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长抑素是一种非传统的丝氨酸蛋白酶,可诱导针对蜱虫叮咬的保护性免疫。

Longistatin is an unconventional serine protease and induces protective immunity against tick infestation.

作者信息

Islam M Khyrul, Alim M Abdul, Miyoshi Takeharu, Hatta Takeshi, Yamaji Kayoko, Matsumoto Yasunobu, Fujisaki Kozo, Tsuji Naotoshi

机构信息

Department of Global Agricultural Sciences, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Japan.

出版信息

Mol Biochem Parasitol. 2012 Mar-Apr;182(1-2):45-53. doi: 10.1016/j.molbiopara.2011.12.002. Epub 2011 Dec 21.

Abstract

Classical serine proteases use the conserved Ser/His/Asp catalytic triad to hydrolyze substrates. Here, we show that longistatin, a salivary gland protein with two EF-hand domains from the vector tick Haemaphysalis longicornis, does not have the conserved catalytic triad, but still functions as a serine protease. Longistatin was synthesized in and secreted from the salivary glands of ticks, and is injected into host tissues during the acquisition of blood-meals. Longistatin hydrolyzed fibrinogen, an essential plasma protein in the coagulation cascade, and activated plasminogen, into its active form plasmin, a serine protease that dissolves fibrin clots. Longistatin efficiently hydrolyzed several serine protease-specific substrates showing its specificity to the amide bond of Arg. Longistatin did not hydrolyze synthetic substrates specific for other groups of proteases. The enzyme was active at a wide range of temperatures and pHs, with the optimum at 37°C and pH 7. Its activity was efficiently inhibited by various serine protease inhibitors such as phenylmethanesulfonyl fluoride (PMSF), aprotinin, antipain, and leupeptin with the estimated IC(50) of 278.57 μM, 0.35 μM, 41.56 μM and 198.86 μM, respectively. In addition, longistatin was also potently inhibited by Zinc (Zn(2+)) in a concentration-dependent manner with an IC(50) value of 275 μM, and the inhibitory effect of Zn(2+) was revived by ethylenediaminetetra acetic acid (EDTA). Immunization studies revealed that longistatin sharply induced high levels of protective IgG antibodies against ticks. Immunization with longistatin reduced repletion of ticks by about 54%, post engorgement body weight by >11% and molting of nymphs by approximately 34%; thus, the vaccination trial was approximately 73% effective against tick infestation. Taken together, our results suggest that longistatin is a new potent atypical serine protease, and may be an interesting candidate for the development of anti-tick vaccines.

摘要

经典的丝氨酸蛋白酶利用保守的丝氨酸/组氨酸/天冬氨酸催化三联体来水解底物。在此,我们表明,长角血蜱唾液腺中一种具有两个EF-手型结构域的唾液腺蛋白长抑素,并不具有保守的催化三联体,但仍发挥丝氨酸蛋白酶的功能。长抑素在蜱的唾液腺中合成并分泌,在蜱吸食血液时注入宿主组织。长抑素能水解纤维蛋白原(凝血级联反应中的一种重要血浆蛋白),并将纤溶酶原激活为其活性形式的纤溶酶(一种溶解纤维蛋白凝块的丝氨酸蛋白酶)。长抑素能有效水解多种丝氨酸蛋白酶特异性底物,显示出其对精氨酸酰胺键的特异性。长抑素不会水解其他蛋白酶类别的合成底物。该酶在很宽的温度和pH范围内都有活性,最适温度为37°C,最适pH为7。其活性能被多种丝氨酸蛋白酶抑制剂有效抑制,如苯甲基磺酰氟(PMSF)、抑肽酶、抗蛋白酶和亮抑肽酶,估计半数抑制浓度(IC50)分别为278.57 μM、0.35 μM、41.56 μM和198.86 μM。此外,锌(Zn2+)也能以浓度依赖的方式有效抑制长抑素,IC50值为275 μM,而乙二胺四乙酸(EDTA)能恢复锌(Zn2+)的抑制作用。免疫研究表明,长抑素能显著诱导高水平的抗蜱保护性IgG抗体。用长抑素免疫可使蜱的饱血率降低约54%,饱血后体重降低>11%,若虫蜕皮率降低约34%;因此,疫苗试验对蜱感染的有效性约为73%。综上所述,我们的结果表明长抑素是一种新型强效非典型丝氨酸蛋白酶,可能是开发抗蜱疫苗的一个有趣候选物。

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