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PARPs 和 ADP-ribosylation 对炎症和宿主-病原体相互作用的影响。

The impact of PARPs and ADP-ribosylation on inflammation and host-pathogen interactions.

机构信息

Department of Molecular Biosciences, University of Kansas, Lawrence, Kansas 66045, USA.

Center for Interdisciplinary Cardiovascular Sciences, Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Genes Dev. 2020 Mar 1;34(5-6):341-359. doi: 10.1101/gad.334425.119. Epub 2020 Feb 6.

Abstract

Poly-adenosine diphosphate-ribose polymerases (PARPs) promote ADP-ribosylation, a highly conserved, fundamental posttranslational modification (PTM). PARP catalytic domains transfer the ADP-ribose moiety from NAD to amino acid residues of target proteins, leading to mono- or poly-ADP-ribosylation (MARylation or PARylation). This PTM regulates various key biological and pathological processes. In this review, we focus on the roles of the PARP family members in inflammation and host-pathogen interactions. Here we give an overview the current understanding of the mechanisms by which PARPs promote or suppress proinflammatory activation of macrophages, and various roles PARPs play in virus infections. We also demonstrate how innovative technologies, such as proteomics and systems biology, help to advance this research field and describe unanswered questions.

摘要

聚腺苷二磷酸核糖聚合酶 (PARPs) 促进 ADP-核糖基化,这是一种高度保守的基本翻译后修饰 (PTM)。PARP 催化结构域将 ADP-核糖部分从 NAD 转移到靶蛋白的氨基酸残基上,导致单或多 ADP-核糖基化 (MARylation 或 PARylation)。这种 PTM 调节各种关键的生物学和病理学过程。在这篇综述中,我们重点介绍 PARP 家族成员在炎症和宿主-病原体相互作用中的作用。在这里,我们概述了 PARPs 促进或抑制巨噬细胞促炎激活的机制,以及 PARPs 在病毒感染中发挥的各种作用。我们还展示了蛋白质组学和系统生物学等创新技术如何帮助推进这一研究领域,并描述了未解决的问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc3d/7050484/f460e05c3f9b/341f01.jpg

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