Isobe M, Ogita Z
J Exp Zool. 1984 Jul;231(1):19-26. doi: 10.1002/jez.1402310104.
Zymogen-activating factors in the mouse were investigated by two-dimensional electrophoresis. Mouse pancreatic zymogens--trypsinogen-I group (Try G-I group), trypsinogen-II (Try G-II), and chymotrypsinogen (Chy G)--were purified using DEAE-cellulose column chromatography. Analysis by two-dimensional electrophoresis, using the purified zymogens as substrates, revealed enterokinase isozymes and chymotrypsinogen-activating factors in both the intestinal extract and luminal fluid. Mouse enterokinase was separated into at least two bands in the first-dimensional gel, each able to activate both trypsinogens Try G-I group and Try G-II. Chymotrypsinogen-activating factors were separated into several bands in the first-dimensional gel. Some activating factors showed mobilities similar to those of mouse enterokinase isozymes. Moreover, other activating factors that can activate chymotrypsinogen were present only in the more anodal area of the first-dimensional gel. These findings indicate that at least two enterokinases and several chymotrypsinogen-activating factors play an important role in the process of activating digestive enzymes.
通过二维电泳对小鼠中的酶原激活因子进行了研究。使用DEAE - 纤维素柱色谱法纯化小鼠胰腺酶原——胰蛋白酶原I组(Try G - I组)、胰蛋白酶原II(Try G - II)和糜蛋白酶原(Chy G)。以纯化的酶原为底物进行二维电泳分析,结果显示在肠提取物和肠腔液中均存在肠激酶同工酶和糜蛋白酶原激活因子。在第一维凝胶中,小鼠肠激酶至少被分离成两条带,每条带都能够激活胰蛋白酶原Try G - I组和Try G - II。糜蛋白酶原激活因子在第一维凝胶中被分离成几条带。一些激活因子的迁移率与小鼠肠激酶同工酶的迁移率相似。此外,其他能够激活糜蛋白酶原的激活因子仅存在于第一维凝胶的更阳极区域。这些发现表明,至少两种肠激酶和几种糜蛋白酶原激活因子在消化酶激活过程中起重要作用。