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曼氏血吸虫:哺乳动物血液成分对尾蚴“穿透”蛋白酶的抑制作用

Schistosoma mansoni: inhibition of cercarial "penetration" proteases by components of mammalian blood.

作者信息

Asch H L, Dresden M H

机构信息

Marrs McLean Department of Biochemistry, Baylor College of Medicine, Houston, TX 77030.

出版信息

Comp Biochem Physiol B. 1977;58(1):89-95. doi: 10.1016/0305-0491(77)90132-8.

Abstract
  1. Normal human sera and plasma were fractionated in order to identify inhibitors of the "penetration" proteases of Schistosoma mansoni cercariae. 2. The main inhibitor, accounting for 90% of the total activity of serum, appears to be alpha 1-antitrypsin (alpha 1-AT) as identified by separation on DEAE-cellulose and Sephadex, by immunoelectrophoresis and by anticercarial protease activity of purified alpha 1-AT preparations. 3. The inhibition profiles of purified preparations of the 6 known serum antiproteases suggest that the parasite protease is similar to vertebrate chymotrypsin. 4. On a molar basis, the order of inhibitory activity against the cercarial protease is: alpha 1-AT = alpha 2-macroglobulin; C'-1-inactivator; alpha 1-antichymotrypsin. No inhibition was obtained with inter-alpha-inhibitor or antithrombin III.
摘要
  1. 为了鉴定曼氏血吸虫尾蚴“穿透”蛋白酶的抑制剂,对正常人血清和血浆进行了分级分离。2. 通过在二乙氨基乙基纤维素(DEAE - 纤维素)和葡聚糖凝胶上的分离、免疫电泳以及纯化的α1 - 抗胰蛋白酶(α1 - AT)制剂的抗尾蚴蛋白酶活性鉴定,占血清总活性90%的主要抑制剂似乎是α1 - 抗胰蛋白酶(α1 - AT)。3. 6种已知血清抗蛋白酶纯化制剂的抑制谱表明,寄生虫蛋白酶类似于脊椎动物的胰凝乳蛋白酶。4. 以摩尔为基础,对尾蚴蛋白酶的抑制活性顺序为:α1 - AT = α2 - 巨球蛋白;C1 - 灭活剂;α1 - 抗糜蛋白酶。α - 抑制剂或抗凝血酶III未显示出抑制作用。

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