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Oxidized Form of Creatine Kinase

         

摘要

The purified rabbit muscle creatine kinase (R-CK) was previously considered homogeneousand without disulfide bonds.By the method of NR/R two-dimensional diagonal SDS-PAGE,two forms of R-CK,designated respectively "oxidized form" of creatine kinase which contained intrachain disulfide bondsand "reduced form" of creatine kinase which did not have any —S—S— bridges,were for the first time sepa-rated.They were found to be the same in amino acid composition,in subunit molecular Weight and in isoelec-tric point,and were almost identical in enzyme activities.Thus it is hard to isolate one from the other bycommon biochemical methods.More extensive studies show that the oxidized form of CK also contains a pair of reactive thiol groupswhich are essential to the enzyme activity,and it has one intrachain disulfide bond per subunit.In the nativestate,this —S—S— bond cannot be reduced by DTT,but by treating the reduced form of CK with some ox-idants,these —S—S— bonds can be formed in vitro.Thus it is presumed that the disulfide bonds are cross-linked through the oxidization of two shallowly buried —SH groups.

著录项

  • 来源
    《中国科学 》 |1994年第8期|964-974|共11页
  • 作者单位

    Department of Biological Science and Biotechnology;

    Tsinghua University;

    Beijing 100084;

    PRC;

    Permanent address:Integrated Program in CMBS;

    College of Physicians and Surgeons of Columbia University;

    New York;

    USA;

    Permanent address:Department of Biochemstry and Molecular Biophysics;

    Columbia University;

    New York;

    USA;

  • 原文格式 PDF
  • 正文语种 chi
  • 中图分类 R341;
  • 关键词

    creatine; klnase; oxidized; form; disulfide; bond; thiol; group;

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