{"title":"Quantification of Cellular Proteostasis in Live Cells by Fluorogenic Assay Using the AgHalo Sensor","authors":"Matthew Fares, Xin Zhang","doi":"10.1002/cpch.58","DOIUrl":null,"url":null,"abstract":"<p>Proper cellular proteostasis is essential to cellular fitness and viability. Exogenous stress conditions compromise proteostasis and cause aggregation of cellular proteins. We have developed a fluorogenic sensor (AgHalo) to quantify stress-induced proteostasis deficiency. The AgHalo sensor uses a destabilized HaloTag variant to represent aggregation-prone cellular proteins and is equipped with a series of fluorogenic probes that exhibit a fluorescence increase when the sensor forms either soluble oligomers or insoluble aggregates. Herein, we present protocols that describe how the AgHalo sensor can be employed to visualize and quantify proteome stress in live cells using a direct fluorescence read-out and visualization with a fluorescence microplate reader and a microscope. Additionally, protocols for using the AgHalo sensor in combination with fluorogenic probes and commercially available HaloTag probes to enable two-color imaging experiments are described. These protocols will enable use of the AgHalo sensor to visualize and quantify proteostasis in live cells, a task that is difficult to accomplish using previous, always-fluorescent methods. © 2018 by John Wiley & Sons, Inc.</p>","PeriodicalId":38051,"journal":{"name":"Current protocols in chemical biology","volume":"11 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpch.58","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current protocols in chemical biology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpch.58","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 1
Abstract
Proper cellular proteostasis is essential to cellular fitness and viability. Exogenous stress conditions compromise proteostasis and cause aggregation of cellular proteins. We have developed a fluorogenic sensor (AgHalo) to quantify stress-induced proteostasis deficiency. The AgHalo sensor uses a destabilized HaloTag variant to represent aggregation-prone cellular proteins and is equipped with a series of fluorogenic probes that exhibit a fluorescence increase when the sensor forms either soluble oligomers or insoluble aggregates. Herein, we present protocols that describe how the AgHalo sensor can be employed to visualize and quantify proteome stress in live cells using a direct fluorescence read-out and visualization with a fluorescence microplate reader and a microscope. Additionally, protocols for using the AgHalo sensor in combination with fluorogenic probes and commercially available HaloTag probes to enable two-color imaging experiments are described. These protocols will enable use of the AgHalo sensor to visualize and quantify proteostasis in live cells, a task that is difficult to accomplish using previous, always-fluorescent methods. © 2018 by John Wiley & Sons, Inc.
用AgHalo传感器荧光测定活细胞中细胞蛋白酶的含量
适当的细胞蛋白酶抑制对细胞的健康和活力至关重要。外源应激条件损害蛋白质平衡并引起细胞蛋白质聚集。我们开发了一种荧光传感器(AgHalo)来量化应力诱导的蛋白酶抑制缺陷。AgHalo传感器使用不稳定的HaloTag变体来表示易于聚集的细胞蛋白,并配备了一系列荧光探针,当传感器形成可溶性低聚物或不可溶性聚集体时,荧光会增加。在此,我们提出了描述AgHalo传感器如何使用直接荧光读出和荧光微孔板读取器和显微镜可视化来可视化和量化活细胞中的蛋白质组应激的方案。此外,还描述了将AgHalo传感器与荧光探针和市售HaloTag探针结合使用以实现双色成像实验的协议。这些协议将使AgHalo传感器能够可视化和量化活细胞中的蛋白质静止,这是使用以前的荧光方法难以完成的任务。©2018 by John Wiley &儿子,Inc。
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