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完整後設資料紀錄
DC 欄位 | 值 | 語言 |
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dc.contributor.advisor | 郭鐘金(Chung-Chin Kuo) | |
dc.contributor.author | Yu-Chang Chou | en |
dc.contributor.author | 周鈺章 | zh_TW |
dc.date.accessioned | 2021-06-15T06:45:40Z | - |
dc.date.available | 2016-10-05 | |
dc.date.copyright | 2011-10-05 | |
dc.date.issued | 2011 | |
dc.date.submitted | 2011-08-19 | |
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dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/48075 | - |
dc.description.abstract | NMDA受體(N-methyl-D-aspartate receptor, NMDAR)是一種麩胺酸受體(Glutamate Receptor),與其他麩胺酸受體最大的不同處在於其高度的鈣離子通透性、以及鎂離子對其賦予的電壓依賴性。也因此,除了突觸訊息的傳遞外,NMDA受體也參與了突觸可塑性、學習記憶整合等高層級神經生理上的調控。NMDAR由四個次單元所構成,每個次單元皆有四個穿膜區段,其中第二穿膜區段為構成孔洞內壁最主要的部份。過去的研究指出,位於第二穿膜區段的尖端上,NR1的N616或是NR2B的N615、N616這幾個結構上較為相近的胺基酸,若將其突變則會對鈣離子的通透性、以及鎂離子的抑制性造成很大的影響。本實驗藉由patch clamp的技術來記錄表現在非洲爪蟾蛙卵上的重組NR1-NR2B電流,測量外側的鎂離子、鈣離子在不同電壓下通透的情形。發現 NR1與NR2B的N site其功能分別對鎂離子和鈣離子的通透性影響是有差異的。在極負電壓下,鎂離子可以穿過NMDAR,NR1 N616突變後會僅會些微增加極負電壓下鎂離子的通透性,而NR2B N615的突變會明顯改變鎂離子與NMDAR之間的親和力。NR1 N616的突變則也會對鈣離子和鈉離子的通透電流造成影響。此外鎂離子和鈣離子都會對NMDAR的門閥性質有影響,特別是作用在NR1 N616上。綜合以上幾點可以發現,NMDAR次單元具有功能性的不對稱性。NR1與NR2B的N site分別與鈣離子和鎂離子的通道阻斷作用較為有關。 | zh_TW |
dc.description.abstract | N-methyl-D-aspartate receptors(NMDARs) are subtypes of ionotropic glutamate receptors that have distinct characteristics including high permeability to calcium ions and voltage-dependant block by magnesium ion. Thus, NMDARs play an important role in neural transmission, neuronal plasticity and long-term potentiation. NMDAR is composed of four subunits, and each subunits have four transmembrane domains(M1-4). The re-entrant loop (M2) forms part of the channel pore. The amino acid on the tip of M2 loop, like NR1-N616 and NR2B-N615, play an important role in Mg2+ block and divalent cation permeability. In this study, we examined the mechanism of extracellular calcium permeability and Mg2+ block in recombinant NR1-NR2B expressed on Xenopus oocytes. The NMDAR currents were measured with excised outside-out macropatchs. We found that Mg2+ could permeate through NMDAR in extreme low voltage. The mutant NR2B containing N615Q and N615C may increase external Mg2+ permeability and decrease binding affinity ,which indicate that the NR2B N615 may be the energy barrier for Mg2+ permeation in the pore. NR1 N616Q increase the permeability of Mg2+ in extreme low voltage, and also has a strong influence on calcium permeability. We conclude that the subunits of NMDAR do not have a completely symmetric alignment in tense of permeation of divalent ions. | en |
dc.description.provenance | Made available in DSpace on 2021-06-15T06:45:40Z (GMT). No. of bitstreams: 1 ntu-100-R96441010-1.pdf: 6127960 bytes, checksum: e4b258a290301993f459ad85da6f83b4 (MD5) Previous issue date: 2011 | en |
dc.description.tableofcontents | 中文摘要...................................................................................1
英文摘要...................................................................................2 導論.........................................................................................3 材料與方法................................................................................7 結果..........................................................................................9 討論........................................................................................14 圖...........................................................................................18 參考文獻..................................................................................33 | |
dc.language.iso | zh-TW | |
dc.title | NMDA受體的二價陽離子通透性及通道阻斷之分子機制 | zh_TW |
dc.title | The molecular mechanism underlying divalent ions permeation and block of NMDA receptors | en |
dc.type | Thesis | |
dc.date.schoolyear | 99-2 | |
dc.description.degree | 碩士 | |
dc.contributor.oralexamcommittee | 湯志永,黃榮棋 | |
dc.subject.keyword | NMDA受體,鎂離子,鈣離子,通透,阻斷,能量屏障, | zh_TW |
dc.subject.keyword | NMDAR,magnesium,calcium,permeation,block,energy barrier, | en |
dc.relation.page | 38 | |
dc.rights.note | 有償授權 | |
dc.date.accepted | 2011-08-20 | |
dc.contributor.author-college | 醫學院 | zh_TW |
dc.contributor.author-dept | 生理學研究所 | zh_TW |
顯示於系所單位: | 生理學科所 |
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