药蛭不稳定酶-溶菌酶-2原重组溶栓制剂对马血小板聚集的抑制作用。

A S Rotkina, I V Pronina, V N Lazarev, D N Akhaev, I P Baskova
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引用次数: 0

摘要

的目的。鉴定药用水蛭新型原重组溶栓制剂不稳定酶-溶菌酶-2抑制血小板聚集的能力。方法:失稳酶-溶菌酶基因。ds2 (mlDL-Ds2)在大肠杆菌细胞中得到克隆。重组蛋白在变性条件下使用金属螯合层析分离,然后按照Kurdyumov A.S.等人(2016,Russian Journal of Bioorganic Chemistry, v.42, s. 42-52)描述的程序快速稀释多肽变性。从18匹马的颈静脉中采集了血液。使用Chrono-Log-700和Сhrono-Log-560, USA560, США聚集仪评估不同浓度不稳定酶溶菌酶存在下血小板在富血小板血浆(PRP)和洗涤血小板悬液(WP)中的聚集状态。作为ADP、III型胶原和人凝血酶的聚集诱导剂。结果:首次证明了新合成的(Kurdyumov A.S. et al. 2016, Russian Journal of Bioorganic Chemistry, v42, s. 42-52)溶血栓重组酶不稳定酶溶酶酶能够抑制超过40%的ADP刺激的PRP聚集和ADP刺激的马血洗血小板聚集。结论:不稳定溶酶酶-2抑制血小板聚集的能力扩展了重组溶栓酶的生物学特性,并于2015年底进行了临床前试验。
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Destabilase-lysozyme-2 - original recombinant thrombolytic preparation of medicinal leech inhibits horse platelets aggregation.

The purpose. Identifying the capacity of the medicinal leech novel original recombinant thrombolytic preparation Destabilase-Lysozyme-2 to inhibit the blood platelet aggregation.

Methods: Gene of destabilase-lysozyme. ds2 (mlDL-Ds2 ), was cloned in E.coli cells. Recombinant protein was isolated in denaturing conditions using metal-chelate chromatography followed by denaturation of the polypeptide by rapid dilution in exact accordance with the procedure described by Kurdyumov A.S. et al. ( 2016, Russian Journal of Bioorganic Chemistry, v.42, s. 42-52). Blood was collected from the jugular vein of 18 horses. The functional status of platelets in the presence of different destabilase-lysozyme concentrations were evaluated for their aggregation in Platelet Rich Plasma ( PRP) and in Washed Platelet suspension (WP) using aggregometers Chrono-Log-700 and Сhrono-Log-560, USA560, США. As used aggregation inducers of ADP, collagen type III and human thrombin.

Results: First demonstrated the ability of newly synthesized (Kurdyumov A.S. et al. 2016, Russian Journal of Bioorganic Chemistry, v42, s. 42-52) thrombolytic recombinant enzyme destabilase-lyzosyme to inhibit more than 40% of ADP-stimulated PRP aggregation and ADP- stimulated aggregation of horse blood washed platelets.

Conclusion: The ability of destabilase-lyzosyme -2 to inhibit platelets aggregation extends biological properties of recombinant thrombolytic enzyme, pre-clinical trials which resulted in the end of 2015.

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