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机构地区:[1]中山大学基础医学院药理学教研室,广东广州510080
出 处:《中山大学学报(医学科学版)》2005年第4期404-408,共5页Journal of Sun Yat-Sen University:Medical Sciences
基 金:广东省科技厅计划资助项目(2003A10905)
摘 要:【目的】研究C端序列对非出血重组纤溶酶(rFⅡ)特异性、活性和热敏感性的影响。【方法】通过SOEingPCR方法构建删除C端序列的突变体,突变体和rFⅡ分别在P.pastoris中诱导表达。表达和纯化的蛋白用SDS-PAGE和Westerenblot进行鉴定。之后分析其生化特性。【结果】rFⅡ及突变体通过SDS-PAGE和Westerenblot得到证实。生化分析揭示:①突变体对显色底物N-(p-Tosyl)-Gly-Pro-Lys-pNA的催化效率(Kcat/Km)是rFⅡ的1.9倍;②突变体和rFⅡ对氧化的胰岛素B链拥有共同的优先裂解位点,可是在随后的裂解中开始展现差异;③突变体显示了更高的纤(原)活性;④热处理表明突变体相较rFⅡ对温度的增加更敏感;⑤通过圆二色谱测量,突变体的螺旋比例有所增加。【结论】删除的序列参与rFⅡ的特异性、活性和热敏感性,该序列可作为下一步优化的候选序列。[Objective]To investigate the effect of C-terminal region on the specificity, activity, and heat-sensitivity of nonhemorrhagic recombinant fibrin(ogen)olytic metalloprotease (rFⅡ). [Method]SOEing PCR was used for constructing mutation of deleting the C-terminal region. The mutation and rFⅡ were induced and expressed in transformed P.pastoris cells respectively. The expressed and purified proteins were identified by SDS-PAGE and Western blot analysis. After that, biochemical characteristics were analyzed.[Result]The mutation and rFⅡ were confirmed by SDS-PAGE and Western blot analysis. Biochemical characteristics analysis revealed:(1) Mutation caused 1.9 fold increase of catalytic efficiency (Kcat/Km) against chromogenic substrate (N-(p-Tosyl)-Gly-Pro-Lys-pNA); (2)The mutation and rFⅡ shared common preferential cleavage site(12-13) of oxidized insulin-B chain while the difference started to display at secondary cleavage site; (3) Fibrin(ogn)olytic activity analysis revealed a higher activity in mutation. (4) Heat treatment indicated that mutation was more sensitive than rFⅡ to increase of temperature; (5) Furthermore, the ratio of helix of mutation increased by circular dichroism measurements.[Conclusion]The deleted sequence was involved in specificity, activity, and heat-sensitivity of rFⅡ and could be viewed as a candidate sequence for optimization.
关 键 词:血重组 蛇毒纤溶酶 序列 删除 C端 PASTORIS SDS-PAGE 热敏感性 突变体 blot PCR方法 胰岛素B链 诱导表达 生化特性 生化分析 裂解位点 圆二色谱 特异性 rF 活性 热处理
分 类 号:R544.1[医药卫生—心血管疾病] R973.2[医药卫生—内科学]
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