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磷酸酶对富含亮氨酸重复激酶2(LRRK2)的调控

Regulation of LRRK2 by Phosphatases.

作者信息

Taymans Jean-Marc

机构信息

Université de Lille, Inserm, CHU Lille, UMR-S 1172-JPARC Jean-Pierre Aubert Research Center, Neurosciences and Cancer, 1 Place de Verdun, Lille, 59000, France.

出版信息

Adv Neurobiol. 2017;14:145-160. doi: 10.1007/978-3-319-49969-7_8.

Abstract

LRRK2 is a highly phosphorylated protein, and evidence of a physiological role for LRRK2 phosphorylation has accumulated in recent years for cellular phosphosites, many of which are found in the ANK-LRR interdomain region, i.e., the S910/S935/S955/S973 sites as well as recently for autophosphorylation sites, at least one of which has been confirmed in cells, S1292. LRRK2 phosphorylation is modulated in several disease or potential therapy relevant conditions such as in disease mutant variants of LRRK2 or following LRRK2 kinase inhibitor treatment. This chapter will focus on the regulation of LRRK2 phosphorylation and more specifically the role of phosphatases in LRRK2 dephosphorylation. This will include reviewing the conditions in which LRRK2 is found to be dephosphorylated, the molecular partners and phosphatases involved in regulating LRRK2 phosphorylation, as well as discussing how LRRK2 phosphatases may be therapeutic targets or biomarkers in their own right.

摘要

LRRK2是一种高度磷酸化的蛋白质,近年来,关于LRRK2磷酸化在细胞磷酸化位点的生理作用的证据不断积累,其中许多位点位于ANK-LRR结构域间区域,即S910/S935/S955/S973位点,以及最近发现的自磷酸化位点,其中至少有一个位点(S1292)已在细胞中得到证实。在几种与疾病或潜在治疗相关的情况下,如LRRK2的疾病突变变体或LRRK2激酶抑制剂治疗后,LRRK2的磷酸化会受到调节。本章将重点讨论LRRK2磷酸化的调节,更具体地说,是磷酸酶在LRRK2去磷酸化中的作用。这将包括回顾发现LRRK2去磷酸化的条件、参与调节LRRK2磷酸化的分子伴侣和磷酸酶,以及讨论LRRK2磷酸酶本身如何可能成为治疗靶点或生物标志物。

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