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Development of INSOL-tag for proteome-wide protein handling and its application in protein array analysis.
Fukuda, Eriko; Mori, Masatoshi; Shiku, Hiroshi; Miyahara, Yoshihiro; Kawamura, Yoshifumi; Ogawa, Koji; Ogura, Toshihiko; Goshima, Naoki.
Afiliação
  • Fukuda E; Molecular Profiling Research Center for Drug Discovery, National Institute of Advanced Industrial Science and Technology, Koto-ku, Tokyo, Japan.
  • Mori M; Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki, Japan.
  • Shiku H; Molecular Profiling Research Center for Drug Discovery, National Institute of Advanced Industrial Science and Technology, Koto-ku, Tokyo, Japan.
  • Miyahara Y; Department of Immuno-Gene Therapy, Mie University Graduate School of Medicine, Tsu, Mie, Japan.
  • Kawamura Y; Department of Immuno-Gene Therapy, Mie University Graduate School of Medicine, Tsu, Mie, Japan.
  • Ogawa K; Japan Biological Informatics Consortium, Koto-ku, Tokyo, Japan.
  • Ogura T; Molecular Profiling Research Center for Drug Discovery, National Institute of Advanced Industrial Science and Technology, Koto-ku, Tokyo, Japan.
  • Goshima N; Biomedical Research Institute, National Institute of Advanced Industrial Science and Technology, Tsukuba, Ibaraki, Japan.
Genes Cells ; 25(1): 41-53, 2020 Jan.
Article em En | MEDLINE | ID: mdl-31733161
Proteomic analysis requires protein tags that enable high-throughput handling; however, versatile tags that can be used in in vitro expression systems are currently lacking. In this study, we developed an insoluble protein tag, INSOL-tag, derived from human transcription factor MafG. The INSOL-tagged target protein is expressed in a eukaryotic in vitro expression system and recovered as a pellet following centrifugation at 19,000 × g for 20 min. Comparisons of the target protein recovery rates of GST-tag and INSOL-tag using 111 cytoplasmic proteins revealed a fourfold increase in the yield of INSOL-tagged proteins. Using 267 cancer antigens purified with INSOL-tag, we subsequently developed an INSOL-CTA array method, for profiling autoantibodies in sera of cancer patients. The detection limit of the array was approximately 11.1 pg IgG, and the correlation with ELISA was high (R2  = .993, .955). Moreover, when autoantibody profiling of digestive cancer patient sera was performed, antigen spreading was observed. These data suggest that INSOL-tag is a versatile tag that can insolubilize a wide range of target proteins. It is therefore expected to become a powerful tool in comprehensive protein preparation for protein arrays, antibody production, and mass spectrometry.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Repressoras / Proteômica / Fator de Transcrição MafG Limite: Humans Idioma: En Revista: Genes Cells Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Japão País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Repressoras / Proteômica / Fator de Transcrição MafG Limite: Humans Idioma: En Revista: Genes Cells Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Japão País de publicação: Reino Unido