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对辅因子作为糖原磷酸化酶周转标记物的进一步评估。

Further evaluation of cofactor as a turnover label for glycogen phosphorylase.

作者信息

Cookson E J, Beynon R J

机构信息

Department of Biochemistry, University of Liverpool, England.

出版信息

Int J Biochem. 1989;21(9):975-82. doi: 10.1016/0020-711x(89)90229-2.

Abstract
  1. The cofactor of glycogen phosphorylase, pyridoxal phosphate (PLP), is stably associated with the enzyme and has been used as a label in the determination of the turnover of the skeletal muscle enzyme in vivo. 2. Mice were injected with radiolabelled pyridoxine that was subsequently converted to PLP and incorporated into phosphorylase. 3. In this study we have resolved phosphorylase-bound label from that associated with the other PLP-containing enzymes and free label by affinity and size-exclusion chromatography. 4. The decay of radioactive pools was assessed after an extended period post-injection to minimize the effects of isotope reutilization. 5. These modifications have allowed refinement of our previous estimate of the rate of degradation of muscle phosphorylase.
摘要
  1. 糖原磷酸化酶的辅因子磷酸吡哆醛(PLP)与该酶稳定结合,并已被用作体内测定骨骼肌酶周转率的标记物。2. 给小鼠注射放射性标记的吡哆醇,其随后转化为PLP并掺入磷酸化酶中。3. 在本研究中,我们通过亲和色谱和尺寸排阻色谱法,将与磷酸化酶结合的标记物与其他含PLP的酶相关的标记物及游离标记物区分开来。4. 在注射后延长一段时间后评估放射性池的衰减,以尽量减少同位素再利用的影响。5. 这些改进使我们能够对之前关于肌肉磷酸化酶降解速率的估计进行优化。

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