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首页> 外文期刊>Infection and immunity >Receptors for human plasminogen on gram-negative bacteria.
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Receptors for human plasminogen on gram-negative bacteria.

机译:革兰氏阴性细菌上人纤溶酶原的受体。

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A total of 188 strains representing 11 species of gram-negative bacteria were examined for the ability to interact with human plasminogen. Highly purified human plasminogen was labeled with 125I, and its uptake by different bacterial strains was measured. All 14 strains of Haemophilus influenzae and all 13 strains of Branhamella catarrhalis tested were positive with respect to plasminogen uptake. Also, eight species belonging to the family Enterobacteriaceae were tested, and of those, Proteus mirabilis demonstrated the most substantial uptake, with 28 of 39 strains taking up more than 10% of the plasminogen. Ten strains of Pseudomonas aeruginosa were also tested, of which seven showed uptake values higher than 10%. With H. influenzae and B. catarrhalis strains, Scatchard analysis indicated a two-phase receptor interaction, one more-avid receptor with a Kd of 6 to 8 nM and 2,000 to 2,500 sites per bacterium and a second receptor with a Kd of 50 to 80 nM and 9,000 sites per bacterium. With Pseudomonas aeruginosa strains, a single receptor interaction was detected with a Kd of 60 nM and the number of sites was estimated as 8,000 per bacterium. Scatchard analysis with strains of P. mirabilis indicated binding of a less-specific nature. However, plasminogen uptake by this species could be reduced by 50% by the addition of 2 mM unlabeled plasminogen. This estimate of Kd, as well as uptake studies with plasminogen fragments, suggests different properties of this receptor. With all receptor types, the addition of plasmin-aprotinin complex inhibited plasminogen uptake, which demonstrates that both forms of the molecule react with the same receptors. Plasminogen uptake could be eliminated by the addition of lysine or epsilon-aminocaproic acid, which suggests that the lysine-binding sites of the plasminogen molecule are involved in the receptor-ligand interaction.
机译:共检查了代表11种革兰氏阴性细菌的188个菌株与人纤溶酶原相互作用的能力。用125 I标记高度纯化的人纤溶酶原,并测量其被不同细菌菌株吸收的程度。所测试的所有14株流感嗜血杆菌和所有13株卡他氏布拉曼菌的纤溶酶原摄取均为阳性。此外,测试了肠杆菌科的八种菌种,其中奇异变形杆菌显示出最大量的吸收,在39个菌株中,有28种占据了纤溶酶原的10%以上。还测试了十个铜绿假单胞菌菌株,其中七个显示出高于10%的摄取值。 Scatchard分析表明,对于流感嗜血杆菌和卡他芽孢杆菌,两相受体相互作用,一种更重的受体,每个细菌的Kd为6至8 nM,2,000至2,500个位点,第二种受体的Kd为50至200。每个细菌80 nM和9,000个位点。对于铜绿假单胞菌菌株,检测到单受体相互作用,Kd为60 nM,每个细菌的位点数估计为8,000。用奇异假单胞菌菌株的Scatchard分析表明结合的特异性较低。但是,通过添加2 mM未标记的纤溶酶原,该物种吸收的纤溶酶原可降低50%。对Kd的这种估计以及对纤溶酶原片段的吸收研究表明,该受体具有不同的特性。对于所有类型的受体,纤溶酶-抑肽酶复合物的添加都会抑制纤溶酶原的摄取,这表明分子的两种形式都与相同的受体反应。可以通过添加赖氨酸或ε-氨基己酸消除纤溶酶的摄取,这表明纤溶酶原分子的赖氨酸结合位点参与受体-配体相互作用。

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