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C3分子通过硫酯键裂解产生的SH残基与膜结合,可启动补体激活。

Binding of C3 molecules to membranes via the SH-residue generated by the cleavage of a thioester bond can initiate complement activation.

作者信息

Okada N, Yasuda T, Okada H

机构信息

Department of Microbiology, Fukuoka University School of Medicine, Japan.

出版信息

Biochem Biophys Res Commun. 1988 Mar 15;151(2):743-8. doi: 10.1016/s0006-291x(88)80343-7.

Abstract

Dithiopyridine (DTP)-dipalmitoylphosphatidylethanolamine (DTP-DPPE) was incorporated into liposome membranes to prepare DTP-liposomes. The DTP-liposomes could be lysed by reaction with the alternative complement pathway of any kind of serum tested. Activation of the alternative complement pathway has been shown to be mediated by the binding of C3 molecules to DTP on the liposomes via the SH-residue generated by the cleavage of thioester bond in the alpha-chain of the molecules.

摘要

将二硫代吡啶(DTP)-二棕榈酰磷脂酰乙醇胺(DTP-DPPE)掺入脂质体膜中以制备DTP脂质体。DTP脂质体可通过与任何测试血清的替代补体途径反应而裂解。已表明替代补体途径的激活是由C3分子通过分子α链中硫酯键裂解产生的SH残基与脂质体上的DTP结合介导的。

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