Skip navigation

DSpace

機構典藏 DSpace 系統致力於保存各式數位資料(如:文字、圖片、PDF)並使其易於取用。

點此認識 DSpace
DSpace logo
English
中文
  • 瀏覽論文
    • 校院系所
    • 出版年
    • 作者
    • 標題
    • 關鍵字
    • 指導教授
  • 搜尋 TDR
  • 授權 Q&A
    • 我的頁面
    • 接受 E-mail 通知
    • 編輯個人資料
  1. NTU Theses and Dissertations Repository
  2. 理學院
  3. 化學系
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/28966
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor陳昭岑(Chao-Tsen Chen)
dc.contributor.authorYu-Fen Chenen
dc.contributor.author陳玉芬zh_TW
dc.date.accessioned2021-06-13T00:32:15Z-
dc.date.available2010-07-30
dc.date.copyright2007-07-30
dc.date.issued2007
dc.date.submitted2007-07-26
dc.identifier.citation1. (a) Lopez-Otin, C.; Overall, C. M. Nature Rev. Mol. Cell Biol. 2002, 3, 509. (b) Elaine, W. S.; Chattopadhaya, S.; Panicker, R. C.; Huang, X.; Yao, S. Q. J. Am. Chem. Soc. 2004, 126, 14435. (c) Belshaw, P. J.; Levitsky, K.; Ciolli, C. J. Org. Lett. 2003, 5, 693. (d) Belshaw, P. J.; Schoepfer, J. G.; Liu, K. Q.; Morrison, K. L.; Schreiber, S. L. Angew. Chem., Int. Ed. Engl. 1995, 34, 2129.
2. (a) Humphery, S. I.; Hochstrasser, D. F.; Williams, K. L. Biotech. Gen. Eng. Rev. 1995, 13, 19. (b) Venter, J. C.; Adams, M. D.; Myers, E. W.; Li, P. W. Science 2001, 291, 1304.
3. 王惠鈞,吳啟裕(2005),第二章 蛋白質體學之新進展,http://bbsc.imb.sinica.edu.tw/biotech/02_03.pdf
4. (a) Lai, R. Cancer 2002, 85, 1071. (b) Ritchie, R. F.; Palomaki, G. E.; Neveux, L. M.; Navolotskaia, O. J. Clin. Lab. Anal. 1999, 13, 280.
5. Patterson, S. D.; Aebersold, R. H. Nature Genetics 2003, 33, 311.
6. Gygi, S. P.; Rist, B.; Turecek, F.; Gelb, M. H.; Aebersold, R. Nat. Biotechnol 1999, 17, 994.
7. (a) Liu, Y.; Patricelli, M. P.; Cravatt, B. F. Proc. Natl. Acad. Sci. USA 1999, 96, 14694. (b) Uetz, P. Curr. Opin. Chem. Biol. 2002, 6, 57.
8. (a) Zhu, H.; Bilgin, M.; Bangham, R. Science 2001, 293, 2101. (b) Macbeath, G.; Schreiber, S. Science 2000, 289, 1760.
9. (a) Adam, G. C.; Cravatt, B. F.; Sorensen, E. J. Chem. Biol. 2001, 8, 81. (b) Adam, G. C.; Sorensen, E. J.; Cravatt, B. F. Nat. Biotechnol. 2002, 20, 805. (c) Adam, G. C.; Sorensen, E. J.; Cravatt, B. F. Mol. Cell. Proteomics 2002, 1, 828. (d) Jessani, N.; Cravatt, B. F. Curr. Opin. Chem. Biol. 2004, 8, 54. (e) Adam, G. C.; Cravatt, B. F. J. Am. Chem. Soc. 2004, 126, 1363.
10. Bruno, D.; Samuel, B. J. Proteome. Res. 2004, 3, 4.
11. Henzel, W. J.; Billeci, T. M.; Stults, J. T.; Wong, S. C.; Grimley, C. Proc. Natl. Acad. Sci. USA 1993, 90, 5011.
12. Yarmush, M. L.; Jayaraman, A. Annu. Rev. Biomed. Eng. 2002, 4, 349.
13. Gygi, S. P.; Corthals, G. L.; Zhang, Y.; Rochon, Y.; Aebersold, R. Proc. Natl. Acad. Sci. USA 2000, 97, 9390.
14. Gygi, S. P.; Rist, B.; Aebersold, R. Curr. Opin. Biotechnol. 2000, 11, 396.
15. Evans, M. J.; Cravatt, B. F. Chem. Rev. 2006, 106, 3279.
16. (a) Ichikawa, M.; Ichikawa, Y. Bioorg. Med. Chem. Lett. 2001, 11, 1769. (b) Tsai, C. S.; Li, Y. K.; Lo, L. C. Org. Lett. 2002, 4, 3607. (c) Vocadlo, D.; Bertozzi, C. R. Angew. Chem. Int. Ed. 2004, 43, 5338. (d) Williams, S. J.; Hekmat, O.; Withers, S. G. ChemBioChem 2006, 7, 116.
17. (a) Liu, Y.; Patricelli, M. P.; Cravatt, B. F. Proc. Natl. Acad. Sci. USA 1999, 96, 14694. (b) Kidd, D.; Liu, Y.; Cravatt, B. F. Biochemistry 2001, 40, 4005.
18. (a) Faleiro, L.; Kobayashi, R.; Fearnhead, H.; Lazebnik, Y. A. EMBO J. 1997, 16, 2271. (b) Greenbaum, D.; Medzihradszky, K. F.; Burlingame, A.; Bogyo, M. Chem. Biol. 2000, 7, 569.
19. Cohen, M. S.; Zhang, C.; Shokat, K. M.; Taunton, J. Science, 2005, 308, 1318.
20. (a) Lo, L. C.; Pang, T. L.; Kuo, C. H.; Chiang, Y. L.; Wang, H. Y.; Lin, J. J. J. Proteome Res. 2002, 1, 35. (b) Kumar, S.; Zhou, B.; Liang, F.; Wang, W. Q.; Huang, Z.; Zhang, Z. Y. Proc. Natl. Acad. Sci. USA 2004, 101, 7943.
21. (a) Liu, Y.; Patricelli, M. P.; Cravatt, B. F. Proc. Natl. Acad. Sci. USA 1999, 96, 14694. (b) Kidd, D.; Liu, Y.; Cravatt, B. F. Biochemistry 2001, 40, 4005. (c) Patricelli, M. P.; Giang, D. K.; Stamp, L. M.; Burbaum, J. J. Proteomics 2001, 1, 1067.
22. (a) Shaw, E. Methods Enzymol. 1994, 244, 649. (b) Shaw, E.; Angliker, H.; Rauber, P.; Walker, B.; Wikstrom, P. Biomed. Biochim. Acta 1986, 45, 1397.
23. Palmer, J. T.; Rasnick, D.; Klaus, J. L.; Bromme, D. J. Med. Chem. 1995, 38, 3193.
24. (a) Bromme, D.; Schierhorn, A.; Kirschke, H.; Wiederanders, B.; Barth, A.; Fittkau, S.; Demuth, H. U. Biochem. J. 1989, 263, 861. (b) Brady, K. D.; Giegel, D. A.; Grinnell, C.; Lunney, E.; Talanian, R. V.; Wong, W.; Walker, N. Bioorg. Med. Chem. 1999, 7, 621. (c) Pliura, D. H.; Bonaventura, B. J.; Smith, R. A.; Coles, P. J.; Krantz, A. Biochem. J. 1992, 288, 759.
