메뉴 건너뛰기




Volumn 48, Issue 1, 2003, Pages 1-5

Peptide segment ligation: A new method for synthesis of peptide and protein

Author keywords

[No Author keywords available]

Indexed keywords


EID: 33749821822     PISSN: 10016538     EISSN: 18619541     Source Type: Journal    
DOI: 10.1360/03tb9001     Document Type: Review
Times cited : (5)

References (27)
  • 3
    • 0024968835 scopus 로고
    • A general method for site-specific incorporation of unnatural amino acids into proteins
    • Noren, C. J., Anthony-Cahill, S. J., Griffith, M. C. et al., A general method for site-specific incorporation of unnatural amino acids into proteins, Science, 1989, 244(4901): 182.
    • (1989) Science , vol.244 , Issue.4901 , pp. 182
    • Noren, C.J.1    Anthony-Cahill, S.J.2    Griffith, M.C.3
  • 4
    • 0000473766 scopus 로고    scopus 로고
    • From the biopolymer PHB to biological investigations of unnatural beta- and gamma-peptides
    • Seebach, D., Albert, M., Arvidsson, P. I. et al., From the biopolymer PHB to biological investigations of unnatural beta- and gamma-peptides, Chimia, 2001, 55(4): 345.
    • (2001) Chimia , vol.55 , Issue.4 , pp. 345
    • Seebach, D.1    Albert, M.2    Arvidsson, P.I.3
  • 5
    • 0027947767 scopus 로고
    • Synthesis of peptide dendrimer
    • Rao, C., Tam, J. P., Synthesis of peptide dendrimer, J. Am. Chem, Soc., 1994, 116(15): 6975.
    • (1994) J. Am. Chem, Soc. , vol.116 , Issue.15 , pp. 6975
    • Rao, C.1    Tam, J.P.2
  • 6
    • 0033402340 scopus 로고    scopus 로고
    • Chemical synthesis of proteins in solution
    • Sakakibara, S., Chemical synthesis of proteins in solution. Biopolymers (Peptide Sci.), 1999, 51(4): 279.
    • (1999) Biopolymers (Peptide Sci.) , vol.51 , Issue.4 , pp. 279
    • Sakakibara, S.1
  • 7
    • 0035685801 scopus 로고    scopus 로고
    • Methods and strategies of peptide ligation
    • Tam, J. P., Xu, J. X., Eom, K. D., Methods and strategies of peptide ligation, Biopolymers (Peptide Sci.), 2001, 60(3): 194.
    • (2001) Biopolymers (Peptide Sci.) , vol.60 , Issue.3 , pp. 194
    • Tam, J.P.1    Xu, J.X.2    Eom, K.D.3
  • 8
    • 0027944205 scopus 로고
    • Synthesis of protein by native chemical ligation
    • Dawson, P. E., Muir, T. W., Clark-Lewis, I. et al., Synthesis of protein by native chemical ligation, Science, 1994, 266(5186): 776.
    • (1994) Science , vol.266 , Issue.5186 , pp. 776
    • Dawson, P.E.1    Muir, T.W.2    Clark-Lewis, I.3
  • 9
    • 0033596308 scopus 로고    scopus 로고
    • Fmoc-hased synthesis of peptide-(alpha)thioesters: Application to the total chemical synthesis of a glycoprotein by native chemical ligation
    • Shin, Y., Winans, K. A., Backes, B. J. et al., Fmoc-hased synthesis of peptide-(alpha)thioesters: application to the total chemical synthesis of a glycoprotein by native chemical ligation. J. Am. Chem. Soc., 1999, 121(50): 11684.
    • (1999) J. Am. Chem. Soc. , vol.121 , Issue.50 , pp. 11684
    • Shin, Y.1    Winans, K.A.2    Backes, B.J.3
  • 10
    • 0033549108 scopus 로고    scopus 로고
    • Thia zip reaction for synthesis of large cyclic peptides: Mechanisms and applications
    • Tam, J. P., Lu, Y., Yu, Q., Thia zip reaction for synthesis of large cyclic peptides: mechanisms and applications, J. Am. Chem. Soc., 1999, 121(18): 4316.
    • (1999) J. Am. Chem. Soc. , vol.121 , Issue.18 , pp. 4316
    • Tam, J.P.1    Lu, Y.2    Yu, Q.3
  • 11
    • 0034995886 scopus 로고    scopus 로고
    • Selenocysteine-mediated native chemical ligation
    • Quaderer, R., Sewing, S., Hilvert, D., Selenocysteine-mediated native chemical ligation, Helv. Chim. Acta., 2001, 84(5): 1197.
    • (2001) Helv. Chim. Acta. , vol.84 , Issue.5 , pp. 1197
    • Quaderer, R.1    Sewing, S.2    Hilvert, D.3
  • 12
    • 0034808792 scopus 로고    scopus 로고
    • Selenocysteine in native chemical ligation and expressed protein ligation
    • Hondal, R. J., Nilsson, B. L., Raines, R. T., Selenocysteine in native chemical ligation and expressed protein ligation, J. Am. Chem. Soc., 2001, 123(21): 5140.
    • (2001) J. Am. Chem. Soc. , vol.123 , Issue.21 , pp. 5140
    • Hondal, R.J.1    Nilsson, B.L.2    Raines, R.T.3
  • 13
    • 0032189519 scopus 로고    scopus 로고
    • Methionine ligation strategy in the biomimetic synthesis of parathyroid hormones
