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通过蛇毒和细菌金属蛋白酶对反应位点环进行有限的蛋白水解作用使人血浆丝氨酸蛋白酶抑制剂(丝氨酸蛋白酶抑制剂)失活。

Inactivation of human plasma serine proteinase inhibitors (serpins) by limited proteolysis of the reactive site loop with snake venom and bacterial metalloproteinases.

作者信息

Kress L F

出版信息

J Cell Biochem. 1986;32(1):51-8. doi: 10.1002/jcb.240320106.

Abstract

Human plasma serine proteinase inhibitors (serpins) gradually lost activity when incubated with catalytic amounts of snake venom or bacterial metalloproteinases. Electrophoretic analyses indicated that antithrombin III, C1-inhibitor, and alpha 2-antiplasmin had been converted by limited proteolysis into modified species which retained inhibitory activity. Further proteolytic attack resulted in the formation of inactivated inhibitors; alpha 1-proteinase inhibitor (alpha 1-antitrypsin) and alpha 1-antichymotrypsin were also enzymatically inactivated, but active intermediates were not detected. Sequence analyses indicated that the initial, noninactivating cleavage occurred in the amino-terminal region of the inhibitors. Inactivation resulted in all cases from the limited proteolysis of a single bond near, but not at, the reactive site bond in the carboxy-terminal region of the inhibitors. The results indicate that the serpins have two regions which are susceptible to limited proteolysis--one near the amino-terminal end and another in the exposed reactive site loop of the inhibitor.

摘要

人血浆丝氨酸蛋白酶抑制剂(丝氨酸蛋白酶抑制剂)与催化量的蛇毒或细菌金属蛋白酶一起孵育时,活性会逐渐丧失。电泳分析表明,抗凝血酶III、C1抑制剂和α2 - 抗纤溶酶通过有限的蛋白水解作用转化为保留抑制活性的修饰形式。进一步的蛋白水解攻击导致形成失活的抑制剂;α1 - 蛋白酶抑制剂(α1 - 抗胰蛋白酶)和α1 - 抗糜蛋白酶也被酶促失活,但未检测到活性中间体。序列分析表明,最初的非失活切割发生在抑制剂的氨基末端区域。在所有情况下,失活都是由于抑制剂羧基末端区域靠近但不在活性位点键处的单个键的有限蛋白水解作用引起的。结果表明,丝氨酸蛋白酶抑制剂有两个易受有限蛋白水解作用影响的区域——一个靠近氨基末端,另一个在抑制剂暴露的活性位点环中。

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