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用于检测近端磷酸化肽和蛋白质的光学化学传感器。

Optical chemosensors for the detection of proximally phosphorylated peptides and proteins.

作者信息

Cabral Aaron D, Radu Tudor B, de Araujo Elvin D, Gunning Patrick T

机构信息

Department of Chemical and Physical Sciences, University of Toronto Mississauga 3359 Mississauga Road Mississauga Ontario L5L 1C6 Canada

Department of Chemistry, University of Toronto 80 St George Street Toronto Ontario M5S 3H6 Canada.

出版信息

RSC Chem Biol. 2021 Apr 21;2(3):815-829. doi: 10.1039/d1cb00055a. eCollection 2021 Jun 1.

Abstract

Proximal multi-site phosphorylation is a critical post-translational modification in protein biology. The additive effects of multiple phosphosite clusters in close spatial proximity triggers integrative and cooperative effects on protein conformation and activity. Proximal phosphorylation has been shown to modulate signal transduction pathways and gene expression, and as a result, is implicated in a broad range of disease states through altered protein function and/or localization including enzyme overactivation or protein aggregation. The role of proximal multi-phosphorylation events is becoming increasingly recognized as mechanistically important, although breakthroughs are limited due to a lack of detection technologies. To date, there is a limited selection of facile and robust sensing tools for proximal phosphorylation. Nonetheless, there have been considerable efforts in developing optical chemosensors for the detection of proximal phosphorylation motifs on peptides and proteins in recent years. This review provides a comprehensive overview of optical chemosensors for proximal phosphorylation, with the majority of work being reported in the past two decades. Optical sensors, in the form of fluorescent and luminescent chemosensors, hybrid biosensors, and inorganic nanoparticles, are described. Emphasis is placed on the rationale behind sensor scaffolds, relevant protein motifs, and applications in protein biology.

摘要

近端多位点磷酸化是蛋白质生物学中一种关键的翻译后修饰。紧密空间邻近的多个磷酸化位点簇的累加效应触发了对蛋白质构象和活性的整合与协同作用。近端磷酸化已被证明可调节信号转导通路和基因表达,因此,通过改变蛋白质功能和/或定位,包括酶过度激活或蛋白质聚集,它与多种疾病状态有关。尽管由于缺乏检测技术,突破有限,但近端多磷酸化事件的作用在机制上的重要性正日益得到认可。迄今为止,用于近端磷酸化的简便且强大的传感工具选择有限。尽管如此,近年来在开发用于检测肽和蛋白质上近端磷酸化基序的光学化学传感器方面已经做出了相当大的努力。本综述全面概述了用于近端磷酸化的光学化学传感器,大部分工作是在过去二十年中报道的。文中描述了以荧光和发光化学传感器、混合生物传感器及无机纳米颗粒形式存在的光学传感器。重点在于传感器支架背后的原理、相关蛋白质基序以及在蛋白质生物学中的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04f7/8341930/41392ef3256c/d1cb00055a-f1.jpg

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