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单克隆抗体对血小板第4因子抗肝素活性的中和作用。

Neutralization of the antiheparin activity of platelet factor 4 by a monoclonal antibody.

作者信息

Saggin L, Cazzola F, Corona G, Salvatico E, Cella G, Prosdocimi M

机构信息

Dept. of Vascular Biology, Division, FIDIA S.p.A., Abano Terme, Italy.

出版信息

Thromb Haemost. 1992 Jan 23;67(1):137-43.

PMID:1377413
Abstract

We have produced a panel of monoclonal antibodies (mAbs) against rabbit platelet factor 4 (PF4). Two of these mAbs have been characterized in this study. In particular the antibody called 10B2, which also recognizes the human molecule, is able to block PF4's ability to neutralize heparin in a modified Heparin-Factor Xa chromogenic assay. The inhibition appears to be more than 95% at 1:1 mAb/PF4 molar ratio both for purified rabbit and human PF4. Similar results were obtained using supernatants from stimulated human platelets (90% of inhibition at 1:1 mAb/PF4 molar ratio) or using Fab fragments from 10B2. Studies to determine the antigenic determinant against which 10B2 is directed, show that this is an assembled epitope which involves disulfide bonds of the PF4.

摘要

我们制备了一组针对兔血小板因子4(PF4)的单克隆抗体(mAb)。本研究对其中两种单克隆抗体进行了表征。特别是名为10B2的抗体,它也能识别人类分子,在改良的肝素-因子Xa显色测定中能够阻断PF4中和肝素的能力。对于纯化的兔和人PF4,在1:1的单克隆抗体/PF4摩尔比下,抑制率似乎超过95%。使用刺激的人血小板上清液(在1:1的单克隆抗体/PF4摩尔比下抑制率为90%)或使用10B2的Fab片段也获得了类似结果。确定10B2所针对的抗原决定簇的研究表明,这是一个涉及PF4二硫键的组装表位。

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