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ESTABLISHMENT OF A NEW METHOD FOR PROTEIN ANALYSIS AFTER CULTURING CELLS ON PROTEIN-BLOTTED MEMBRANE

Research Project

Project/Area Number 08670267
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Experimental pathology
Research InstitutionNATIONAL CANCER CENTER RESEARCH INSTITUTE

Principal Investigator

TERASAKI Takeo  NATIONAL CANCER CENTER RESEARCH INSTITUTE,PATHOLOGY DIVISION,CHIEF RESEARCHER, 研究所・病理部, 主任研究官 (80142652)

Project Period (FY) 1996 – 1997
Project Status Completed (Fiscal Year 1997)
Budget Amount *help
¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 1997: ¥900,000 (Direct Cost: ¥900,000)
KeywordsII-D cell blot method / cell bolt / protein analysis / tow-dimensional electrophoresis / small cell lung cancer / differentiation / neuronal outgrowth / セル ブロット / 培養細胞
Research Abstract

1.Establishment of Two-Dimensional (II-D) Cell Blot Method.
Partially digested fibronectin with trypsin was two-dimensionally electrophoresed and transferred to a membrane. Protein spots with cell binding domain on the membrane were marked after using specific antibody. Baby hamster kidney (BHK-21) cells were cultured on the membrane over night and membrane sites to where cells attached &ere marked. It was found that sites of protein spots with cell binding domain on the membrane and sites to where BHK-21 cells attached firmly were exactly the same. On the other hand, amino acid sequences of proteins transferred to the membrane can be analysed using amino acid sequencer. It was concluded that analysis of cell binding proteins could be easily done after finding a protein spots on the membrane to where cells attached and analysing amino acid sequences of the protein using amino acid sequenecer after cutting out the spot of the membrane.
2.A new protein that induced differentiation of small cell lung cancer cells to neuronal cells was determined from the conditioned medium of a lung adenocarcinoma cell line using II-D Cell Blot Method and amino acid sequencer.
3.We are planning to analyze proteins concerning cell attachment, cell differenciation or cell death using II-D cell blot method and amino acid sequencer.

Report

(3 results)
  • 1997 Annual Research Report   Final Research Report Summary
  • 1996 Annual Research Report
  • Research Products

    (7 results)

All Other

All Publications (7 results)

  • [Publications] Kazuhiko Tanaka: "Development and Elongation of Neurite-like Outgrowth on Small Cell Lung Cancer Cell Lines" Japanese Journal of Cancer Research. 88・2. 176-183 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Takeo Terasaki: "Two-Dimensional Cell Blot Method" Cell Structure and Function. 23・Sup. 139-139 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Kazuhiko Tanaka: "Development and Elongation of Neurite-like Outgrowth on Small Cell Lung Cancer Cell Lines" Japanese Journal of Cancer Research. 88-2. 176-183 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Takeo Terasaki: "Two-Dimensional Cell Blot Method" Cell Structure and Function. 23-Suppl.139 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Kazuhiko Tanaka: "Development and Elongation of Neurite-like Outgrowth on Small Cell Lung Cancer Cell Lines" Japanese Journal of Cancer Research. 88・2. 176-183 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] 寺崎武夫: "肺腺癌細胞培養上清中に存在する肺小細胞癌培養細胞分化因子の精製" 日本癌学会総会記事. 498-498 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] Kazuhiko Tanaka: "Development and Elongation of Neurite-like Outgrowth on Small Cell Lung Cancer Cell Lines" Japanese Journal of Cancer Research. 88・2. 176-183 (1997)

    • Related Report
      1996 Annual Research Report

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Published: 1997-04-01   Modified: 2016-04-21  

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