Kharitidi Dmitri, Manteghi Sanaz, Pause Arnim
Department of Biochemistry and Goodman Cancer Research Centre, McGill University, 3655, Promenade Sir William Osler, Montreal, QC H3G 1Y6, Canada.
Methods. 2014 Jan 15;65(2):207-18. doi: 10.1016/j.ymeth.2013.09.009. Epub 2013 Sep 21.
Protein tyrosine phosphatases (PTPs) are key enzymes in the regulation of cellular homeostasis and signaling pathways. Strikingly, not all PTPs bear enzymatic activity. A considerable fraction of PTPs are enzymatically inactive and are known as pseudophosphatases. Despite the lack of activity they execute pivotal roles in development, cell biology and human disease. The present review is focused on the methods used to identify pseudophosphatases, their targets, and physiological roles. We present a strategy for detailed enzymatic analysis of inactive PTPs, regulation of inactive PTP domains and identification of binding partners. Furthermore, we provide a detailed overview of human pseudophosphatases and discuss their regulation of cellular processes and functions in human pathologies.
蛋白酪氨酸磷酸酶(PTPs)是调节细胞内稳态和信号通路的关键酶。值得注意的是,并非所有PTPs都具有酶活性。相当一部分PTPs在酶学上是无活性的,被称为假磷酸酶。尽管缺乏活性,但它们在发育、细胞生物学和人类疾病中发挥着关键作用。本综述重点关注用于鉴定假磷酸酶、其靶点和生理作用的方法。我们提出了一种对无活性PTPs进行详细酶学分析、调节无活性PTP结构域以及鉴定结合伴侣的策略。此外,我们详细概述了人类假磷酸酶,并讨论了它们在人类病理学中对细胞过程和功能的调节。