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DNA适配体对凝血酶活性的抑制作用。

Inhibition of thrombin activity with DNA-aptamers.

作者信息

Dobrovolsky A B, Titaeva E V, Khaspekova S G, Spiridonova V A, Kopylov A M, Mazurov A V

机构信息

Russian Cardiology Research-and-Production Complex, Federal Agency for Health Care and Social Development, M. V. Lomonosov Moscow State University, Russia.

出版信息

Bull Exp Biol Med. 2009 Jul;148(1):33-6. doi: 10.1007/s10517-009-0627-7.

Abstract

The effects of two DNA aptamers (oligonucleotides) 15TBA and 31TBA (15- and 31-mer thrombin-binding aptamers, respectively) on thrombin activity were studied. Both aptamers added to human plasma dose-dependently increased thrombin time (fibrin formation upon exposure to exogenous thrombin), prothrombin time (clotting activation by the extrinsic pathway), and activated partial thromboplastin time (clotting activation by the intrinsic pathway). At the same time, these aptamers did not modify amidolytic activity of thrombin evaluated by cleavage of synthetic chromogenic substrate. Aptamers also inhibited thrombin-induced human platelet aggregation. The inhibitory effects of 31TBA manifested at lower concentrations than those of 15TBA in all tests. These data indicate that the studied antithrombin DNA aptamers effectively suppress its two key reactions, fibrin formation and stimulation of platelet aggregation, without modifying active center of the thrombin molecule.

摘要

研究了两种DNA适体(寡核苷酸)15TBA和31TBA(分别为15聚体和31聚体凝血酶结合适体)对凝血酶活性的影响。将这两种适体添加到人体血浆中,凝血酶时间(暴露于外源性凝血酶时的纤维蛋白形成)、凝血酶原时间(外源性途径激活凝血)和活化部分凝血活酶时间(内源性途径激活凝血)均呈剂量依赖性增加。同时,这些适体不会改变通过切割合成显色底物评估的凝血酶的酰胺水解活性。适体还抑制凝血酶诱导的人血小板聚集。在所有测试中,31TBA的抑制作用在比15TBA更低的浓度下表现出来。这些数据表明,所研究的抗凝血酶DNA适体可有效抑制其两个关键反应,即纤维蛋白形成和血小板聚集刺激,而不会改变凝血酶分子的活性中心。

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