Suppr超能文献

单次毛细管区带电泳-质谱法可实现 27000 多种肽和近 4400 种蛋白质的鉴定,该方法结合了超低电渗流涂层毛细管、第三代电动鞘流纳米喷雾接口、轨道阱 Fusion Lumos Tribrid 质谱仪和高级峰检测算法。

Production of Over 27 000 Peptide and Nearly 4400 Protein Identifications by Single-Shot Capillary-Zone Electrophoresis-Mass Spectrometry via Combination of a Very-Low-Electroosmosis Coated Capillary, a Third-Generation Electrokinetically-Pumped Sheath-Flow Nanospray Interface, an Orbitrap Fusion Lumos Tribrid Mass Spectrometer, and an Advanced-Peak-Determination Algorithm.

机构信息

Department of Chemistry and Biochemistry , University of Notre Dame , Notre Dame , Indiana 46556 , United States.

Department of Biomolecular Chemistry, Genome Center of Wisconsin, and Department of Chemistry , University of Wisconsin , Madison , Wisconsin 53706 , United States.

出版信息

Anal Chem. 2018 Oct 16;90(20):12090-12093. doi: 10.1021/acs.analchem.8b02991. Epub 2018 Sep 24.

Abstract

We show that capillary-zone electrophoresis-electrospray ionization-tandem mass spectrometry (CZE-ESI-MS/MS) generates very large numbers of peptide and protein identifications (IDs) by combining four technologies: a separation capillary coated to generate very low electroosmosis, an electrokinetically pumped sheath-flow nanoelectrospray interface to produce high-sensitivity ionization, an Orbitrap Fusion Lumos Tribrid platform to provide high-speed analysis, and an advanced-peak-determination (APD) algorithm to take advantage of the mass spectrometer's data-acquisition speed. The use of the APD algorithm resulted in 2 times more identifications than the standard peak algorithm. We also investigated the effect of the isolation window, injection time, and loading amount. Optimization of these parameters produced over 27 000 peptide identifications and nearly 4400 protein-group identifications from 220 ng of K562-cell digest in a single 120 min run, which is 2.7 times more IDs produced by CZE-ESI-MS/MS than by the previous state-of-the-art technique.

摘要

我们展示了毛细管区带电泳-电喷雾串联质谱(CZE-ESI-MS/MS)通过结合四项技术产生了大量的肽和蛋白质鉴定(ID):一种涂覆的毛细管产生非常低的电渗流,一种电动泵鞘流纳喷雾接口产生高灵敏度的离子化,一种轨道阱 Fusion Lumos Tribrid 平台提供高速分析,以及一种高级峰检测(APD)算法利用质谱仪的数据采集速度。使用 APD 算法比标准峰算法产生的鉴定结果多 2 倍。我们还研究了隔离窗口、进样时间和加载量的影响。这些参数的优化从 220ng K562 细胞消化物中产生了超过 27000 种肽鉴定和近 4400 种蛋白质组鉴定,在单次 120 分钟运行中产生的 ID 比之前的最先进技术多 2.7 倍。

相似文献

引用本文的文献

7
Single-cell Proteomics: Progress and Prospects.单细胞蛋白质组学:进展与展望。
Mol Cell Proteomics. 2020 Nov;19(11):1739-1748. doi: 10.1074/mcp.R120.002234. Epub 2020 Aug 26.
9
Challenging Bioanalyses with Capillary Electrophoresis.毛细管电泳在具有挑战性的生物分析中的应用
Anal Chem. 2020 Jan 7;92(1):49-66. doi: 10.1021/acs.analchem.9b04718. Epub 2019 Dec 2.

本文引用的文献

3
Improved Precursor Characterization for Data-Dependent Mass Spectrometry.改进数据依赖型质谱分析的前体特征描述。
Anal Chem. 2018 Feb 6;90(3):2333-2340. doi: 10.1021/acs.analchem.7b04808. Epub 2018 Jan 11.

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