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肌酸激酶同工酶(EC 2.7.3.2)的合成后变化

Post-synthetic changes in creatine kinase isozymes (EC 2.7.3.2).

作者信息

Wevers R A, Delsing M, Klein Gebbink J A, Soons J B

出版信息

Clin Chim Acta. 1978 Jun 15;86(3):323-7. doi: 10.1016/0009-8981(78)90388-1.

Abstract
  1. An in vivo change from creatine kinase MM3 into MM2 and finally into MM1 was described earlier in sera of patients during a post-myocardial infarction period. The same change takes place in vitro. 2. Parallel to this change, a turn-over from the MB2 isozyme into the MB1 form can be detected in vitro. 3. Immediately after the mixing of various extracts from heart tissue and other muscles with a serum with low creatine kinase activity, only MM3 and MB2 can be detected. MM1, MM2 and MB1 are not present in muscle cells. From these three observations it can be concluded that the phenomenon of the three MM and two MB isozymes is postsynthetic (i.e. epigenetic). Furthermore evidence is presented that the change from MM3 into MM1 is brought about by a thermolabile substance. This factor transforms one of the two M2 chains, present in the MM3 form, into a M1 chain. This results in the MM2 isozyme. Later on the second M2 chain is also transformed, resulting in the MM1 isozyme. The same mechanism is proposed for the observed change in MB pattern.
摘要
  1. 早期研究表明,在心肌梗死后的一段时间内,患者血清中肌酸激酶MM3会转变为MM2,最终转变为MM1。体外也会发生同样的变化。2. 与此变化平行的是,体外可检测到MB2同工酶向MB1形式的转变。3. 将心脏组织和其他肌肉的各种提取物与肌酸激酶活性低的血清混合后,立即只能检测到MM3和MB2。MM1、MM2和MB1不存在于肌肉细胞中。从这三个观察结果可以得出结论,三种MM和两种MB同工酶的现象是合成后(即表观遗传)的。此外,有证据表明,从MM3转变为MM1是由一种热不稳定物质引起的。该因子将MM3形式中存在的两条M2链之一转化为M1链。这就产生了MM2同工酶。随后第二条M2链也发生转化,产生MM1同工酶。对于观察到的MB模式变化,也提出了相同的机制。

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