25. Drahl, C.; Cravatt, B. F.; Sorensen, E. J. Angew. Chem., Int. Ed. 2005, 44, 5788.
26. Barrett, A. J.; Kembhavi, A. A.; Brown, M. A.; Kirschke, H.; Knight, C. G.; Tamai, M.; Hanada, K. Biochem. J. 1982, 201, 189.
27. Barrett, A. J. Protease Inhibitors; Elsevier: Amsterdam, 1980.
28. (a) Bogyo, M.; Verhelst, S.; Bellingard-Dubouchaud, V.; Toba, S.;Greenbaum, D. Chem. Biol. 2000, 7, 27. (b) Greenbaum, D.; Medzihradszky, K. F.; Burlingame, A.; Bogyo, M. Chem. Biol. 2000, 7, 569. (c) Greenbaum, D. C.; Arnold, W. D.; Lu, F.; Hayrapetian, L.; Baruch, A.; Krumrine, J.; Toba, S.; Chehade, K.; Bromme, D.; Kuntz, I. D.; Bogyo, M. Chem. Biol. 2002, 9, 1085.
29. (a) Kim, D. H.; Mobashery, S. Curr. Med. Chem. 2001, 8, 959. (b) Schultz, G. S.; Strelow, S.; Stern, G. A.; Chegini, N.; Grant, M. B.; Galardy, R. E.; Grobelny, D.; Rowsey, J. J.; Stonecipher, K.; Parmley, V.; et al. Invest. Ophthalmol. Visual Sci. 1992, 33, 3325. (c) Ramnath, N.; Creaven, P. J. Curr. Oncol. Rep. 2004, 6, 96.
30. Chang, C.; Werb, Z. Trends Cell Biol. 2001, 11, S37.
31. Whittaker, M.; Floyd, C. D.; Brown, P.; Gearing, A. J. Chem. Rev. 1999, 99, 2735.
32. Chowdry, V.; Westheimer, F. H. Annu. Rev. Biochem. 1979, 48, 293.
33. (a) Adam, G. C.; Cravatt, B. F.; Sorensen, E. J. Chem. Biol. 2001, 8, 81. (b) Adam, G. C.; Sorensen, E. J.; Cravatt, B. F. Nat. Biotechnol. 2002, 20, 805. (c) Adam, G. C.; Burbaum, J.; Kozarich, J. W.; Patricelli, M. P.; Cravatt, B. F. J. Am. Chem. Soc. 2004, 126, 1363.
34. Barglow, K. T.; Cravatt, B. F. Chem. Biol. 2004, 11, 1523.
35. Dwek, R. A.; Lellouch A. C.; Wormald M. R. J. Anatomy 1995, 187, 279.
36. Fischer, E. Ber. Dtsch. Chem. Ges. 1890, 23, 2114.
37. (a) Avery, O. T.; Heidelberger, M. J. Exp. Med. 1923, 38, 73. (b) Dubos, R.; Avery, O. T. J. Exp. Med. 1931, 54, 51.
38. (a) Jentoft, N. Trends Biochem. Sci. 1990, 15, 291. (b) Berg, E. I.; Robinson, M. K.; Warnock, R. A.; Butcher, E. C. J. Cell Biol. 1991, 114, 343. (c) Lasky, L. A. Science 1992, 258, 964. (d) Malhotra, R.; Taylor, N. R.; Bird, M. I. Biochem. J. 1996, 314, 297. (e) Somers, W. S.; Tang, J.; Shaw, G. D.; Camphausen, R. T. Cell 2002, 103, 467. (f) Brandley, B. K.; Kiso, M.; Abbas, S.; Nikrad, P.; Srivasatava, O.; Foxall, C.; Oda, Y.; Hasegawa, A. Glycobiology 1993, 3, 633. (g) Ramphal, J. Y.; Zheng, Z.-L.; Perez, C.; Walker, L. E.; DeFrees, S. A.; Gaeta, F. C. A. J. Med. Chem. 1994, 37, 3459. (h) Wu, S. H.; Shimazaki, M.; Lin, C. C.; Qiao, L.; Moree, W. J.; Weitz-Schmidt, G.; Wong, C. H. Angew. Chem. Inl. Ed Engl. 1996, 35, 88. (i) Osbon, L. Cell 1990, 62, 3. (j) Wong, C. H. Riken Review 1995, 8, 3. (k) Frenette, P. S.; Wagner, D. D. Molecular Medicine 1996, 335, 43. (l) Mileski, W. J.; Winn, R. K.; Vedder, N. B.; Pohlman, T. H.; Harlan, J. M.; Rice, C. L. Surgery 1990, 108, 206. (m) Aruffo, A.; Kolanus, W.; Walz, G.; Fredman, P.; Seed, B. Cell 1991, 67, 35. (n) 劉秉彥;陳志鴻 科學發展 2004, 352, 48. (o) Israelian-Konaraki, Z.; Reaven, P. D. Cardiology 2005, 103, 1. (p) Ochi, T.; Hakomori, S. I.; Fujimoto, M.; Okamura, M.; Owaki, H.; Wakitani, S.; Shimaoka, Y.; Hayashida, K.; Tomita, T.; Kawamura, S.; Ono, R. J. Rheumatol. 1993, 20, 2038. (q) Hayashi, M.; Tanaka, M.; Itoh, M.; Miyauchi, H. J. Org. Chem. 1996, 61, 2938. (r) Thoma, G.; Schwarzenbach, F.; Duthale, R. O. J. Org. Chem. 1996, 61, 514. (s) Wong, C. H.; Moris-Varas, F.; Hung, S. C.; Marron, T. G.; Lin, C. C.; Gong, K. W.; Weitz-Schmidt, G. J. Am. Chem. Soc. 1997, 119, 8125. (t) Berg, E. I.; Robinson, M. K.; Warnock, R. A.; Butcher, E. C. J.Cell Biol. 1991, 114, 343.
39. Sears, P.; Wong, C. H. Cell. Mol. Life Sci. 1998, 54, 223.
40. Geijtenbeck, Y.; Torensama, R.; van Vliet, S.; van Duijnhoven, G.; Adema, G.; van Kooyk, Y.; Figdor, C. Cell 2000, 100, 575.
41. (a) Sacchettini, J. C.; Baum, L. G.; Brewer, C. F. Biochemistry 2001, 40, 3009. (b) Ratner, D. M.; Adams, E. W.; Disney, M. D. Seeberger, P. H. ChemBioChem 2004, 5, 1375.
42. Kansas, G. Blood 1996, 88, 3259.
43. (a) Feizi, T. Carbohydr. Chem. Biol. 2000, 4, 851. (b) Gestwicki, J. E.; Kiessling, L. L. Nature, 2002, 415, 81.
44. Scigelova, M.; Singh, S.; Crout, D. H. G. J. Mol. Catal. B: Enzym. 1999, 6, 483.
45. Hers, H. G. Gastroenterology 1965, 48, 625.
46. Barton, N. W.; Furbish, F. S.; Murray, G. J.; Garfield, M.; Brady, R. O. Proc. Natl. Acad. Sci. USA 1990, 87, 1913.
47. (a) Winchester, B.; Fleet, G. W. J. J. Carbohydr. Chem. 2000, 19, 471. (b) Clissold, S. P.; Edwards, C. Drugs 1988, 35, 214.
