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一份基于质谱分析得出的细胞表面蛋白质图谱。

A mass spectrometric-derived cell surface protein atlas.

作者信息

Bausch-Fluck Damaris, Hofmann Andreas, Bock Thomas, Frei Andreas P, Cerciello Ferdinando, Jacobs Andrea, Moest Hansjoerg, Omasits Ulrich, Gundry Rebekah L, Yoon Charles, Schiess Ralph, Schmidt Alexander, Mirkowska Paulina, Härtlová Anetta, Van Eyk Jennifer E, Bourquin Jean-Pierre, Aebersold Ruedi, Boheler Kenneth R, Zandstra Peter, Wollscheid Bernd

机构信息

Institute of Molecular Systems Biology, ETH Zurich, Zurich, Switzerland; Department of Health Sciences and Technology, BMPP, ETH Zurich, Zurich, Switzerland.

Institute of Molecular Systems Biology, ETH Zurich, Zurich, Switzerland.

出版信息

PLoS One. 2015 Apr 20;10(3):e0121314. doi: 10.1371/journal.pone.0121314. eCollection 2015.

Abstract

Cell surface proteins are major targets of biomedical research due to their utility as cellular markers and their extracellular accessibility for pharmacological intervention. However, information about the cell surface protein repertoire (the surfaceome) of individual cells is only sparsely available. Here, we applied the Cell Surface Capture (CSC) technology to 41 human and 31 mouse cell types to generate a mass-spectrometry derived Cell Surface Protein Atlas (CSPA) providing cellular surfaceome snapshots at high resolution. The CSPA is presented in form of an easy-to-navigate interactive database, a downloadable data matrix and with tools for targeted surfaceome rediscovery (http://wlab.ethz.ch/cspa). The cellular surfaceome snapshots of different cell types, including cancer cells, resulted in a combined dataset of 1492 human and 1296 mouse cell surface glycoproteins, providing experimental evidence for their cell surface expression on different cell types, including 136 G-protein coupled receptors and 75 membrane receptor tyrosine-protein kinases. Integrated analysis of the CSPA reveals that the concerted biological function of individual cell types is mainly guided by quantitative rather than qualitative surfaceome differences. The CSPA will be useful for the evaluation of drug targets, for the improved classification of cell types and for a better understanding of the surfaceome and its concerted biological functions in complex signaling microenvironments.

摘要

细胞表面蛋白是生物医学研究的主要靶点,因为它们可作为细胞标志物,并且其细胞外区域可用于药物干预。然而,关于单个细胞的细胞表面蛋白库(表面组)的信息却十分稀少。在此,我们将细胞表面捕获(CSC)技术应用于41种人类细胞类型和31种小鼠细胞类型,以生成一个基于质谱的细胞表面蛋白图谱(CSPA),从而提供高分辨率的细胞表面组快照。CSPA以易于浏览的交互式数据库、可下载的数据矩阵以及用于靶向表面组重新发现的工具(http://wlab.ethz.ch/cspa)的形式呈现。不同细胞类型(包括癌细胞)的细胞表面组快照产生了一个包含1492种人类细胞表面糖蛋白和1296种小鼠细胞表面糖蛋白的综合数据集,为它们在不同细胞类型上的细胞表面表达提供了实验证据,其中包括136种G蛋白偶联受体和75种膜受体酪氨酸蛋白激酶。对CSPA的综合分析表明,单个细胞类型的协同生物学功能主要由表面组的定量差异而非定性差异所引导。CSPA将有助于评估药物靶点、改进细胞类型分类以及更好地理解复杂信号微环境中的表面组及其协同生物学功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d9f/4404347/ac9479792a65/pone.0121314.g001.jpg

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