Literature DB >> 24666247

Hydrophilic interaction chromatography using a meter-scale monolithic silica capillary column for proteomics LC-MS.

Kanta Horie1, Takeo Kamakura, Tohru Ikegami, Masaki Wakabayashi, Takashi Kato, Nobuo Tanaka, Yasushi Ishihama.   

Abstract

A meter-scale monolithic silica capillary column modified with urea-functional groups for hydrophilic interaction liquid chromatography (HILIC) was developed for highly efficient separation of biological compounds. We prepared a ureidopropylsilylated monolithic silica capillary column with a minimum plate height of 12 μm for nucleosides and a permeability of 2.1 × 10(-13) m(2), which is comparable with the parameters of monolithic silica-C18 capillary columns. Over 300,000 theoretical plates were experimentally obtained in HILIC with a 4 m long column at 8 MPa; this is the best result yet reported for HILIC. A 2 m long ureidopropylsilylated monolithic silica capillary column was utilized to develop a HILIC mode LC-MS system for proteomics applications. Using tryptic peptides from human HeLa cell lysate proteins, we identified the comparable numbers of peptides and proteins in HILIC with those in reversed-phase liquid chromatography (RPLC) using a C18-modified monolithic silica column when shallow gradients were applied. In addition, approximately 5-fold increase in the peak response on average was observed in HILIC for commonly identified tryptic peptides due to the high acetonitrile concentration in the HILIC mobile phase. Since HILIC mode LC-MS shows orthogonal selectivity to RPLC mode LC-MS, it is useful as a complementary tool to increase proteome coverage in proteomics studies.

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Year:  2014        PMID: 24666247     DOI: 10.1021/ac4038625

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  7 in total

1.  Detachable strong cation exchange monolith, integrated with capillary zone electrophoresis and coupled with pH gradient elution, produces improved sensitivity and numbers of peptide identifications during bottom-up analysis of complex proteomes.

Authors:  Zhenbin Zhang; Xiaojing Yan; Liangliang Sun; Guijie Zhu; Norman J Dovichi
Journal:  Anal Chem       Date:  2015-04-10       Impact factor: 6.986

Review 2.  Nano-liquid chromatography-mass spectrometry and recent applications in omics investigations.

Authors:  Katherine L Sanders; James L Edwards
Journal:  Anal Methods       Date:  2020-09-09       Impact factor: 2.896

3.  Now, More Than Ever, Proteomics Needs Better Chromatography.

Authors:  Evgenia Shishkova; Alexander S Hebert; Joshua J Coon
Journal:  Cell Syst       Date:  2016-10-26       Impact factor: 10.304

Review 4.  Advances in microscale separations towards nanoproteomics applications.

Authors:  Lian Yi; Paul D Piehowski; Tujin Shi; Richard D Smith; Wei-Jun Qian
Journal:  J Chromatogr A       Date:  2017-07-21       Impact factor: 4.759

5.  Evaluating the use of HILIC in large-scale, multi dimensional proteomics: Horses for courses?

Authors:  Dalila Bensaddek; Armel Nicolas; Angus I Lamond
Journal:  Int J Mass Spectrom       Date:  2015-11-30       Impact factor: 1.986

Review 6.  MS1 ion current-based quantitative proteomics: A promising solution for reliable analysis of large biological cohorts.

Authors:  Xue Wang; Shichen Shen; Sailee Suryakant Rasam; Jun Qu
Journal:  Mass Spectrom Rev       Date:  2019-03-28       Impact factor: 10.946

7.  Single-Shot 10K Proteome Approach: Over 10,000 Protein Identifications by Data-Independent Acquisition-Based Single-Shot Proteomics with Ion Mobility Spectrometry.

Authors:  Yusuke Kawashima; Hirotaka Nagai; Ryo Konno; Masaki Ishikawa; Daisuke Nakajima; Hironori Sato; Ren Nakamura; Tomoyuki Furuyashiki; Osamu Ohara
Journal:  J Proteome Res       Date:  2022-05-06       Impact factor: 5.370

  7 in total

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