48. (a) Humphries, M. J. Cancer Res. 1986, 46, 5212. (b) Nishimura, Y.; Satoh, T.; Adachi, H.; Kondo, S.; Takeuchi, T.; Azetaka, M.; Fukuyasu, H.; Iizuka, Y. J. Med. Chem. 1997, 40, 2626.
49. (a) Karpas, A.; Fleet, G. W. J.; Dwek, R. A.; Petursson, S.; Namgoong, S. K.; Ramsden, N. G.; Jacob, G. S.; Rademacher, T. W. Proc. Natl. Acad. Sci. USA 1988, 85, 9229. (b) Karlsson, G. B.; Buttlers, T. D.; Dwek, R. A.; Platt, F. M. J. Biol. Chem. 1993, 268, 570.
50. Coughlan, M. P.; Hazlewood, G. Biotechnol Appl Biochem 1993, 17, 259.
51. (a) Henrissat, B. Biochem J 1991, 280, 309. (b) Henrissat, B.; Bairoch, A. Biochem J 1993, 293, 781.
52. (a) Li, Y. K.; Chir, J.; Tanaka, S.; Chen. F. Y. Biochemistry 2002, 41, 2751. (b) Henrissat, B. Biochem. J. 1991, 280, 309. (c) Henrissat, B.; Davies, G. Curr. Opin. Struct. Biol. 1997, 7, 637.
53. Gebler, J. C.; Gilkes, N. R.; Claeyssens, M.; Wilson, D. B.; Beguin, P.; Wakarchuk, W.; Kilburn, D. G.; Miller, R. C. Jr.; Warren, R. A.; Withers, S. G. J Biol Chem 1992, 267, 12259.
54. Koshland, D. E. Biol Rev 1953, 28, 416.
55. Rouvinen, J.; Bergfors, T.; Teeri, T.; Knowles, J. K. C.; Jones, T. A. Science 1990, 249, 380.
56. Spezio, M.; Wilson, D. B.; Karplus, P. A. Biochemistry 1993, 32, 9906.
57. Mikami, B.; Hehre, E. J.; Sato, M.; Katsube, Y.; Hirose, M.; Morita, Y.; Sacchettini, J. C. Biochemistry 1993, 32, 6836.
58. Aleshin, A.E.; Firsov, L. M.; Honzatko, R. B. J Biol Chem 1994, 269, 15631.
59. Matsui, H.; Blanchard, J. S.; Brewer, C.F.; Hehre, E. J. J Biol Chem 1989, 264, 8714.
60. van Doorslaer, E.; van Opstal, O.; Kersters-Hilderson, H.; De Bruyne, C. K. Bioorg Chem 1984, 12, 158.
61. Liu, W.; Madsen, N. B.; Braun, C.; Withers, S. G. Biochemistry 1991, 30, 1419.
62. Phillips, D. C. Proc. Natl. Acad. Sci. USA 1967, 57, 484.
63. (a) Qian, M.; Haser, R.; Payan, F. J. Mol. Biol. 1993, 231, 785. (b) Larson, S. B.; Greenwood, A.; Cascio, D.; Day, J.; McPherson, A. J. Mol. Biol.1994, 235, 1560.
64. Klein, C.; Hollender, J.; Bender, H.; Schulz, G. E. Biochemistry 1992, 31, 8740.
65. Wakarchuk, W. W.; Campbell, R. L.; Sung, W. L.; Davoodi, J.; Yaguchi, M. Protein Sci 1994, 3, 467.
66. Tanaka, K. S. E.; Winters, G. C.; Batchelor, R. J.; Einstein, F. W. B.; Bennet, A. J. J. Am. Chem. Soc. 2001, 123, 998.
67. Withers, S. G.; Aebersold, R. Protein Science 1995, 4, 361.
68. (a) Pauling, L. Chem. Eng. News 1946, 1375. (b) Schröder, P. N.; Giannis, A. Angew. Chem. Int. Ed. Engl. 1999, 38, 1379.
69. (a) Koshland, D. E. Jr. Biol. Rev. 1953, 28, 416. (b) Withers, S. G.; Street, I. P. J. Am. Chem. Soc. 1988, 110, 8551. (c) Sinnott, M. L. Chem. Rev. 1990, 90, 1171. (d) Legler, G. Adv. Carbohydr. Chem. Biochem. 1990, 48, 319. (e) McCarter, J. D.; Withers, S. G. Curr. Opin. Struct. Biol. 1994, 4, 885. (f) Withers, S. G. Pure Appl. Chem. 1995, 67, 1673. (g) Huang, X.; Tanaka, K. S. E.; Bennet, A. J. J. Am. Chem. Soc. 1997, 119, 11147. (h) Zechel, D. L.; Withers, S. G. Acc. Chem. Res. 2000, 33, 11.
70. Strynadka, N. C. J.; James, M. N. G. J. Mol. Biol. 1991, 220, 401.
71. (a) Asano, N.; Nishida, M.; Kato, A.; Kizu, H.; Matsui, K.; Shimada, Y.; Itoh, T.; Baba, M.; Watson, A. A.; Nash, R. J.; de Q. Lilley, P. M.; Watkin, D. J.; Fleet, G. W. J. J. Med. Chem. 1998, 41, 2565. (b) Oki. T.; Matsui, T.; Osajima, Y. J. Agric. Food Chem. 1999, 47, 550.
72. Inouye, S.; Tsuruoka, T.; Niida, T. J. Antibiot. 1966, 19, 288.
73. Jespersen, T. M.; Dong, W.; Sierks, M. R.; Skrydstrup, T.; Lundt, I.; Bols, M. Angew. Chem. Int. Ed. Engl. 1994, 41, 2565.
74. Kameda, Y.; Horii, S. J. Chem. Soc., Chem. Commun. 1972, 746.
75. Ermert, P.; Vasella, A. Helv. Chim. Acta 1991, 74, 2043.
76. Henrissat, B.; Czjzek, M.; Darbon, H.; Mosbah, A.; Receveur, V.; Roig-Zamboni, V. AFMB Activity Report 1996-1999 1999, 47.
77. Le, V. D.; Wong, C. H. J. Org. Chem. 2000, 65, 2399.
78. Capon, B. Chem. Rev. 1969, 69, 407.
79. (a) Bousquet, E.; Spadaro, A.; Pappalardo, M. S.; Bernardini, R.; Romeo, R.; Panza, L.; Ronsisvalle, G. J. Carbohydr. Chem. 2000, 19, 527. (b) Rich, J. R.; Bundle, D. R. Org. Lett. 2004, 6, 897. (c) Kuberan, B.; Sikkander, S. A.; Tomiyama, H.; Linhardt, R. J. Angew. Chem. 2003, 115, 2119; Angew. Chem. Int. Ed. 2003, 42, 2073.
80. Wallenfels, K.; Malhotra, O. P. Adv. Carbohydr. Chem. 1961, 16, 239.
81. Driguez, H. Top. Curr. Chem. 1997, 187, 85.
82. Nicotra, F. Top. Curr. Chem. 1997, 187, 55.
83. Czjzek, M.; Cicek, M.; Zamboni, V.; Burmeister, W. P.; Bevan, D. R.; Henrissat, B.; Eswn, A. Biochem. J. 2001, 354, 37.
