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Role of PARP and protein poly-ADP-ribosylation process in regulation of cell functions

机译:PARP和蛋白质聚-ADP-核糖基化方法在细胞功能调节中的作用

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This review focuses on the biological role of enzymes involved in posttranslational modification of proteins by their poly-ADP-ribosylation, a NAD-consuming process with an emerging key role in providing fundamental cell functions. To this end, detailed analysis of structural organization in relation to basic functions of the poly(ADP-ribose)polymerase-1 (PARP-1), the founding member of the PARP family, and other poly(ADP-ribose)polymerase isoforms is presented here. These include the current views on the role of PARP family enzymes and processes of poly-ADP-ribosylation of proteins in chromatin structure remodeling, DNA damage repair, regulation of gene expression, and integration of cellular signaling pathways. Considerable attention is paid to the involvement of PARP in cellular functions, particularly in cell division, intracellular transport of macromolcules, proteasomal protein degradation, immune response and caspase-independent necrotic pathways defined as necroptosis (programmed necrosis). In the light of the remarkable successes that have been reported for treating inflammatory disorders and cancer with different classes of PARPs inhibitors, we discuss the prospects of targeting PARPs with therapeutic purposes.
机译:本综述重点介绍酶参与蛋白质的酶改性的酶的生物学作用,其具有新出现的方法在提供基本细胞功能方面具有新出现的关键作用。为此,对与聚(ADP-核糖)聚合酶-1(PARP-1)的基本功能有关的结构组织的详细分析,PARP家族的创始构件和其他聚(ADP-核糖)聚合酶同种型是在这里提出。这些包括关于PARP家族酶的作用的目前的观点和染色质结构重塑,DNA损伤修复,基因表达调节的DNA损伤修复,调节和细胞信号通路的整合。对PARP在细胞功能中的累积中,特别是在细胞分裂,大分子细胞分泌,蛋白质蛋白质降解,免疫应答和患者无关的坏死途径中被定义为Necroptis(编程坏死)的细胞分裂。鉴于治疗具有不同类别的PARPS抑制剂的炎性疾病和癌症的显着成功,我们讨论了靶向PARP的前景。

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