Suppr超能文献

基于简单集成的针尖技术应用于深度蛋白质组分析。

Simple and Integrated Spintip-Based Technology Applied for Deep Proteome Profiling.

机构信息

Department of Chemistry, Fudan University , Shanghai 200433, China.

ENT Institute of Shenzhen University, Shenzhen Longgang ENT Hospital , Shenzhen 518172, China.

出版信息

Anal Chem. 2016 May 3;88(9):4864-71. doi: 10.1021/acs.analchem.6b00631. Epub 2016 Apr 20.

Abstract

Great efforts have been taken for developing high-sensitive mass spectrometry (MS)-based proteomic technologies, among which sample preparation is one of the major focus. Here, a simple and integrated spintip-based proteomics technology (SISPROT) consisting of strong cation exchange beads and C18 disk in one pipet tip was developed. Both proteomics sample preparation steps, including protein preconcentration, reduction, alkylation, and digestion, and reversed phase (RP)-based desalting and high-pH RP-based peptide fractionation can be achieved in a fully integrated manner for the first time. This easy-to-use technology achieved high sensitivity with negligible sample loss. Proteomic analysis of 2000 HEK 293 cells readily identified 1270 proteins within 1.4 h of MS time, while 7826 proteins were identified when 100000 cells were processed and analyzed within only 22 h of MS time. More importantly, the SISPROT can be easily multiplexed on a standard centrifuge with good reproducibility (Pearson correlation coefficient > 0.98) for both single-shot analysis and deep proteome profiling with five-step high-pH RP fractionation. The SISPROT was exemplified by the triplicate analysis of 100000 stem cells from human exfoliated deciduous teeth (SHED). This led to the identification of 9078 proteins containing 3771 annotated membrane proteins, which was the largest proteome data set for dental stem cells reported to date. We expect that the SISPROT will be well suited for deep proteome profiling for fewer than 100000 cells and applied for translational studies where multiplexed technology with good label-free quantification precision is required.

摘要

已经付出了巨大努力来开发高灵敏度的基于质谱(MS)的蛋白质组学技术,其中样品制备是主要关注点之一。在这里,开发了一种简单而集成的基于自旋尖端的蛋白质组学技术(SISPROT),它由一个吸管尖端中的强阳离子交换珠和 C18 盘组成。首次可以完全集成地完成蛋白质组学样品制备步骤,包括蛋白质预浓缩、还原、烷基化和消化,以及基于反相(RP)的脱盐和基于高 pH 的 RP 肽分级。这种易于使用的技术实现了高灵敏度,几乎没有样品损失。对 2000 个 HEK 293 细胞的蛋白质组学分析在 1.4 小时的 MS 时间内轻松鉴定了 1270 种蛋白质,而当处理和分析 100000 个细胞时,仅在 22 小时的 MS 时间内就鉴定了 7826 种蛋白质。更重要的是,SISPROT 可以在标准离心机上轻松进行多重化,具有良好的重现性(Pearson 相关系数>0.98),可进行单次分析和深度蛋白质组分析,具有五步高 pH RP 分级。SISPROT 通过对来自人类脱落乳牙(SHED)的 100000 个干细胞的重复分析进行了说明。这导致鉴定了 9078 种蛋白质,其中包含 3771 种注释的膜蛋白,这是迄今为止报道的牙干细胞最大的蛋白质组数据集。我们预计 SISPROT 将非常适合少于 100000 个细胞的深度蛋白质组分析,并应用于需要具有良好无标记定量精度的多路复用技术的转化研究。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验