84. Naider, F.; Bohak, Z.; Yariv, J. Biochemistry 1972, 11, 3202.
85. Legler, G. Adv Carbohydr Chem Biochem 1990, 48, 319.
86. Black, T.; Kiss, L.; Tull, D.; Withers, S. G. Carbohydr. Res. 1993, 250, 195.
87. Shulman, M. L.; Shiyan, S. D.; Khorlin, A. Y. Biochim Biophys Acta 1976, 445, 169.
88. Bause, E.; Legler, G. Hoppe-Seyler’s Z Physiol Chem 1974, 355, 438.
89. Legler, G.; Bause, E. Carbohydr. Res. 1973, 28, 45.
90. Clarke, A. J.; Strating, H. Carbohydr. Res. 1989, 188, 245.
91. Bordier, H. P.; Rodriguez, E. B.; lsre, J.; Stick, R. V.; Stone, B. A. J. Biol. Chem. 1991, 266, 11628.
92. Macarron, R.; van Beeumen, J.; Henrissat, B.; de la Mata, 1.; Claeyssens, M. Trichoderma. reesei. FEES Lett. 1993, 316, 137.
93. Keitel, T.; Simon, O.; Borriss, R.; Heinemann, U. Proc. Nut1. Acad. Sci. USA 1993, 90, 5287.
94. (a) Stick, R. V.; Høj, P. B.; Rodriguez, E. B.; Stone, B. A. J. Biol. Chem. 1989, 264, 4939. (b) Stick, R. V.; Rodriguez, E. B. Aust. J. Chem. 1990, 43, 665. (c) Stick, R. V.; Rodriguez, E. B.; Scally, G. D. Aust. J. Chem. 1990, 43, 1391. (d) Stick, R. V.; Høj, P. B.; Rodriguez, E. B.; Iser, J. R.; Stone, B. A. J. Biol. Chem. 1991, 266, 11628. (e) Høj, P. B.; Condron, R.; Traeger, J. C.; McAuliffe, J.C.; Stone, B. A. J. Biol. Chem. 1992, 267, 25059. (f) Szurmai, Z.; Kerékgyártó, J.; Nagy, Z. Carbohydr. Res. 1997, 297, 107. (g) Peräkylä, M.; Laitinen, T.; Rouvinen, J. J. Org. Chem. 1998, 63, 8157. (h) Stick, R. V.; Fairweather, J. K.; Tilbrook, D. M. G. Aust. J. Chem. 1998, 51, 471. (i) Stick, R. V.; Fairweather, J. K.; Tilbrook, D. M. G.; Driguez, H. Tetrahedron 1999, 55, 3695. (j) Stick, R. V.; Fairweather, J. K.; Withers, S. G. Aust. J. Chem. 2000, 53, 913.
95. (a) Legler, G. Adv. Carbohydr. Chem. Biochem. 1990, 48, 319. (b) Kanfer, J. N.; Stephens, M. C.; Singh, H.; Legler, G. Prog. Clin. Biol. Res. 1982, 95, 627.
96. Withers, S. G.; Umezawa, K. Biochem. Biophys. Res. Commun. 1991, 177, 532.
97. Atsumi, S.; Nosaka, C.; Iinuma, H.; Umezawa, K. Arch. Biochem. Biophys. 1992, 297, 362.
98. (a) Sinnott, M. L.; Smith, P. J. J. Chem. Soc., Chem. Commun. 1976, 6, 223. (b) Marshall, P. J.; Sinnott, M. L.; Smith, P. J.; Widdows, D. J. Chem. Soc. Perkin. Trans.1981, 2, 366.
99. (a) Fowler, A. V.; Zabin, I.; Sinnott, M. L.; Smith, P. J. J. Biol. Chem. 1978, 253, 5283. (b) Fowler, A. V.; Smith, P. J. J. Biol. Chem. 1983, 258, 10204.
100. Halazy, S.; Danzin, C.; Ehrhard, A.; Gerhart, F. J. Am. Chem. Soc. 1989, 111, 3484.
101. Halazy, S.; Berges, V.; Ehrhard, E.; Danzin, C. Bioorg. Chem. 1990, 18, 330.
102. (a) Palo, R. T. J. Chem. Ecol. 1984, 10, 499. (b) Clausen, T.P.; Keller, J. W.; Reichardt, P. B. Tetrahedron Lett. 1990, 31, 4537.
103. Zhu, J.; Withers, S. G.; Reichardt, P. B.; Treadwell, E.; Clavsen, T. P. Biochem. J. 1998, 332, 367.
104. (a) Withers, S. G.; Street, I. P.; Bird, P.; Dolphin, D. H. J. Am. Chem. Soc.1987, 109, 7530. (b) Withers, S. G.; Rupitz, K.; Street, I. P. J. Biol. Chem.1988, 263, 7929.
105. McCarter, J.; Adam, M.; Withers, S. G. Biochem. J.1992, 286, 721.
106. (a) Lo, L.-C.; Pang, T.-L.; Kuo, C.-H.; Chiang, Y.-L.; Wang, H.-T; Lin, J.-J. J. Proteome Res. 2002, 1, 35. (b) Lo, L.-C; Lo, C.-H. L.; Janda, K. D. Bioorg. Med. Chem. Lett. 1996, 6, 2117. (c) Janda, K. D.; Lo, L.-C.; Lo, C.-H. L.; Sim, M.-M.; Wang, R.; Wong, C.-H.; Lerner, R. A. Science 1997, 275, 945. (d) Hermetter, A.; Scholze, H.; Stutz, A. E.; Withers, S. G.; Wrodnigg, T. M. Bioorg. Med. Chem. Lett. 2001, 11, 1339. (e) Betley, J. R.; Tadic, S. C.; Mekhafia, A.; Rickard, J. H.; Denham, H.; Partridge, L. J.; Plückthun, A.; Blackburn, G. M. Angew. Chem. Int. Ed. 2002, 41, 775.
107. (a) Tsai, C.-S.; Li, Y.-K.; Lo, L.-C. Org. Lett. 2002, 4, 3607. (b) Kurogochi, M.; Nishimura, S.-I.; Lee, Y. C. J. Biol. Chem. 2004, 279, 44704.
108. Hinou, H.; Kurogochi, M.; Shimizu, H.; Nishimura, S.-I. Biochemistry 2005, 44, 11669.
109. Komatsu, T.; Kikuchi, K.; Takakusa, H.; Hanaoka, K.; Ueno, T.; Kamiya, M.; Urano, Y.; Nagano, T. J. Am. Chem. Soc. 2006, 128, 15946.
110. Wicki, J.; Rose, D. R.; Withers, S. G. Methods Enzymol. 2002, 354, 84.
111. (a) Vocadlo, D. J.; Davies, G. J.; Laine, R.; Withers, S. G. Nature 2001, 412, 835. (b) Vocadlo, D. J.; Withers, S. G. Methods Mol. Biol. 2000, 146, 203. (c) Withers, S. G.; Rupitz, K.; Street, I. P. J. Biol. Chem. 1988, 263, 7929.
