Role of chloride ion in the dynamics of microtubule
Project/Area Number |
20790176
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Single-year Grants |
Research Field |
General physiology
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Research Institution | Kyoto Prefectural University of Medicine |
Principal Investigator |
NAKAJIMA Ken-ichi Kyoto Prefectural University of Medicine (40398392)
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Project Period (FY) |
2008 – 2009
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Project Status |
Completed (Fiscal Year 2009)
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Budget Amount *help |
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2009: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2008: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
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Keywords | 細胞骨格 / クロライドイオン / GTPase |
Research Abstract |
Microtubules are fundamental cytoskeletal systems in eukaryotic cells. Microtubule, assembled from heterodimers of α- and β-tubulin, are cylindrical polymers whose in vitro assembly from subunits requires GTP (only GTP-bound form of β-tubulin can assembled into polymer and GTP is hydrolysed to GDP just after assembly). In this study, we investigated the role of various anions, especially chloride ion, in polymerization and GTPase activity of tubulin. 1. The effect of various anions on microtubule polymerization In the presence of Cl^-, F^- and gluconate, effective in vitro microtubule polymerization was observed. In the presence of Br^-, NO_3^-, or I^-, weak polymerizaion was observed. 2. The effect of various anions on tubulin GTPase activiy GTPase activiy of tubulin was measured, and found that high activity was observed in the presence of Br^- or NO_3^-, and weak activiy was observed in the presence of Cl^-, F^- and gluconate. These observations indicated that some anions such as Cl^-, F^- and gluconate promoted polymerization of microtubules, via suppression of GTPase activity of tubulin.
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Report
(3 results)
Research Products
(15 results)
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[Journal Article] Regulation of paracellular Na+ and Cl- conductances by the hydrostatic pressure.2009
Author(s)
Tokuda S, Niisato N, Nagai T, Taruno A, Nakajima K, Miyazaki H, Yamada T, Hosogi S, Ohta M, Nishio K, Iwasaki Y, Marunaka Y.
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Journal Title
Cell Biol. Int. 33
Pages: 949-956
Related Report
Peer Reviewed
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