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1995 Fiscal Year Final Research Report Summary

Synthetic Study on Neurotrophins and Its Application for Development of Diagnostic Immunoassay Method for Senile Dementia

Research Project

Project/Area Number 05558081
Research Category

Grant-in-Aid for Developmental Scientific Research (B)

Allocation TypeSingle-year Grants
Research Field Bioorganic chemistry
Research InstitutionKYOTO UNIVERSITY

Principal Investigator

FUJII Nobutaka  Kyoto Univ., Fac.of Pharm.Sci., Prof., 薬学部, 教授 (60109014)

Co-Investigator(Kenkyū-buntansha) FUJIMOTO Masafumi  Shionogi Pharm.Co.Research Head, 研究所, 主任研究員
HAYASHI Kyozo  Gifu Pharm.Univ.Emeritus Prof., 名誉教授 (00029935)
IIDA Akira  Kyoto Univ., Fac.of Pharm.Sci.Ass.Prof., 薬学部, 助手 (40202816)
TAMAMURA Hirokazu  Kyoto Univ., Fac.of Pharm.Sci., Ass.Prof., 薬学部, 助手 (80217182)
Project Period (FY) 1993 – 1995
KeywordsSenile Dementia / Alzheimer Disase / Neurotrophin / Chemoselective Purification / Disulfide-bond Formation / Trk-receptor / Tau-protein / Nonhydrolyzable Phosophopeptide
Research Abstract

The following investigations were caried out for development of diagnostic immunoassay method for senile dementia. The report which deny the significant correlation between the plasma levels of neurotrophins and Alzheimer's disease forced us to change the initial plan, however, basic study conducted here should contribute to the future research on daignostic and/or therapeutic use of neurotrophins for senile dementia.
1. A new chemoselective purication method of synthetic peptides based on the bifunctional SH-introducing reagent was developed. In addition, specific affinity purification method using a reversible biotinylating reagent was developed for the final purification of synthetic peptides by solid phase technique.
2. Synthetic study on neuroprophins was carried out in combination with newly-developed chemoseletcive purification method of synthetic peptides and fragment condensation method on solid support. However, low purification yields of Cys-containing peptide fragments and lo … More wering yields in solid phase fragment condensations along with chain elongation compelled us to abandon the total synthesis of neurotrophins.
3. In order to facilitate the final disulfide bond formation of neurotrophins containing three disulfide bonds, new sulfoxide-mediated disulfide bond- forming reactions were developed and successfully applied for unambiguous regioselectie sidulfide-bond formation of several biologically active peptides including anti-HIV peptides and memory enhancing peptides which stimulate NGF synthesis.
4. In order to investigate the intracellular signal transductin pathway of neurotrophin Trk-receptors and the abnormal phosphorylations of Tau-protein associated with Alzheimer's Disease, an efficient synthetic method of phosphopeptides by solid phase technique was developed. Furthermore, stereoselective synthetic methods of phosphatase-resisted phosphoaminoacids mimetics and (E) -alkene-dipeptide isoseres as nonhydrolyzable dipeptide mimetics were investigated. These nonhydrolyzable phosphopeptide mimetics will serve as useful tools for biochemical study on protein phosphorylation associated with Alzheimer's disease. Less

  • Research Products

    (13 results)

All Other

All Publications (13 results)

  • [Publications] S. Funakoshi, et al.: "Affinity Purification Method Using a Reversible Biotinylating Reagent for Peptides Synthesized by the Solid-Phase Technique." J. Choromatogr.638. 21-27 (1993)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] T. Koide, et al.: "Investiation of the Dimethylsulfoxide-Trifluoroacetic Acid Oxidation System for the Synthesis of Cystine-Containing Peptides." Chem. Pharm. Bull.,. 41. 1030-1034 (1993)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] A. Otaka, et al.: "Synthesis and Application of N-Boc-L-2-Amino-4-(Diethylphosphono)-4,4-Difluorobutanoic Acid for Solid Phase Synthesis of Nonhydrolyzable Phosphoserine Peptide Analogs." Tetrahedron Lett.,. 36. 927-930 (1995)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] H. Tamamura, et al.: "Disulfide Bond-Forming Reaction using a Dimethylsulfoxide/aqueous HCl System and Its Application to Regioselective Two Disulfide Bond Formation." Int. J. Peptide Protein Res.,. 45. 312-319 (1995)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] N. Fujii, et al.: "SN2'Ring Opening Reaction of Azridines bearing an α,β-Unsaturated Ester Group with Organocopper Reagents. A New Stereoselective Synthetic Route to(E)-Alkene Dipeptide Isosteres." J. Chem. Soc., Perkin I. 1995. 1359-1371 (1995)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] A. Otaka, et al.: "Development of Efficient Two-Step Deprotection Methodology for Dimethyl-Protected Phosphoamino Acids-containing Peptide Resins and Its Application to the Practical Synthesis of Phosphopeptides." J. Org. Chem.,. 60. 3967-3974 (1995)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] H. Tamamura, et al.: "Synthesis of Protegrin-Related Peptides and Their Antibacterial and Anti-Human Immunodeficiency Virus Activity." Chem. Pharm. Bull.43. 853-858 (1995)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] S.Funakoshi, et al.: "Affinity Purification Method Using a Reversible Biotinylating Reagent for Peptides Synthesized by the Solid-Phase Technique." J.Choromatogr. 638. 21-27 (1993)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] T.Koide, et al.: "Investiation of the Dimethylsulfoxide-Trifluoroacetic Acid Oxidation System for the Synthesis of Cystine-Containing Peptides." Chem.Pharm.Bull.41. 1030-1034 (1993)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] A.Otaka, et al.: "Synthesis and Application of N-Boc-L-2-Amino-4- (Diethylphosphono) -4,4-Difluorobutanoic Acid for Solid Phase Synthesis of Nonhydrolyzable Phosphoserine Peptide Analogs." Tetrahedron Lett.36. 927-930 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] H.Tamamura, et al.: "Disulfide Bond-Forming Reaction using a Dimethylsulfoxide/aqueous HC1 System and Its Application to Regioselective Two Disulfide Bond Formation." Int.J.Peptide Protein Res.45. 312-319 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] N.Fujii, et al.: "SN2' Ring Opening Reaction of Aziridines bearing an alpha, beta-Unsaturated Ester Group with Organocopper Reagents. A New Stereoselective Synthetic Route to (E) -Alkene Dipeptide Isosteres." J.Chem.Soc., Perkin I. 1995. 1359-1371 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] A.Otaka, et al.: "Development of Efficient Two-Step Deprotection Methodology for Dimethyl-Protected Phosphoamino Acids-containing Peptide Resins and Its Application to the Practical Synthesis of Phosphopeptides." J.Org.Chem.60. 3967-3974 (1995)

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 1997-03-04  

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