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β2糖蛋白1(β2GP1)增强心磷脂结合活性,但不是抗磷脂抗体的抗原。

Beta 2-glycoprotein 1 (beta 2GP1) enhances cardiolipin binding activity but is not the antigen for antiphospholipid antibodies.

作者信息

Pierangeli S S, Harris E N, Davis S A, DeLorenzo G

机构信息

Antiphospholipid Standardization Laboratory, University of Louisville, Kentucky.

出版信息

Br J Haematol. 1992 Nov;82(3):565-70. doi: 10.1111/j.1365-2141.1992.tb06468.x.

Abstract

Some investigators have reported that a serum protein, beta 2-glycoprotein 1 (beta 2GP1), either alone or in combination with negatively charged phospholipid, may be the antigen for anticardiolipin (aCL) antibodies. To examine these reports further, ELISA tests, inhibition experiments, Ouchterlony and Western blot techniques were used to examine anticardiolipin binding to beta 2GP1. Sera from patients with the antiphospholipid syndrome (APS) and syphilis were studied, as well as whole IgG immunoglobulin and affinity purified (a.p.) IgG aCL antibodies. Results showed no binding of aCL antibodies to beta 2GP1 in the absence of cardiolipin. beta 2GP1 caused enhanced binding of aCL antibodies to cardiolipin, but this enhancement was not observed in inhibition experiments. Binding to cardiolipin occurred in the absence of beta 2GP1. Enhancement of cardiolipin binding activity by beta 2GP1 was observed for APS, but not for syphilis. We conclude that beta 2GP1 is not the antigen for aCL antibodies, nor is it likely that the antibody recognizes shared beta 2GP1-cardiolipin epitopes. Instead, this protein may make cardiolipin more available for aCL binding on solid surfaces by some yet undefined mechanism. This effect may not extend to aqueous suspensions.

摘要

一些研究者报告称,一种血清蛋白,即β2-糖蛋白1(β2GP1),单独或与带负电荷的磷脂结合时,可能是抗心磷脂(aCL)抗体的抗原。为了进一步研究这些报告,采用酶联免疫吸附测定(ELISA)试验、抑制实验、双向免疫扩散(Ouchterlony)和蛋白质印迹(Western blot)技术来检测抗心磷脂与β2GP1的结合情况。研究了抗磷脂综合征(APS)和梅毒患者的血清,以及完整的IgG免疫球蛋白和亲和纯化的(a.p.)IgG aCL抗体。结果显示,在没有心磷脂的情况下,aCL抗体不与β2GP1结合。β2GP1可增强aCL抗体与心磷脂的结合,但在抑制实验中未观察到这种增强作用。在没有β2GP1的情况下也会发生与心磷脂的结合。β2GP1对心磷脂结合活性的增强作用在APS患者中观察到了,但在梅毒患者中未观察到。我们得出结论,β2GP1不是aCL抗体的抗原,抗体也不太可能识别β2GP1 - 心磷脂的共同表位。相反,这种蛋白质可能通过某种尚未明确的机制使心磷脂在固体表面更易于与aCL结合。这种作用可能不会扩展到水悬浮液中。

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