112. Vocadlo, D. J.; Bertozzi, C. R. Angew. Chem. Int. Ed. 2004, 43, 5338.
113. Speers, A. E.; Cravatt, B. F. ChemBioChem, 2004, 5, 41.
114. Zechel, D. L.; Withers, S. G. Acc. Chem. Res. 2000, 33, 11.
115. Withers, S. G.; Williams, S. J.; Hekmat, O. ChemBioChem 2006, 7, 116.
116. Esen, A. β-Glucosidases, Biochemistry and Molecular Biology 1992.
117. Sue, M.;Ishihara, A.; Iwamura, H. Planta 2000, 210, 432.
118. Sinnott, M. L. Chem. Rev. 1990, 90, 1171.
119. (a) Grover, A. K.; Macmurchie, D. D.; Gushley, R. J. Biochimica et Biophysica Acta. 1977, 482, 98. (b) Legler, G.; Harder, A. Biochimica et Biophysica Acta. 1978, 524, 102.
120. He, S.; Withers, S. G. J. Biol. Chem. 1997, 272, 24864.
121. Graham, T. Philos. Trans. R. Soc. 1861, 151, 183.
122. Daniel, M. C.; Astruc, D. Chem. Rev. 2004, 104, 293.
123. (a) Brus, L. E.; Efros, A. L.; Itoh, T. J. Lumin. 1996, 70, R7. (b) Weller, H. Philo. Trans. R. Soc. London, Ser. A 1996, 354, 757.
124. Stepanyuk, V. S.; Hergert, W.; Rennert, P.; Wildberger, K.; Zeller, R.; Dederichs, P. H. Surf. Sci. 1997, 377, 495.
125. Kalyanasundaram, K.; Borgarello, E.; Duonghong, D.; Gratzel, M. Angew. Chem. Int. Ed. Engl. 1981, 20, 933.
126. Brust, M.; Kiely, C. J. Colloids Surf. A: Physicochem. Eng. Asp. 2002, 202, 175.
127. (a) Bohren, C. F.; Huffman, D. R. Absorption and Scattering of Light by Small Particles John Wiley & Sons: New York, 1983. (b) Logunov, S. L.; Ahmadi, T. S.; Elsayed, M. A.; Khoury, J. T.; Whetten, R. L. J. Phys. Chem. B 1997, 101, 3713. (c) Zaitoun, M. A.; Mason, W. R.; Lin, C. T. J. Phys. Chem. B 2001, 105, 6780. (d) Melinger, J. S.; Kleiman, V. D.; McMorrow, D.; Grőhn, F.; Bauer, B. J.; Amis, E. J. Phys. Chem. A 2003, 107, 3424. (e) Papavassiliou, G. C. Prog. Solid State Chem. 1979, 12, 185.
128. (a) Storhoff, J. J.; Lazarides, A. A.; Mucic, R. C.; Mirkin, C. C.; Letsinger, R. L.; Schatz, G. C. J. Am. Chem. Soc. 2000, 122, 4640. (b) Alvarez, M. M.; Khoury, J. T.; Schaaff, T. G.; Shafigullin, M. N.; Vezmar, I.; Whetten, R. L. J. Phys. Chem. B. 1997, 101, 3706.
129. Whiteside, G. M.; Grzybowski, B. Science , 2002, 295, 2418.
130. (a) Zayats, M.; Kharitonov, A. B.; Pogorelova, S. P.; Lioubashevski, O.; Katz, E.; Willner, I. J. Am. Chem. Soc. 2003, 125, 16006. (b) Willner, I.; Willner, B. Pure. Appl. Chem. 2002, 74, 1773.
131. (a) Zhong, C. J.; Maye, M. M. Adv. Mater. 2001, 13, 1507. (b) Mohr, C.; Hofmeister, H.; Radnik, J.; Claus, P. J. Am. Chem. Soc. 2003, 125, 1905.
132. (a) Berven, C. A.; Clark, L.; Mooster, J. L.; Wybourne, M. N.; Hutchison, J. E. Adv. Mater. 2001, 13, 109. (b) Sone, J.; Fujita, J.; Ochiai, Y.; Manako, S.; Matsui, S.; Nomura, E.; Baba, T.; Kawaura, H.; Sakamoto, T.; Chen, C. D.; Nakamura, Y.; Tsai, J. S. Nano- technology 1999, 10, 135. (c) Maier, S. A.; Brongersma, M. L.; Kik, P. G.; Meltzer, S.; Requicha, A. A. G.; Koel, B. E.; Atwater, H. A. Adv. Mater. 2001, 13, 1501.
133. (a) Brust, M.; Walker, M.; Bethell, D.; Schiffrin, D. J.; Whyman, R. J. J. Chem. Soc., Chem. Commun. 1994, 801. (b) Brust, M.; Fink, J.; Bethell, D.; Schiffrin, D. J.; Kiely, C. J. J. Chem. Soc., Chem. Commun. 1995, 1655.
134. Hayat, M. A. Colloidal Gold, Principles, Methods and Applications, Academic Press: New York, 1989.
135. Frens, G. Nature: Phys. Sci. 1973, 241, 20.
136. 葉儒林,金奈米粒子之合成機制及其應用研究,2002年8月。
137. Niemeyer, C. M. Angew. Chem., Int. Ed. 2001, 40, 4128.
138. (a) Mirkin, C. A.; Letsinger, R. L.; Mucic, R. C.; Storhoff, J. J. Nature 1996, 382, 607. (b) Elghanian, R.; Storhoff, J. J.; Mucic, R. C.; Letsinger, R. L.; Mirkin, C. C. Science, 1997, 277, 1078.
139. Otsuka, H.; Akiyama, Y.; Nagasaki, Y.; Kataoka, K. J. Am. Chem. Soc., 2001, 123, 8226.
140. (a) Hone, D. C.; Haines, A. H.; Russell, D. Langmuir, 2003, 19, 7141. (b) Fuente, J. M. de la ; Penadés, S. Biochimica et Biophysica Acta 2006, 636. (c) Chen, C.-T.; Tsai, C.-S.; Yu, T.-B. Chem. Commun. 2005, 4273.
141. Lin, C.-C.; Yeh, Y.-C.; Yang, C.-Y.; Chen, C.-L.; Chen, G.-F.; Chen, C.-C., Wu, Y.-C. J. Am. Chem. Soc., 2002, 124, 3508.
142. Chen, G.; Heim, A.; Riether, D.; Yee, D.; Milgrom, Y.; Gawinowicz, M. A.; Sames, D. J. Am. Chem. Soc. 2003, 125, 8130.
143. (a) Thomas, E. W.; McKelvey, J. F.; Sharon, N. Nature 1969, 222, 485. (b) O’Connell, E. L.; Rose, I. A. J. Biol. Chem. 1973, 248, 2225. (c) Greenbaum, D.; Medzihradszky, K. F.; Burlingame, A.; Bogyo, M. Chem. Biol. 2000, 7, 569. (d) Groll, M.; Kim, K. B.; Kairies, N.; Huber, R.; Crews, C. M. J. Am. Chem. Soc. 2000, 122, 1237. (e) Abad, J. M.; Vélez, M.; Santamaría, C.; Guisán, M.; Matheus, P. R.; Vázquez, L.; Gazaryan, I.; Gorton, L.; Gibson, T.; Fernández, V. M. J. Am. Chem. Soc. 2002, 124, 12845. (f) Comens, P. G.; Simmer, R. L.; Baker, J. B. J. Biol. Chem. 1982, 257, 42. (g) Gartner, Z. J.; Liu, D. R. J. Am. Chem. Soc. 2001, 123, 6961.
