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Novel monoclonal antibody to fibrin(ogen) αC-region for detection of the earliest forms of soluble fibrin

机译:用于检测最早形式的可溶性纤维蛋白的纤维蛋白(ELIGOLIGE)αC区的新型单克隆抗体

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Obtaining new monoclonal antibodies (mAbs) towards fibrin(ogen) and its fragments is an important task for studying mechanisms of blood clot formation, searching for novel antithrombotic agents and developing immunodiagnostics. The aim of the present work was to create and characterize a new mAb towards the fibrin(ogen) αС-region. We surmise that having a specific mAb towards this flexible part of the molecule will allow us to study the role of the αС-region in fibrin polymerization and also to develop an approach for detecting the earliest forms of soluble fibrin by sandwich ELISA. Using hybridoma technology we оbtained mAb 1-5A to the αC-region of fibrinogen.. It was characterized using several variations of ELISA and Western blot. Application of specific proteases together with MALDI-TOF analysis allowed us to localize its epitope that is located in fragment 537-595 of the Aα-chain of fibrin(ogen). МAb 1-5A can be used as a detecting tag-antibody in sandwich ELISA for the quantification of the earliest forms of soluble fibrin which are uncleaved by plasmin and preserved C-terminal portions of αC-regions. These earliest forms of soluble fibrin are direct evidence of blood coagulation system activation, thrombin generation and the danger of intravascular thrombus formation. Their determination will provide additional, more accurate information about the state of the blood coagulation system and the risk of blood clotting, which is very important for the timely and correct selection of adequate antithrombotic therapy. MAb 1-5A effectively binds the αC-containing molecules of fibrinogen and fibrin in blood plasma. It also can be used for studying protein-protein and protein-cellular interactions of the αC-regions of fibrin(ogen).
机译:获得新的单克隆抗体(MAB)朝向纤维蛋白(ELOGION)及其片段是研究血凝块形成的机制的重要任务,寻找新的抗血栓形成剂和发展免疫诊断。本作本作的目的是创造和表征朝向纤维蛋白(ELOGEN)αС区的新MAB。我们推测,具有朝向这种柔性部分的特异性mAb将允许我们研究αС区在纤维蛋白聚合中的作用,也可以通过夹心ELISA制定检测最早形式的可溶性纤维蛋白的方法。使用杂交瘤技术,我们对纤维蛋白原的αC区域进行了MAB 1-5a。它的特征在于使用ELISA和Western印迹的几种变化。特异性蛋白酶的应用与MALDI-TOF分析允许我们本地化其位于纤维蛋白(ELIGOL)的Aα链的片段537-595中的表位。 Мab1-5a可用作夹层ELISA中的检测标签抗体,用于定量最早形式的可溶性纤维蛋白,其通过纤溶酶未脱切并保存αc-区的C末端部分。这些最早形式的可溶性纤维蛋白是血液凝固系统活化,凝血酶产生和血管内血栓形成危险的直接证据。他们的决心将提供有关血液凝固系统状态和血液凝固风险的额外,更准确的信息,这对于及时和正确选择适当的抗血栓性治疗非常重要。 MAB 1-5A有效地结合血浆中含αC的纤维蛋白原和纤维蛋白。它还可用于研究纤维蛋白(ELIGOL)αC区的蛋白质 - 蛋白质和蛋白质 - 细胞相互作用。

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