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抗凝组分Acoagulatin的纯化鉴定及其抗凝特性
引用本文:李婷,朱正光,余传林,吴曙光.抗凝组分Acoagulatin的纯化鉴定及其抗凝特性[J].第一军医大学学报,2004,24(7):836-838.
作者姓名:李婷  朱正光  余传林  吴曙光
作者单位:第一军医大学药物研究所,广东广州510515
摘    要:目的 从蝮蛇毒中分离纯化一种组分acoagulatin并进行鉴定。观察其抗凝作用。方法 经DEAE-Sepharose Fast Flow和CM-sepharose Fast Flow离子交换柱层析,从蝮蛇毒中分离、纯化得到acoagulatin,分别采用Biosep-sec-S2000型HPLC分子筛柱层析、还原性SDS-PAGE(5%浓缩胶,12%分离胶)电泳进行纯度和相对分子质量测定,将不同浓度acoagulatin与抗凝兔血混合,测定凝血时间(TT)、凝血酶原时间(PT)、部分凝血活酶时间(APTT)。结果 Acoagulatin的相对分子质量为31400,由两个亚基组成,相对分子质量分别为14400和17000,能显著地延长PT和APTT,对TT没有影响。结论 采用DEAE-Sepharose Fast Flow和CM-sepharose Fast Flow两种离子交换柱层析分离蛇毒,能分离出纯度高的组分acoagulatin,该组分具有抗凝活性。

关 键 词:蛇毒  纯化  凝血时间  凝血酶原时间  部分凝血活酶时间

Purification, identification of acoagulatin, an anticoagulation factor from the venom of Chinese Agkistrodon, and observation of its anticoagulation effect]
Ting Li,Zheng-guang Zhu,Chuan-lin Yu,Shu-guang Wu.Purification, identification of acoagulatin, an anticoagulation factor from the venom of Chinese Agkistrodon, and observation of its anticoagulation effect][J].Journal of First Military Medical University,2004,24(7):836-838.
Authors:Ting Li  Zheng-guang Zhu  Chuan-lin Yu  Shu-guang Wu
Institution:Institute of Parmaceutical Sciences, First Military Medical University, Guangzhou 510515, China. tinglee77@hotmail.com
Abstract:OBJECTIVE: To isolate and identify an anticoagulation factor, acoagulatin, from the venom of Chinese Agkistrodon and to observe its anticoagulation effect. METHOD: The venom of Chinese Agkistrodon was isolated and purified using ion-exchange chromatography on DEAE-Sepharose Fast Flow and CM-sepharose Fast Flow. High-performance liquid chromatography (HPLC) was performed for determination of the purity of acoagulatin, and SDS-PAGE electrophoresis (with 5% concentrated gel of pH 6.8, 12% separation gel of pH 8.8, Tris-aminoacetic acid buffer of pH 8.3 as the electrode buffer) for determining the relative molecular mass. For observation of the anticoagulation effect, 20 microl acoagulatin solution at the concentration of 0.30, 0.20 and 0.15 microg/microl, respectively, was mixed with 100 microl rabbit anticoagulated plasma and the thrombin time (TT), prothrombin time (PT) and activated partial thromboplastin time (APTT) were determined. RESULTS: Acoagulatin was found to consist of two subunits with relative molecular mass of 14 400 and 17 000 respectively, resulting in the total relative molecular mass of 31 400 as determined by SDS-PAGE. HPLC demonstrated good homogeneity of this protein, which significantly prolonged the PT and APTT without affecting TT. CONCLUSION: DEAE-Sepharose Fast Flow and CM-sepharose Fast Flow ion exchange column chromatographies are effective to isolate acoagulatin of high purity, which possesses anticoagulation effect.
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