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Colorimetric Gene assay Using DNA-Modified Nanoparticles

Research Project

Project/Area Number 13555233
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section展開研究
Research Field 工業分析化学
Research InstitutionKumamoto University

Principal Investigator

YAMABE Kazunori (2002)  Kumamoto Univesity, Faculty of Engineering, Research Associate, 工学部, 助手 (90274696)

井原 敏博 (2001)  熊本大学, 工学部, 講師 (40253489)

Co-Investigator(Kenkyū-buntansha) JYO Akinori  Kumamoto Univesity, Faculty of Engineering, Professor, 工学部, 教授 (40038047)
山部 和則  熊本大学, 工学部, 助手 (90274696)
Project Period (FY) 2001 – 2002
Project Status Completed (Fiscal Year 2002)
Budget Amount *help
¥5,500,000 (Direct Cost: ¥5,500,000)
Fiscal Year 2002: ¥2,500,000 (Direct Cost: ¥2,500,000)
Fiscal Year 2001: ¥3,000,000 (Direct Cost: ¥3,000,000)
KeywordsDNA-modified nanoparticles / colorimetric assay / FRET / SNP analysis / nanotechnology / post-genome / sequence specific aggregation / fluorescence microscopy / 多色アッセイ法 / 一塩基多型解析 / 光の三原色 / ポストゲノム / 超微粒子 / ナノストラクチャー / 凝集体 / 遺伝子診断 / ハイブリダイゼーション / DNA
Research Abstract

1. Preparation of the ODN (oligonudeotide) -modified nanoparticles and preliminary study of their aggregation
Ammo-terminated ODNs were modified onto carboxylates-modified nanoparticles using water soluble carbodiimide (EDAC). Complementary ODN made the particle aggregate under appropriate conditions. The dimension of the aggregates reached tens ofμm and we could easily observe them using ordinary fluorescence microscopy with corresponding optical filters.
2. Aggregates in binary system (red-green)
Two 45 mer ODNs, one of which is a part of wild type p53 gene and the other is the mutant containing one base substitution, were used as model gene samples. Two 25 mer ODNs, each of which contains the 15 nudeotide sequence complementary to each of the terminus of fhe wild type 45 mer, were immobilized onto red and green nanoparticles, respectively. The wild type gathered the both spheres to produce aggregate that emits yellow light (yellow=red+green) under the appropriate conditions. On the other hand, the mutant scarcely affects the distribution of the both spheres. Interestingly the aggregates with the wild type also showed characteristic emission based on the FRET (fluorescence resonance energy transfer) from green particles to closely contacted red particles (from green to red).
3. Aggregates in ternary system (red-green-blue)
Aggregation experiments in binary system mentioned above were extended to the ternary system, in which mixed solution of differently colored (R/G/B) three kinds of tbe ODN-modified nanoparticles were adopted. The wild type and the mutant 45 mers gave the aggregates with yellow (Y=R+G) and magenta (M=R+B) on the whole, respectively.
Improvement of the method for ODN modification onto the particles should help to obtain more distinct results. Colorimetric SNP analysis proposed in this study would be an alternative for high-throughput gene diagnosis and analysis.

Report

(3 results)
  • 2002 Annual Research Report   Final Research Report Summary
  • 2001 Annual Research Report
  • Research Products

    (11 results)

All Other

All Publications (11 results)

  • [Publications] Yasushi Chikaura: "Sequence Specific Aggregation of the Oligonucleotide-Modified Nanoparticles and Its Application to the Colonimetric Gene Detection"Analytical Sciences. 17. 1663-1665 (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Toshihiro Ihara: "DNA Separation Using Zr(IV)-Loaded Resin through Ligand Exchange"Analytical Sciences. 17. 1229-1231 (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Toshihiro Ihara: "Colorimetric SNP analysis using oligonucleotide-modified nanoparticles"Chemical Communications. 2152-2153 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] 井原敏博: "DNA修飾ナノ微粒子を利用したSNPs解析"Bioindustry. 19. 27-35 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Y. Chikaura, S. Tanaka, T. Ihara, A. Jyo: "Sequence Specific Aggregation of the Oligonucleotide-Modified Nanopatticles and Its Application to the Colorimetric Gene Detection"Analytical Sciences. 17. 1163-1165 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] T. Ihara, T. Mitsuru, Y. Kitamura, Y. Chikaura, A. Jyo: "DNA Separation Using Zn(IV)-Loaded Resin through Ligand Exchange"Analytical Sciences. 17. 1163-1165 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] T. Ihara, Y. Chikaura, S. Tanaka, A. Jyo: "Colorimetric SNP Analysis Using Oligonucleotide-Modified Nanoparticles"Chemical Communications. 2152-2153 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] T. Ihara: "SNRs Analysis Using DNA-Modified Nanoparticles"Bioindustiy. 19. 27-35 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Toshihiro Ihara: "Colorimetric SNP analysis using oligonucleotide-modified nanoparticles"Chemical Communications. 2152-2153 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] 井原敏博: "DNA修飾ナノ微粒子を利用したSNPs解析"Bioindustry. 19. 27-35 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] Yasushi Chikaura: "Sequence specific aggregation of the oligonucleotide-modified nanoparticles and its application to the colorimetric gene detection"Analytical Sciences. (in press). (2002)

    • Related Report
      2001 Annual Research Report

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Published: 2001-04-01   Modified: 2016-04-21  

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