Suppr超能文献

基于活性的探针在通过质谱流式细胞术数据采集确定细胞表面组织蛋白酶G的蛋白水解活性中的应用。

Application of an Activity-Based Probe to Determine Proteolytic Activity of Cell Surface Cathepsin G by Mass Cytometry Data Acquisition.

作者信息

Gärtner Fabian, Knippschild Uwe, Burster Timo

机构信息

Department of General and Visceral Surgery, Surgery Center, Ulm University Medical Center, 89081 Ulm, Germany.

Department of Biology, School of Sciences and Humanities, Nazarbayev University, Kabanbay Batyr Avenue, 53, Nur-Sultan 010000, Kazakhstan Republic.

出版信息

ACS Omega. 2020 Oct 19;5(43):28233-28238. doi: 10.1021/acsomega.0c04092. eCollection 2020 Nov 3.

Abstract

During an immune response, cathepsin G (CatG) takes on the role of adaptive and innate immunity and the outcome depends on the localization of CatG. Soluble, cell surface-bound, or intracellular CatG is also responsible for pathophysiology conditions. We applied the activity-based probe MARS116-Bt to mass cytometry by time-of-flight to analyze CatG activity on the cell surface of immune cells. The phosphonate warhead of MARS116-Bt binds covalently to the serine amino acid residue S195 of the catalytic center and thereby CatG activity can be detected. This method contributes to observing the activation or inhibition status of cells during pathogenesis of diseases and enables accurate data acquisition from complex biological samples with a vast panel of cell subset markers in a single-cell resolution.

摘要

在免疫反应过程中,组织蛋白酶G(CatG)兼具适应性免疫和先天性免疫的作用,其结果取决于CatG的定位。可溶性、细胞表面结合型或细胞内的CatG也与病理生理状况有关。我们将基于活性的探针MARS116-Bt应用于飞行时间质谱流式细胞术,以分析免疫细胞表面的CatG活性。MARS116-Bt的膦酸弹头与催化中心的丝氨酸氨基酸残基S195共价结合,从而能够检测CatG活性。该方法有助于观察疾病发病过程中细胞的激活或抑制状态,并能够以单细胞分辨率从具有大量细胞亚群标记物的复杂生物样本中准确获取数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fc8/7643251/46f09f5278a8/ao0c04092_0002.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验