| Project/Area Number |
04044112
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| Research Category |
Grant-in-Aid for international Scientific Research
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| Allocation Type | Single-year Grants |
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| Section | Joint Research |
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| Research Institution | THE UNIVERSITY OF TOKYO |
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Principal Investigator |
MIKOSHIBA Katsuhiko THE INSTITUTE OF MEDICAL SICIENCE THE UNIVERSITY OF TOKYO : PROFESSOR, 医科学研究所, 教授 (30051840)
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| Co-Investigator(Kenkyū-buntansha) |
SOLOMON Snyd ジョンズホプキンス大学, 医学部神経科学教室, 主任教授
SNYDER Solomon JOHNS HOPKINS UNIVERSITY SCHOOL MEDICINE : PROFESSOR
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| Project Period (FY) |
1992 – 1993
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| Project Status |
Completed (Fiscal Year 1993)
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| Budget Amount *help |
¥5,300,000 (Direct Cost: ¥5,300,000)
Fiscal Year 1993: ¥2,300,000 (Direct Cost: ¥2,300,000)
Fiscal Year 1992: ¥3,000,000 (Direct Cost: ¥3,000,000)
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| Keywords | IP3RECEPTOR / CALCIUM / ENDOPLASMIC RETICULUM / IP3 / CALCIUM RELEASE / Ca^<2+>波 / 受精 / イノシトール3リン酸(IP_3) / Ca^<2+>放出能 / Ca^<2+>チャネル |
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| Research Abstract |
With exchanging ideas of localization of IP3 receptor (IP3R) on the plasma membrane, we both detected the reaction on the plasma membrane on caveola structure(by our group) of smooth muscle cells and others and T cell(by Snyder's group).
We established a novel method to isolate a single type of inositol 1, 4, 5-trisphosphate receptor(IP3R) among the heterogenous population of receptors, to study the regulatory mechanism of Ca2+ release.
Both the rate and extent of 45Ca2+ influx into proteoliposomes were increased 20% after incubation with the catalytic subunit of cyclic AMP-dependent protein kinase(PKA) contrary to Snyder's data It was accompanied by stoichiometric phosphorylation of IP3 receptor protein.
Transmembrance topology of IP3R was analyzed by two approaches using immunocytochemical and molecular biological techniques. The immunocytochemical study using the site-specific antibody showed that the residues 2504-2523 are located in the luminal side of the ER. Among the 20 putative glycosylation site only two were the candidates of N-glycosylation. By ConA column chromatography of the site-directed mutant receptors, both Asn-2475 and Asn-2503 were glycosylated, indication the these two Asn residues are located in the ER luminal side. These results suggested that IP3R traverses the membrance six times.
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