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纤维蛋白原曼彻斯特中异常纤维蛋白肽A的延迟释放:Aα16位精氨酸被组氨酸取代对纤维蛋白单体聚合的影响以及该肽的免疫交叉反应性。

Delayed release of an abnormal fibrinopeptide A from fibrinogen Manchester: effect of the A alpha 16 Arg leads to His substitution upon fibrin monomer polymerization and the immunological crossreactivity of the peptide.

作者信息

Lane D A, Southan C, Ireland H, Thompson E, Kehl M, Henschen A

出版信息

Br J Haematol. 1983 Apr;53(4):587-97. doi: 10.1111/j.1365-2141.1983.tb07310.x.

Abstract

Fibrinogen Manchester is an abnormal fibrinogen with an impaired release of fibrinopeptide A (FPA) and a polymerization abnormality. In the accompanying article we have identified the amino acid substitution in fibrinogen Manchester as A alpha 16 Arg leads to His. When fibrinogen Manchester was digested with low thrombin concentrations approximately 40-50% of the total FPA content was release at a rate similar to FPA release from normal fibrinogen. The fibrin so formed exhibited an impaired polymerization of monomers. Digestion of fibrinogen Manchester with high concentrations of thrombin for prolonged times released the remaining FPA which had an abnormal retention time when studied by high performance liquid chromatography (HPLC). This fibrinopeptide has been shown previously to contain the A alpha 16 Arg leads to His substitution. fibrin resulting from this exhaustive digestion had normal polymerization of monomers. The normal and substituted FPAs were isolated by HPLC and compared in a double antibody competitive-binding assay for normal FPA. The immunological cross-reactivity of the abnormal peptide was reduced, so that approximately 5 times more abnormal peptide was required on a molar basis to displace labelled normal FPA. Normal intact fibrinogen was 10-fold less reactive (on a half molar basis) than free normal FPA and the crossreactivity of fibrinogen Manchester was measurably less than that of normal fibrinogen. It is concluded that immunological measurement alone of FPA released from abnormal fibrinogens may not give a complete description of the kinetics of peptide release if the amino acid substitution lies within the FPA sequence. The combination of radioimmunoassay and HPLC, however, provides a powerful analytical approach that should be useful in classifying and characterizing abnormal fibrinogens.

摘要

曼彻斯特纤维蛋白原是一种异常纤维蛋白原,其纤维蛋白肽A(FPA)释放受损且存在聚合异常。在随附的文章中,我们已确定曼彻斯特纤维蛋白原中的氨基酸替代为Aα16位的精氨酸突变为组氨酸。当用低浓度凝血酶消化曼彻斯特纤维蛋白原时,约40 - 50%的总FPA含量以与正常纤维蛋白原释放FPA相似的速率释放。如此形成的纤维蛋白表现出单体聚合受损。用高浓度凝血酶长时间消化曼彻斯特纤维蛋白原会释放出剩余的FPA,通过高效液相色谱(HPLC)研究时,其保留时间异常。此前已证明该纤维蛋白肽含有Aα16位精氨酸突变为组氨酸的替代。这种彻底消化产生的纤维蛋白单体聚合正常。通过HPLC分离出正常和替代的FPA,并在针对正常FPA的双抗体竞争性结合试验中进行比较。异常肽的免疫交叉反应性降低,因此在摩尔基础上需要约5倍以上的异常肽才能取代标记的正常FPA。正常完整纤维蛋白原的反应性(以半摩尔为基础)比游离正常FPA低10倍,且曼彻斯特纤维蛋白原的交叉反应性明显低于正常纤维蛋白原。结论是,如果氨基酸替代位于FPA序列内,仅对异常纤维蛋白原释放的FPA进行免疫测定可能无法完整描述肽释放的动力学。然而,放射免疫测定和HPLC的结合提供了一种强大的分析方法,在对异常纤维蛋白原进行分类和表征方面应该是有用的。

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