144. 國立臺灣大學理學院化學研究所博士論文 蔡長昇撰 2006.7
145. Schlüter, A. D.; Zistler, A.; Koch, S. J. Chem. Soc., Perkin Trans. 1 1999, 501.
146. Stoddart, J. F.; Fulton, D. A.; Pease, A. R. Isr. J. Chem. 2000, 40, 325.
147. Stoddart, J. F.; Meijer, E. W.; Ashton, P. R.; Boyd, S. E.; Brown, C. L.; Nepogodiev, S. A.; Peerlings, H. W. I. Chem. Eur. J. 1997, 3, 974.
148. Kihlberg, J.; Elofsson, M.; Walse, B. Tetrahedron Lett. 1991, 32, 7613.
149. Magnusson, G.; Wilstermann, M.; Kononov, L. O.; Nilsson, U.; Ray, A. K. J. Am. Chem. Soc. 1995, 117, 4742.
150. Kunz, H.; Kallus, C.; Opatz, T.; Wunberg, T.; Schmidt, W.; Henke, S. Tetrahedron Lett. 1999, 40, 7783.
151. (a) Rzeszotarska, B.; Wiejak, S.; Masiukiewicz, E. Chem. Pharm. Bull. 1999, 47, 1489-1490. (b) Pombo-Villar, E.; Watts, P.; Wiles, C.; Haswell, S. J. Tetrahedron 2002, 58, 5427.
152. (a) Martinez, J.; Rodriguez, M.; Llinares, M.; Doulut, S.; Heitz, A. Tetrahedron Lett. 1991, 32, 923. (b) Kokotos, G. Synthesis, 1990, 299. (c) Palumbo, G.; Caputo, R.; Cassano, E.; Longobardo, L. Tetrahedron Lett. 1995, 36, 167. (d) Grieco, P.; Campiglia, P.; Gomez-Monterrey, I.; Longobardo, L.; Lama, T.; Novellino, E. Tetrahedron Lett. 2004, 45, 1453. (e) Giovanni, P.; Caputo, R.; Cassano, E.; Longobardo, L. Tetrahedron 1995, 51, 12337.
153. Guillerm, D.; Lavrador, K.; Guillerm, G. Synth. Commun. 1995, 25, 877.
154. Huang, L.; Olmstead, M. M.; Kurth, M. J. Org. Prep. Poced. Int. 2002, 34, 521.
155. Nudelman, A.; Nudelman, A.; Bechor, Y.; Falb, E.; Fischer, B.; Wexler, B. A. Synth. Commun. 1998, 28, 471.
156. (a) Singh, A.; Thornton, E. R.; Westheimer, F. H. J. Biol. Chem. 1962, 237, 3006. (b) Goeldner, M.; Kotzyba-Hibert, F.; Kapfer, I. Angew. Chem. Int. Ed. Engl. 1995, 34, 1296. (c) Völkert, M.; Uwai, K.; Tebbe, A.; Popkirova, B.; Wagner, M.; Kuhlmann, J.; Waldmann, H. J. Am. Chem. Soc. 2003, 125, 12749. (d) Hermann Dugas (1996), Bioorganic Chemistry: a Chemical Approach to Enzyme Action, 3rd. Ed., Chap. 7, pp.543., Spring-Verlag, New York. (e) Richard P. Haugland, Handbook of Fluorescent Probes and Research products, 9th. Ed., Chap. 5, pp.144., Molecular Probes. (f) Lin, S.; Fang, K.; Hashimoto, M.; Nakanishi, K.; Ojima, I. Tetrahedron Lett. 2000, 41, 4287. (g) Fleming, S. A. Tetrahedron 1995, 51, 12479. (h) Fleming, S. A. Tetrahedron 1995, 51, 12479. (i) Dormán, G.; Prestwich, G. D. Trends. Biotechnol. 2000, 18, 64. (j) Hatanaka, Y.; Sadakane, Y. Curr. Top. Med. Chem. 2002, 2, 271.
157. (a) Yamamoto, N.; Bernardi, F.; Olivucci, M.; Robb, M. A.; Wilsey, S. J. Am. Chem. Soc. 1994, 116, 2064. (b) Fleet, G. W. J.; Porter, R. R.; Knowles, J. R. Nature 1969, 224, 511. (c) Kemnitz, C. R.; Karney, W. L.; Borden, W. T. J. Am. Chem. Soc. 1998, 120, 3499. (d) Platz, M. S. Acc. Chem. Res. 1995, 28, 487. (e) Karney, W. L.; Borden, W. T. J. Am. Chem. Soc. 1997, 119, 3347. (f) Chehade, K. A. H.; Spielmann, H. P. J. Org. Chem. 2000, 65, 49493. (g) Brown, R. L.; Gerber, W. V.; Karpen, J. W. Proc. Natl. Acad. Sci. USA 1993, 90, 5369. (h) Resek, J. F.; Ruoho, A. E. J. Biol. Chem. 1988, 263, 14410. (i) Brunner, J.; Senn, H.; Richards, F. J. Biol. Chem. 1980, 255, 3313. (j) Hatanaka. Y.; Yoshida, E.; Nakayama, H. et al. Bioorg. Chem. 1989, 17, 482. (k) Nassal, M. J. Am. Chem. Soc. 1984, 106, 7540. (l) Dormán, G.; Prestwish, G. D. Biochemistry 1994, 33, 5661. (m) Prestwich, G. D.; Dorman, G.; Elliott, J. T. et al. Photochem Photobiol 1997, 65, 222. (n) Weber, P. J. A.; Beck-Sickinger, A. G. J. J. Peptide. Res. 1997, 49, 375.
158. (a) Jong-Jip, P.; Hatanaka, Y.; Kempin, U. J. Org. Chem. 2000, 65, 5639. (b) Hamachi, I.; Nagase, T.; Shinkai, S. J. Am. Chem. Soc. 2000, 122, 12065. (c) Hamachi, I.; Nakata, E.; Koshi, Y.; Koga, E.; Katayama, Y. J. Am. Chem. Soc. 2005, 127, 13253.
159. Shin, I.; Lee, M.-r.; Jung, D.-W.; Williams, D. Org. Lett. 2005, 7, 5477.
160. Suzuki, M.; Hosoya, T.; Hiramatsu, T.; Ikemoto, T.; Nakanishi, M.; Aoyama, H.; Hosoya, A.; Iwata, T.; Maruyama, K.; Endo, M. Org. Biomol. Chem. 2004, 2, 637.
161. Pieters, R. J.; Ballell, L.; Alink, K. J.; Slijper, M.; Versluis, C.; Liskamp, R. M. J. ChemBioChem 2005, 6, 291.
162. Belshaw, P. J.; Lamos, S. M.; Krusemark, C. J.; McGee, C. J.; Scalf, M.; Smith, L. M. Angew. Chem. Int. Ed. 2006, 45, 4329.
163. (a) 林敬二、楊美惠、楊寶旺、廖德章、薛敬和(1993),中英日化學大辭典,pp.170,高立圖書。(b) Richard P. Haugland, Handbook of Fluorescent Probes and Research products, 9th. Ed., Chap. 4, pp.121-134., Molecular Probes. (c) Richard P. Haugland, Handbook of Fluorescent Probes and Research products, 9th. Ed., Chap. 7, pp.254-257., Molecular Probes.
164. Speers, A. E.; Cravatt, B. F. ChemBioChem 2004, 5, 41.
165. (a) Kolb, H. C.; Sharpless, K. B. Drug Discov Today 2003, 8, 1128. (b) Cravatt, B. F.; Speers, A. E. Chem. Biol. 2004, 11, 535.
