Project/Area Number |
05044192
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Research Category |
Grant-in-Aid for international Scientific Research
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Allocation Type | Single-year Grants |
Section | Joint Research |
Research Institution | Nagoya University |
Principal Investigator |
NARUSE Satoru Nagoya University School of Medicine, Lecturer, 医学部, 講師 (50180550)
|
Co-Investigator(Kenkyū-buntansha) |
HERBST F. Biotek Institut, Head, 所長
FORSSMANN W.g. Niedersachsisches Institut fur Peptid-Forschung, Professor, 所長教授
WARY Victor Gesellschaft fur Biotechnologische Forschung, Head, 室長
NOKIHARA Kiyoshi Shimazu Corp.Biotechnology Instr.Dept., Head, バイオ機器部, 研究開発専門部長 (60137073)
OZAKI Tsuyoshi National Institute for physiological Sciences, Associate Professor, 生理学研究所, 助教授 (20045694)
FURUYA Sonoko National Institute for physiological Sciences, Instructor, 生理学研究所, 助手 (20096952)
FORSSMANN W. ニーダーザクセン州立ペプチド研究所, 所長 教授
VICTOR Wray 国立バイオテクノロジー研究所, 主任 研究員
|
Project Period (FY) |
1993 – 1994
|
Project Status |
Completed (Fiscal Year 1994)
|
Budget Amount *help |
¥4,000,000 (Direct Cost: ¥4,000,000)
Fiscal Year 1994: ¥2,000,000 (Direct Cost: ¥2,000,000)
Fiscal Year 1993: ¥2,000,000 (Direct Cost: ¥2,000,000)
|
Keywords | PACAP / PRP / endothelin / secretin / receptor / NMR spectroscopy / radioimmunoassay / 受容体 / セクレチン / NMRスペクトル / 構造活性相関 |
Research Abstract |
The structure of pituitary adenylate activating polypeptide (PACAP) and (PACAP) related peptide (PRP) were investigated by CD and NMR spectroscopy, distance geometry, molecular dynamics and energy minimization calculations. PACAP38 and 27 had an initial disordered N-terminal structure, followed by a helical structures. PRP had a helical structure from 3-20th. Based on these results, several PACAP related peptides were synthesized by a solid phase peptide synthesizer. PACAP was a potent vosodilator. Vascular effects of PACAP was independent of the endothelium and was not blocked by NO synthase inhibitors. PACAP37,36,35,34, and 33 had similar peak vascular effects to PACAP38 but the duration of action was dependent on the length of the peptide. PACAP had an opposite effect to VIP on the guinea pig gallbladder. The C-terminus of PACAP and VIP,where two peptides show the largest difference in sequence, was not important for the recognition of them but the N-terminal flexible portion was responsible for their opposite actions on the gallbladder. Tissue distribution of PACAP38, PACAP27, and PRP in guinea pigs was investigated by radioimmunoassay. Significant amounts of PACAP/PRP were present not only in the central nervous system but also in the gastrointestinal tract, where they were present in the enteric neurons. Several fragments of endothelin and secretin receptors were chemically synthesized and their specific antibodies were raised. On immunoblotts of pancreatic membranes subjected to SDS-polyacrylamide gel electrophoresis, antisera against secretin receptor fragments showed positive bands around 50kDa. Rat pancreatic ducts were strongly stained and acini with less degree by these antisera.
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