Mechanism of large protein secretion coordinated by the small GTPase and the ER-resident proteins
Project/Area Number |
22770120
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Single-year Grants |
Research Field |
Functional biochemistry
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Research Institution | The University of Tokyo |
Principal Investigator |
SAITO Kota 東京大学, 大学院・薬学系研究科, 助教 (60549632)
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Project Period (FY) |
2010 – 2011
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Project Status |
Completed (Fiscal Year 2011)
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Budget Amount *help |
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2011: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2010: ¥2,730,000 (Direct Cost: ¥2,100,000、Indirect Cost: ¥630,000)
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Keywords | 分泌 / コラーゲン / 小胞体 / COPII / 癌 |
Research Abstract |
Collagen synthesized in the ER is too big to fit into conventional transport carriers and the mechanism how collagens export from the ER is still largely unclear. Here we show that cTAGE5 localizes to the ER exit sites and forms a complex with TANGO1, a previously characterized cargo receptor for collagen VII. cTAGE5 as well as TANGO1 is required for collagen VII secretion. We propose that cTAGE5 acts as a co-receptor of TANGO1 for collagen VII export from the ER.
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Report
(3 results)
Research Products
(14 results)
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[Journal Article] cTAGE5 mediates collagen secretion through interaction with TANGO1 at endoplasmic reticulum exit sites2011
Author(s)
Saito, K., Yamashiro, K., Ichikawa, Y., Erlmann, P., Kontani, K., Malhotra, V., and Katada, T.
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Journal Title
Mol Biol Cell
Volume: 22
Issue: 13
Pages: 2301-2308
DOI
Related Report
Peer Reviewed
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