166. Kolb, H. C.; Finn, M. G.; Sharpless, K. B. Angew Chem Int Ed Engl 2001, 40, 2004.
167. Huisgen, R. Angew Chem Int Ed Engl 1963, 2, 565.
168. (a) Rostovtsev, V. V.; Green, J. G.; Fokin, V. V.; Sharpless, K. B. Angew. Chem., Int. Ed. 2002, 41, 2596. (b) Tornøe, C. W.; Christensen, C.; Meldal, M. J. Org. Chem. 2002, 67, 3057. (c) Li, Z.; Seo, T. S.; Ju, J. Tetrahedron Lett. 2004, 45, 3143.
169. (a) Saxon, E.; Bertozzi, C. R. Science 2000, 287, 2007. (b) Kiick, K. L.; Saxon, E.; Tirrell, D. A.; Bertozzi, C. R. Proc Natl Acad Sci USA 2002, 99, 19.
170. Prescher, J. A.; Bertozzi, C. R. Nat Chem Biol 2005, 1, 13.
171. Link, A. J.; Tirrell, D. A. J. Am. Chem. Soc. 2003, 125, 11164.
172. (a) Lewis, W. G.; Green, L. G.; Grynszpan, F.; Radić, Z.; Carlier, P. R.; Taylor, P.; Finn, M. G.; Sharpless, K. B. Angew. Chem. Int. Ed. 2002, 41, 1053. (b) Lee, L. V.; Mitchell, M. L.; Huang, S.-J.; Fokin, V. V.; Sharpless, K. B.; Wong, C.-H. J. Am. Chem. Soc. 2003, 125, 9588. (c) Srinivasan, R.; Uttamchandani, M.; Yao, S. Q. Org. Lett. 2006, 8, 713.
173. Fazio, F.; Bryan, M. C.; Blixt, O.; Paulson, J. C.; Wong, C.-H. J. Am. Chem. Soc. 2002, 124, 14397.
174. (a) Adam, G. C.; Cravatt, B. F.; Sorensen, E. J. Chem. Biol. 2001, 8, 81. (b) Adam, G. C.; Sorensen, E. J.; Cravatt, B. F. Nat. Biotechnol. 2002, 20, 805.
175. Cravatt, B. F.; Speers, A. E.; Adam, G. C. J. Am. Chem. Soc. 2003, 125, 4686.
176. (a) Stick, R. V.; Rodriguez, E. B.; Scally, G. D. Aust. J. Chem. 1990, 43, 1391. (b) Ferrier, R. J.; Hall, D. W. J. Chem. Soc. Perkin Trans. 1 1992, 3029.
177. (a) Vaultier, M.; Carboni, B.; Benalil, A. J. Org. Chem. 1993, 58, 3736. (b) Carboni, B.; Benalil, A.; Vaultier, M. Tetrahedron 1991, 47, 8177.
178. (a) Nilsson, U. J.; Billing, J. F. J. Org. Chem. 2005, 70, 4847. (b) Chu, L.; Hutchins, J. E.; Weber, A. E.; Lo, J.-L.; Yang, Y.-T.; Cheng, K.; Smith, R. G.; Fisher, M. H.; Wyvratt, M. J.; Goulet, M. T. Bioorg. Med. Chem. Lett. 2001, 11, 509. (c) Smith, P. W.; Sollis, S. L.; Howes, P. D.; Cherry, P. C.; Starkey, I. D.; Cobley, K. N.; Weston, H.; Scicinski, J.; Merritt, A.; Whittington, A.; Wyatt, P.; Taylor, N.; Green, D.; Bethell, R.; Madar, S.; Fenton, R. J.; Morley, P. J.; Pateman, T.; Beresford, A. J. Med. Chem. 1998, 41, 787.
179. Wong, C.-H.; Sawa, M.; Hsu, T.-L.; Itoh, T.; Sugiyama, M.; Hanson, S. R.; Vogt, P. K. Proc. Natl. Acad. Sci. USA 2006, 103, 12371.
180. Kodadek, T.; Alluri, P. G.; Reddy, M. M.; Bachhawat-Sikder, K.; Olivos, H. J. J. Am. Chem. Soc. 2003, 125, 13995.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/28966-
dc.description.abstract在生物體內,醣類衍生物被視為訊息攜帶分子,涉及免疫反應、病毒感染,以及細胞間的辨識與訊息傳遞等生物功能,其重要性使得醣質生物學(glycobiology)成為生命科學的新焦點。而醣苷水解酶在控制生物體內醣類的代謝、生成,以及細胞表面分子辨識上扮演了重要角色,若活性失調可能引起多種疾病。因此,這類酵素的研究將有助於臨床上疾病診斷與治療、藥物開發及病理瞭解等。在本論文中,是以商業上可購得來自杏仁的β-葡萄糖水解酶(β-glucosidase)為研究對象。並利用ABPP(activity-based protein profiling)策略發展其活性標示探針,以期能應用於蛋白質體學(proteomics)的研究上。我們成功發展了對β-葡萄糖水解酶具有標示潛力的光親合性(photoaffinity)活性標示探針B-1(為酵素表面標示的探針),以及以酵素催化機制為基礎的(mechanism-based)活性標示探針C-1(為酵素活性中心內標示的探針)。其中,探針B-1的設計包括了S-linked β-D-葡萄糖衍生物、光反應基團,以及生物素標籤。這三重功能性探針的設計是希望探針在與目標蛋白質專一辨識後,經由照光反應可以在活性中心附近形成共價鍵結,再由生物素的標籤輸出訊號。在探針B-1標示蛋白質的相關實驗中,已證實其能與目標酵素活性中心親合性結合,並以共價鍵連結。另外,探針C-1的設計包括了epoxyalkyl glucosides衍生物和疊氮(azido)基團。其設計是希望藉由酵素催化過程與探針上反應基團epoxide形成共價鍵結,再利用疊氮基團進行click反應連接標籤。而在標示蛋白質的相關實驗中,則發現缺乏epoxide的對照物C-1a標示效果較探針C-1佳,但目前仍未知其與酵素形成共價鍵的機制。此外,這些探針進行蛋白質標示的結果顯示配基為S-linked的探針B-1專一性較不高,而具有天然O-linked配基的探針C-1對β-葡萄糖水解酶具有專一性。最後,這些探針組裝式的合成提供了未來其結構改良的簡便性,可再經由配基或反應基團的置換等,來提升探針的專一性標示。zh_TW
dc.description.abstractIn organisms, saccharide derivatives are deemed as information carriers, involving biological functions, such as immune response, virus infection, cell-cell communication and signal transduction, etc.. Their biological importance makes glycobiology become a new focus of life sciences. Among them, glycosidases play important roles in controlling saccharide metabolism, anabolism and cell surface molecule recognization. Any imbalance in their activities may result in many kinds of diseases. So the study of this kind of enzymes will benefit to the clinical diagnosis/treatment, drug discovery and understanding pathology etc. In this thesis, the commercially available β-glucosidase from almonds is used as the research model. Various ABPs (activity-based probes) were developed to label the enzymes hoping to extend the strategy to study proteome. We have succeeded in developing photoaffinitity ABP B-1 (exo-labeling probes) and mechanism-based ABP C-1 (endo-labeling probes), which exhibit potential in labeling β-glucosidases. Probe B-1 consists of a S-linked β-D-glucose derivative, a photoreactive group, and a biotin tag. This trifunctional probe is designed to form the covalent bond by photoreacting group near