Mixed Alkyl Aryl Phosphonates as Quenched Activity-Based Probes for Real-Time Imaging of Active Neutrophil Serine Proteases

IF 3.8 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Jan Pascal Kahler, , , Jonathan Coene, , , Marcin Skorenski, , , Dimitris Korovesis, , and , Steven H. L. Verhelst*, 
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引用次数: 0

Abstract

Activity-based probes have been instrumental in the study of proteases, and quenched fluorescent versions can be utilized in real time imaging. Unfortunately, this application has not yet been reported for serine proteases, which make up the largest mechanistic class of proteases. Here, we describe quenched activity-based probes for detection of serine proteases, specifically the neutrophil serine proteases: neutrophil elastase, proteinase 3, and cathepsin G. We demonstrate that these reagents can selectively label serine proteases in complex proteomes and we illustrate their use in the live cell imaging of activation of primary human neutrophils. We expect that these reagents will find use in real-time imaging of active neutrophil serine proteases and may be further developed for imaging of other serine proteases.

Abstract Image

混合烷基芳基膦酸盐作为活性中性粒细胞丝氨酸蛋白酶实时成像的猝灭活性探针。
基于活性的探针已经在蛋白酶的研究中发挥了重要作用,并且淬灭的荧光版本可以用于实时成像。不幸的是,这种应用尚未报道丝氨酸蛋白酶,这是最大的机制类蛋白酶。在这里,我们描述了用于检测丝氨酸蛋白酶的猝灭活性探针,特别是中性粒细胞丝氨酸蛋白酶:中性粒细胞弹性蛋白酶、蛋白酶3和组织蛋白酶g。我们证明了这些试剂可以选择性地标记复杂蛋白质组中的丝氨酸蛋白酶,并说明了它们在原代人中性粒细胞活化的活细胞成像中的应用。我们期望这些试剂将用于活性中性粒细胞丝氨酸蛋白酶的实时成像,并可能进一步开发用于其他丝氨酸蛋白酶的成像。
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来源期刊
ACS Chemical Biology
ACS Chemical Biology 生物-生化与分子生物学
CiteScore
7.50
自引率
5.00%
发文量
353
审稿时长
3.3 months
期刊介绍: ACS Chemical Biology provides an international forum for the rapid communication of research that broadly embraces the interface between chemistry and biology. The journal also serves as a forum to facilitate the communication between biologists and chemists that will translate into new research opportunities and discoveries. Results will be published in which molecular reasoning has been used to probe questions through in vitro investigations, cell biological methods, or organismic studies. We welcome mechanistic studies on proteins, nucleic acids, sugars, lipids, and nonbiological polymers. The journal serves a large scientific community, exploring cellular function from both chemical and biological perspectives. It is understood that submitted work is based upon original results and has not been published previously.
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