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本文引用的文献

1
Strong cation exchange-reversed phase liquid chromatography-capillary zone electrophoresis-tandem mass spectrometry platform with high peak capacity for deep bottom-up proteomics.用于深度从头蛋白质组学的高峰容量强阳离子交换反相液相色谱-毛细管区带电泳-串联质谱平台。
Anal Chim Acta. 2018 Jul 5;1012:1-9. doi: 10.1016/j.aca.2018.01.037. Epub 2018 Feb 5.
2
Optimization of mass spectrometric parameters improve the identification performance of capillary zone electrophoresis for single-shot bottom-up proteomics analysis.优化质谱参数可提高毛细管区带电泳在单次从头蛋白质组分析中的鉴定性能。
Anal Chim Acta. 2018 Feb 25;1001:93-99. doi: 10.1016/j.aca.2017.11.023. Epub 2017 Nov 14.
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.
4
Enhancing Proteomic Throughput in Capillary Electrophoresis-Mass Spectrometry by Sequential Sample Injection.通过连续进样提高毛细管电泳-质谱联用中的蛋白质组学通量
Proteomics. 2017 Nov;17(22). doi: 10.1002/pmic.201700310. Epub 2017 Oct 25.
5
Multisegment injections improve peptide identification rates in capillary zone electrophoresis-based bottom-up proteomics.多段注射提高了基于毛细管区带电泳的自下而上蛋白质组学中的肽段鉴定率。
J Chromatogr A. 2017 Nov 10;1523:123-126. doi: 10.1016/j.chroma.2017.07.022. Epub 2017 Jul 8.
6
Surface-Confined Aqueous Reversible Addition-Fragmentation Chain Transfer (SCARAFT) Polymerization Method for Preparation of Coated Capillary Leads to over 10 000 Peptides Identified from 25 ng HeLa Digest by Using Capillary Zone Electrophoresis-Tandem Mass Spectrometry.基于表面受限的可逆加成-断裂链转移(SCARAFT)聚合方法制备涂层毛细管,用于毛细管区带电泳-串联质谱法从 25ng HeLa 酶解物中鉴定出超过 10000 种肽段。
Anal Chem. 2017 Jun 20;89(12):6774-6780. doi: 10.1021/acs.analchem.7b01147. Epub 2017 Jun 7.
7
Predicting Electrophoretic Mobility of Tryptic Peptides for High-Throughput CZE-MS Analysis.预测酶解肽段的电泳淌度用于高通量 CZE-MS 分析。
Anal Chem. 2017 Feb 7;89(3):2000-2008. doi: 10.1021/acs.analchem.6b04544. Epub 2017 Jan 19.
8
Now, More Than Ever, Proteomics Needs Better Chromatography.当下,蛋白质组学比以往任何时候都更需要更好的色谱技术。
Cell Syst. 2016 Oct 26;3(4):321-324. doi: 10.1016/j.cels.2016.10.007.
9
Single-Cell Mass Spectrometry for Discovery Proteomics: Quantifying Translational Cell Heterogeneity in the 16-Cell Frog (Xenopus) Embryo.用于发现蛋白质组学的单细胞质谱分析:量化16细胞期非洲爪蟾胚胎中的翻译细胞异质性
Angew Chem Int Ed Engl. 2016 Feb 12;55(7):2454-8. doi: 10.1002/anie.201510411. Epub 2016 Jan 12.
10
Nearly 1000 Protein Identifications from 50 ng of Xenopus laevis Zygote Homogenate Using Online Sample Preparation on a Strong Cation Exchange Monolith Based Microreactor Coupled with Capillary Zone Electrophoresis.使用基于强阳离子交换整体柱的微反应器在线样品制备结合毛细管区带电泳,从50纳克非洲爪蟾受精卵匀浆中鉴定出近1000种蛋白质。
Anal Chem. 2016 Jan 5;88(1):877-82. doi: 10.1021/acs.analchem.5b03496. Epub 2015 Dec 15.

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.

DOI:10.1021/acs.analchem.8b02991
PMID:30179504
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6508074/
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。