論文使用權限 Thesis access permission:校內外都一年後公開 withheld
開放時間 Available:
校內 Campus: 已公開 available
校外 Off-campus: 已公開 available
論文名稱 Title |
固態核磁共振中選擇性重聚脈衝期間的異核去偶優化初探 Preliminary Investigation on the Optimization of Heteronuclear Decoupling During Selective Refocusing Pulse in Solid State Nuclear Magnetic Resonance |
||
系所名稱 Department |
|||
畢業學年期 Year, semester |
語文別 Language |
||
學位類別 Degree |
頁數 Number of pages |
65 |
|
研究生 Author |
|||
指導教授 Advisor |
|||
召集委員 Convenor |
|||
口試委員 Advisory Committee |
|||
口試日期 Date of Exam |
2007-06-28 |
繳交日期 Date of Submission |
2007-07-21 |
關鍵字 Keywords |
生物大分子、固態NMR異核去偶評述、選擇性脈衝、固態核磁共振、對稱理論 solid-state NMR, heteronuclear decoupling, symmetry-based theory, selective pulses |
||
統計 Statistics |
本論文已被瀏覽 5690 次,被下載 1114 次 The thesis/dissertation has been browsed 5690 times, has been downloaded 1114 times. |
中文摘要 |
異核去偶是固態NMR取得高解析度至關重要的方法。目前已有許多異核去偶方法被開發出來,諸如TPPM,XiX,SPINAL,以及近年來的對稱型脈衝序列和eDROOPY等。然而,這些序列大多是針對自由演化和長方脈衝期間的體系進行去偶,並不考慮自旋體系的即時狀態。而在形狀化脈衝期間,去偶脈衝對演化及去偶效果的影響和最佳化,據我們所知,還未有人系統性地研究過。 本研究嘗試由形狀化重聚脈衝著手,試圖在脈衝期間,進行形狀化的去偶。我們選擇了r-SNOB和Gaussian等常用的選形重聚脈衝,並在重聚脈衝期間,分別以連續波,長脈衝,TPPM,Gaussian和Sinc等脈衝進行去偶。從我們所獲得的光譜中,發現了一些過去從未在固態NMR中發現的新現象。我們的研究結果顯示,若選形重聚脈衝期間,功率未達閾值,即將所有訊號消除。另外許多選形脈衝具有顯著去相的效果。本研究初步驗證了形狀脈衝期間的去偶的圖像,和自旋回波整體的去偶,在自旋演化上是存在差異的。 |
Abstract |
none |
目次 Table of Contents |
目錄 1. 緒論……………………………………………………………………………………………….1 第一部份:背景與原理 2. 固態NMR異核去偶評述……………………………………………………………….4 2.1 異核偶極偶合……………………………………………………………………………….4 2.2 異核去偶概論……………………………………………………………………………….5 2.3 異核去偶方法……………………………………………………………………………….8 2.4 對稱理論與異核去偶探討…………………………………………………...………...12 2.4.1 座標變換……………………………………………………………………………...12 2.4.2 射頻Euler角.............................................................................................16 2.4.3 對稱類型...................................................................................................17 2.4.4 平均Hamiltonian理論和對稱選擇律.....................................................21 2.4.5 對稱選擇律與異核去偶...........................................................................24 3. 選擇性形狀脈衝概論.........................................................................29 3.1 緒論..................................................................................................................29 3.2 基本原理..........................................................................................................31 第二部分:實驗 4. 實驗.....................................................................................................35 4.1 實驗設計..........................................................................................................35 4.2 儀器簡介......................................................................................................... 35 4.3 脈衝序列及參數..............................................................................................36 4.3.1 CP/MAS 實驗...........................................................................................36 4.3.2 重聚脈衝序列.......................................................................................... 37 5. 結果,討論,結論與展望..................................................................40 5.1 實驗結果..........................................................................................................40 5.2 結果討論..........................................................................................................57 5.3 結論..................................................................................................................58 5.4 展望..................................................................................................................59 |
參考文獻 References |
參考文獻 1. [1] J. Wang, S. Kim, F. Kovacs, T.A. Cross, Structure of the transmembrane region of the M2 protein H+ channel, Protein Sci. 10 (2001), 2241 [2] R. Mani, M. Tang, X. Wu, J.J. Buffy, A.J. Waring, M.A. Sherman, M. Hong, Membrane-bound dimer structure of a α-Hairpin antimicrobial peptide from rotational-echo double-resonance solid-state NMR, Biochemistry 45 (2006) 8341 [3] S.H. Park, A.A. Mrse, A.A. Nevzorov, M.F. Mesleh, M. Oblatt-Montal, S.J. Opella, Three-dimensional structure of the channel-forming transmembrane domain of virus protein “u” (Vpu) from HIV-1, J. Mol. Biol. 333 (2003) 409 [4] Y.H. Tseng, C.Y. Mou, J.C.C. Chan, Solid-State NMR study of the transformation of octacalcium phosphate to hydroxyapatite: a mechanistic model for central darkline formation, J. Am. Chem. Soc. 128 (2006) 6909 [5] T. Asakura, M. Okonogi, Y. Nakazawa, K. Yamauchi, Structural analysis of alanine tripeptide with antiparallel and parallel β-Sheet structures in relation to the analysis of mixed β-Sheet structures in Samia cynthia ricini silk protein fiber using solid-state NMR spectroscopy, J. Am. Chem. Soc. 128 (2006) 6231 [6] A.T. Petkova, R.D. Leapman, Z. Guo, W.M. Yau, M.P. Mattson, and R. Tycko, Self-propagating, molecular-level polymorphism in Alzheimer’s β-amyloid fibrils, Science 307 (2005) 262 [7] A.E. Bennett, C.M. Rienstra, M. Auger, K.V. Lakshmi, R.G. Griffin, Heteronuclear decoupling in rotating solids, J. Chem. Phys. 103 (1995) 6951 [8] Z.H. Gan, R.R. Ernst, Frequency- and phase-modulated heteronuclear decoupling in rotating solids, Solid State NMR 8 (1997) 153 [9] R.S. Thakur, N.D. Kurur, P.K. Madhu, Swept-frequency two-pulse phase modulation for heteronuclear dipolar decoupling in solid-state NMR, Chem. Phys. Lett. 426 (2006) 459 [10] B.M. Fung, A.K. Khitrin, K. Ermolaev, An improved broadband decoupling sequence for liquid crystals and solids, J. Magn. Reson. 142 (2000) 97 [11] M. Ed |
電子全文 Fulltext |
本電子全文僅授權使用者為學術研究之目的,進行個人非營利性質之檢索、閱讀、列印。請遵守中華民國著作權法之相關規定,切勿任意重製、散佈、改作、轉貼、播送,以免觸法。 論文使用權限 Thesis access permission:校內外都一年後公開 withheld 開放時間 Available: 校內 Campus: 已公開 available 校外 Off-campus: 已公開 available |
紙本論文 Printed copies |
紙本論文的公開資訊在102學年度以後相對較為完整。如果需要查詢101學年度以前的紙本論文公開資訊,請聯繫圖資處紙本論文服務櫃台。如有不便之處敬請見諒。 開放時間 available 已公開 available |
QR Code |