...
首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >Measurement of the differences in electrophoretic mobilities of individual molecules of E. coli beta-galactosidase provides insight into structural differences which underlie enzyme microheterogeneity.
【24h】

Measurement of the differences in electrophoretic mobilities of individual molecules of E. coli beta-galactosidase provides insight into structural differences which underlie enzyme microheterogeneity.

机译:大肠杆菌β-半乳糖苷酶单个分子的电泳迁移率差异的测量提供了洞察酶微异质性基础的结构差异。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

The electrophoretic mobility and catalytic activity of individual molecules of Escherichia coli beta-galactosidase were measured using CE-LIF detection. Both the mobility and activity were reproducible for each molecule but differed between individual molecules. Assays were performed using uncoated capillaries and capillaries coated with different polymers, using enzymes from different sources and by three different experimental protocols. In all cases the observed ranges in electrophoretic mobilities were similar. The observed range in the electrophoretic mobility may be explained by structural microheterogeneity resulting in a gain or loss of up to 1.6 suppressed charge units. There was no observed relationship between the observed activities and electrophoretic mobilities. If the finding that individual beta-galactosidase molecules have heterogeneous electrophoretic mobility can be extended to other proteins, this may limit the resolution possible for capillary zone electrophoresis protein separations.
机译:大肠杆菌β-半乳糖苷酶单个分子的电泳迁移率和催化活性使用CE-LIF检测进行了测量。迁移率和活性对于每个分子都是可再现的,但是在单个分子之间是不同的。使用未涂覆的毛细管和涂覆有不同聚合物的毛细管,使用来自不同来源的酶并通过三种不同的实验方案进行测定。在所有情况下,观察到的电泳迁移率范围都相似。观察到的电泳迁移率范围可以用结构微异质性解释,该结构导致最多1.6个抑制电荷单元的得失。在观察到的活性和电泳迁移率之间没有观察到的关系。如果发现单个β-半乳糖苷酶分子具有不同的电泳迁移率的发现可以扩展到其他蛋白质,则这可能会限制毛细管区带电泳蛋白质分离的分辨率。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号