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重组大鼠和人多聚(ADP-核糖)聚合酶-1 的酶学特性反映了细胞多聚(ADP-核糖)化能力与种属特异性寿命之间的相关性。

Enzyme characteristics of recombinant poly(ADP-ribose) polymerases-1 of rat and human origin mirror the correlation between cellular poly(ADP-ribosyl)ation capacity and species-specific life span.

机构信息

Molecular Toxicology Group, Department of Biology, University of Konstanz, Universitaetsstr. 10, 78457 Konstanz, Germany.

出版信息

Mech Ageing Dev. 2010 May;131(5):366-9. doi: 10.1016/j.mad.2010.04.003. Epub 2010 Apr 24.

Abstract

Poly(ADP-ribosyl)ation is a posttranslational modification, which is involved in many cellular functions, including DNA repair and maintenance of genomic stability, and has also been implicated in cellular and organismal ageing. We have previously reported that maximum poly(ADP-ribosyl)ation capacity in mononuclear blood cells is correlated with mammalian life span. Here we show that the difference between a long-lived and a short-lived species tested (i.e. man and rat) is directly mirrored by the enzymatic parameters of recombinant poly(ADP-ribose) polymerase-1 (PARP-1), i.e. substrate affinity and reaction velocity. In addition, we have characterized two human PARP-1 alleles and assign their activity difference to their respective initial velocity and not substrate affinity.

摘要

聚(ADP-核糖)化是一种翻译后修饰,涉及许多细胞功能,包括 DNA 修复和基因组稳定性的维持,也与细胞和机体衰老有关。我们之前报道过,单核血细胞中的最大聚(ADP-核糖)化能力与哺乳动物的寿命有关。在这里,我们表明,在经过测试的长寿命和短寿命物种(即人和大鼠)之间的差异,直接反映在重组聚(ADP-核糖)聚合酶-1(PARP-1)的酶学参数上,即底物亲和力和反应速度。此外,我们还对两种人类 PARP-1 等位基因进行了表征,并将其活性差异归因于各自的初始速度,而不是底物亲和力。

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