Development of Basic Proteomics Technology Using Monolithic Silica Columns and Its Application to Analysis of Pluripotent Stem Cells

DOI
  • Iwasaki Mio
    Kyoto University, Center for iPS Cell Research and Application

Bibliographic Information

Other Title
  • モノリスシリカカラムを用いたプロテオミクス基盤技術の開発と多能性幹細胞解析への展開

Abstract

<p>Current proteome analysis method is an effective method to comprehensively analyze the proteins, but it is still difficult to identify and quantify the proteins of a specific cell in a single analysis due to the complexity of the proteome samples. We have been working on the development of basic technologies to solve this problem and improve the identification and quantification efficiency. We have focused on the use of monolithic columns to improve separation efficiency and have developed the RiMS (removal of interference mixture spectra) method, which improves the accuracy of isobaric labelling quantification. We applied this method to the analysis of pluripotent stem cells, resulting improved quantification accuracy of cell type-specific proteins. In this paper, we will introduce the RiMS method with an overview of the methods used for quantitative proteome analysis.</p>

Journal

  • Proteome Letters

    Proteome Letters 6 (2), 61-68, 2021

    Japanese Proteomics Society

Details 詳細情報について

  • CRID
    1390572244931745792
  • NII Article ID
    130008140152
  • DOI
    10.14889/jpros.6.2_61
  • ISSN
    24322776
  • Text Lang
    ja
  • Data Source
    • JaLC
    • CiNii Articles
  • Abstract License Flag
    Disallowed

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