract carcinoma or pancreas head carcinoma) and gallstones. Bile trypsin inhibitor from malignant tumor patients was partially purified by DEAE cellulose ion exchange column chromatography. Two molecular forms of the inhibitor were identified. The main form had a molecular weight of about 86,000 and the minor one a molecular weight of 31,000 as determined by gel filtration. Using isoelectric focussing, the larger molecular form gave a pI value of 2.0 and the smaller form, a pI value of 5.1. The isolated larger form migrated on the slightly cationic side of human serum albumin by analytical polyacrylamide gel electrophoresis. The larger form reacted and fused with anti-urinary trypsin inhibitor serum and strongly inhibited trypsin, partially inhibited chymotrypsin and plasmin, but did not inhibit urokinase. The clinical significance of acid stable trypsin inhibitor is discussed.
与尿胰蛋白酶抑制剂具有相同抗原性的酸稳定胰蛋白酶抑制剂最初是在患有恶性肿瘤(胆管癌或胰头癌)和胆结石的患者胆汁中发现的。来自恶性肿瘤患者的胆汁胰蛋白酶抑制剂通过DEAE纤维素离子交换柱色谱法进行了部分纯化。鉴定出该抑制剂的两种分子形式。通过凝胶过滤测定,主要形式的分子量约为86,000,次要形式的分子量为31,000。使用等电聚焦法,较大分子形式的pI值为2.0,较小形式的pI值为5.1。通过分析聚丙烯酰胺凝胶电泳,分离出的较大形式在人血清白蛋白的稍阳离子侧迁移。较大形式与抗尿胰蛋白酶抑制剂血清发生反应并融合,强烈抑制胰蛋白酶,部分抑制糜蛋白酶和纤溶酶,但不抑制尿激酶。本文讨论了酸稳定胰蛋白酶抑制剂的临床意义。