the active site once the probe and the targeted protein were bound together specifically and the biotin tag could be regarded as output for facile purification. In the protein labeling experiment employing the probe B-1, it showed that the probe can recognize the active site of the targeted enzyme specifically via a covalent bond. The probe C-1 is composed of a epoxyalkyl glucoside derivative and an azido group. A covalent bond between the enzyme and epoxide reactive group forms first, and then an azido group could react with the tag by click reaction afterwards. The protein labeling experiment using control C-1a, which has no epoxide, displayed good labeling effect, despite that the labeling mechanism is not clear. Moreover, probe B-1, which has S-linked ligand, cannot specifically label β-glucosidases, whereas probe C-1, which has native O-linked ligand, can specifically label β-glucosidases. To summarize, the study has laid the foundation for the development of ABPP (activity-based protein profiling) probes. Moreover, the modules nature of the probe designs offer molecular simplicity and concision. The specificity can be improved either by changing the ligand or reactive groups.en
dc.description.provenanceMade available in DSpace on 2021-06-13T00:32:15Z (GMT). No. of bitstreams: 1
ntu-96-R94223031-1.pdf: 48548822 bytes, checksum: b30f2fcce41838987cd1232eb3199f46 (MD5)
Previous issue date: 2007
en
dc.description.tableofcontents目錄……………………………………………………………i
圖目錄………………………………………………………………iv
表目錄………………………………………………………………vii
簡稱用語對照表………………………………………………………viii
中文摘要……………………………………………………………xii
英文摘要………………………………………………………………………xiii
緒論…………………………………………………………………1
第一章 蛋白質體學之簡介
1.1 蛋白質體學之發展歷程…………………………………………………………6
1.1.1 蛋白質體學之定義與發展……………………………………6
1.1.2 傳統蛋白質化學與蛋白質體學研究之比較……………………7
1.2 基因體與蛋白質體之比較…………………………………………7
1.3 蛋白質體學之研究方法…………………………………………9
1.3.1 二維凝膠電泳法與質譜儀………………………………………10
1.3.2 化學蛋白質體學之ABPP方法………………………………11
第二章 醣苷水解酶之簡介
2.1 醣質生物學之簡介………………………………………………18
2.1.1 醣質生物學之發展歷程…………………………………………18
2.1.2 生物系統中醣類之功能…………………………………………19
2.1.3 醣類之結構特點…………………………………………………19
2.2 醣苷水解酶之重要……………………………………………………20
2.3 醣苷水解酶之作用機制……………………………………………22
2.3.1 醣苷水解酶之分類………………………………………………22
2.3.2 醣苷水解酶之催化機制………………………………………22
2.4 醣苷水解酶之抑制劑…………………………………………25
2.4.1 可逆抑制劑……………………………………………………25
2.4.2 不可逆抑制劑…………………………………………………27
2.5 醣苷水解酶之活性標示探針………………………………………33
2.6 目標酵素β-葡萄糖水解酶之簡介………………………………38
第三章 針對β-葡萄糖水解酶發展親合性活性標示探針
3.1 金奈米粒子之簡介…………………………………………………39
3.1.1 金奈米粒子之特性………………………………………………39
3.1.2 金奈米粒子之合成……………………………………………42
3.1.3 金奈米粒子應用於生物探針之簡介……………………44
3.2 親合性活性標示探針之設計與合成…………………………………………47
3.2.1 Dalibor Sames所發展具epoxide反應基團之親合性探針……47
3.2.2 親合性活性標示探針之設計………………………………….49
3.2.3 親合性活性標示探針之合成…………………………………51
3.3 結論……………………………………………………………62
第四章 針對β-葡萄糖水解酶發展光親合性活性標示探針
4-1 光親合性標示之簡介與應用………………………………………63
4.2 光親合性活性標示探針之設計與合成…………………………69
4.2.1 光親合性活性標示探針之設計…………………………………69
4.2.2 光親合性活性標示探針之合成………………………………71
4.3 結果與討論…………………………………………………………80
4.3.1 光親合性探針標示蛋白質之實驗流程…………………………80
4.3.2 光親合性探針標示蛋白質之結果分析………………………83
4.4 結論…………………………………………………89
第五章 針對β-葡萄糖水解酶發展以催化機制為基礎的活性標示探針
5.1 引入click化學的ABPP方法之簡介與應用………………………90
5.2 以酵素催化機制為基礎的活性標示探針之設計與合成…………94
5.2.1 以酵素催化機制為基礎的活性標示探針之設計………………94
5.2.2 以酵素催化機制為基礎的活性標示探針之合成………………97
5.3 結果與討論…………………………………………103
5.3.1 以酵素催化機制為基礎的探針標示蛋白質之實驗流程……103
5.3.2 以酵素催化機制為基礎的探針標示蛋白質之結果分析……105
5.4 結論………………………………………………………………121
第六章 總結…………………………………………………………122
實驗部分
壹、一般敘述……………………………………………123
貳、實驗步驟及光譜數據………………………………………125
參、生物活性測試方法……………………………………………165
參考文獻…………………………………………………174
附錄…………………………………………………………………193
dc.language.isozh-TW
dc.subjectβ-葡萄糖水解&#37238zh_TW
dc.subject蛋白質體學zh_TW
dc.subjectABPPzh_TW
dc.subject光親合性zh_TW
dc.subject以酵素催化機制為基礎的zh_TW
dc.subjectmechanism-baseden
dc.subjectβ-glucosidaseen
dc.subjectproteomicsen
dc.subjectABPPen
dc.subjectphotoaffinityen
dc.title針對β-葡萄糖水解酶發展酵素表面及活性中心內標示的兩種探針以應用於蛋白質體學研究zh_TW
dc.titleDeveloping exo- versus endo-Labeling Probes for β-Glucosidase Towards the Application in Proteomicsen
dc.typeThesis
dc.date.schoolyear95-2
dc.description.degree碩士
dc.contributor.oralexamcommittee鄭建中(Chien-Chung Cheng),羅禮強(Lee-Chiang Lo),劉緒宗(Shiuh-Tzung Liu)
dc.subject.keywordβ-葡萄糖水解&#37238,蛋白質體學,ABPP,光親合性,以酵素催化機制為基礎的,zh_TW
dc.subject.keywordβ-glucosidase,proteomics,ABPP,photoaffinity,mechanism-based,en
dc.relation.page245
dc.rights.note有償授權
dc.date.accepted2007-07-26
dc.contributor.author-college理學院zh_TW
dc.contributor.author-dept化學研究所zh_TW
顯示於系所單位:化學系

文件中的檔案:
檔案 大小格式 
ntu-96-1.pdf
  未授權公開取用
47.41 MBAdobe PDF
顯示文件簡單紀錄


系統中的文件,除了特別指名其著作權條款之外,均受到著作權保護,並且保留所有的權利。

社群連結
聯絡資訊
10617臺北市大安區羅斯福路四段1號
No.1 Sec.4, Roosevelt Rd., Taipei, Taiwan, R.O.C. 106
Tel: (02)33662353
Email: ntuetds@ntu.edu.tw
意見箱
相關連結
館藏目錄
國內圖書館整合查詢 MetaCat
臺大學術典藏 NTU Scholars
臺大圖書館數位典藏館
本站聲明
© NTU Library All Rights Reserved