    • Tam, J. P., Yu, Q., Methionine ligation strategy in the biomimetic synthesis of parathyroid hormones, Biopolymers (Peptide Sci.), 1998, 46(5): 319.
    • (1998) Biopolymers (Peptide Sci.) , vol.46 , Issue.5 , pp. 319
    • Tam, J.P.1    Yu, Q.2
  • 14
    • 0031013619 scopus 로고    scopus 로고
    • Orthogonal coupling of unprotected peptide segments through histidyl amino terminus
    • Zhang, L., Tam, J. P., Orthogonal coupling of unprotected peptide segments through histidyl amino terminus. Tetrahedron Lett., 1997, 38(1): 3.
    • (1997) Tetrahedron Lett. , vol.38 , Issue.1 , pp. 3
    • Zhang, L.1    Tam, J.P.2
  • 15
    • 0030037155 scopus 로고    scopus 로고
    • Extending the applicability of native chemical ligation
    • Canne, L. E., Bark, S. J., Kent, S. B. H., Extending the applicability of native chemical ligation, J. Am. Chem. Soc., 1996, 118(25): 5891.
    • (1996) J. Am. Chem. Soc. , vol.118 , Issue.25 , pp. 5891
    • Canne, L.E.1    Bark, S.J.2    Kent, S.B.H.3
  • 16
    • 0035804493 scopus 로고    scopus 로고
    • Native chemical ligation using removable N-alpha-(1-phenyl-2- mercaptoethyl)auxiliaries
    • Botti, P., Carrasco, M. R., Kent, S. B. H., Native chemical ligation using removable N-alpha-(1-phenyl-2-mercaptoethyl)auxiliaries, Tetrahedron Lett., 2001, 42(10): 1831.
    • (2001) Tetrahedron Lett. , vol.42 , Issue.10 , pp. 1831
    • Botti, P.1    Carrasco, M.R.2    Kent, S.B.H.3
  • 17
    • 0035811061 scopus 로고    scopus 로고
    • Total synthesis of cytochrome b562 by native chemical ligation using a removable auxiliary
    • Low, D. W., Hill, M. G., Carraso, M. R. et al., Total synthesis of cytochrome b562 by native chemical ligation using a removable auxiliary, Proc. Natl. Acad. Sci. USA, 2001, 98(12): 6554.
    • (2001) Proc. Natl. Acad. Sci. USA , vol.98 , Issue.12 , pp. 6554
    • Low, D.W.1    Hill, M.G.2    Carraso, M.R.3
  • 18
    • 0035977638 scopus 로고    scopus 로고
    • Synthesis of peptides and proteins without cycteine residues by native chemical ligation combined with desulfurization
    • Yan, L. Z., Dawson, P. E., Synthesis of peptides and proteins without cycteine residues by native chemical ligation combined with desulfurization, J. Am. Chem. Soc., 2001, 123(4): 526.
    • (2001) J. Am. Chem. Soc. , vol.123 , Issue.4 , pp. 526
    • Yan, L.Z.1    Dawson, P.E.2
  • 19
    • 12044253737 scopus 로고
    • Chemical ligation approach to form a peptide-bond between unprotected peptide segments-concept and model study
    • Liu, C. F., Tam, J. P., Chemical ligation approach to form a peptide-bond between unprotected peptide segments-concept and model study, J. Am. Chem. Soc., 1994, 116(10): 4149.
    • (1994) J. Am. Chem. Soc. , vol.116 , Issue.10 , pp. 4149
    • Liu, C.F.1    Tam, J.P.2
  • 20
    • 0028223433 scopus 로고
    • Peptide segment ligation strategy without use of protecting groups
    • Liu, C. F., Tam, J. P., Peptide segment ligation strategy without use of protecting groups, Proc. Natl. Acad. Sci. USA, 1994, 91(14): 6584.
    • (1994) Proc. Natl. Acad. Sci. USA , vol.91 , Issue.14 , pp. 6584
    • Liu, C.F.1    Tam, J.P.2
  • 21
    • 0032850010 scopus 로고    scopus 로고
    • Stereospecific pseudoproline ligation of N-terminal serine, threonine, or cycteine-containing unprotected peptides
    • Tam, J. P., Miao, Z., Stereospecific pseudoproline ligation of N-terminal serine, threonine, or cycteine-containing unprotected peptides, J. Am. Chem. Soc., 1999, 121(39): 9013.
    • (1999) J. Am. Chem. Soc. , vol.121 , Issue.39 , pp. 9013
    • Tam, J.P.1    Miao, Z.2
  • 22
    • 0030053752 scopus 로고    scopus 로고
    • Orthogonal ligation of unprotected peptide segments through pseudoproline formation for the synthesis of HIV-1 protease
    • Liu, C. F., Rao, C., Tam, J. P., Orthogonal ligation of unprotected peptide segments through pseudoproline formation for the synthesis of HIV-1 protease, J. Am. Chem. Soc., 1996, 118(2): 307.
    • (1996) J. Am. Chem. Soc. , vol.118 , Issue.2 , pp. 307
    • Liu, C.F.1    Rao, C.2    Tam, J.P.3
  • 23
    • 0030711495 scopus 로고    scopus 로고
    • Protein synthesis by chemical ligation of unprotected peptides in aqueous solution
    • Muir, T. W., Dawson, P. E., Kent, S. B. H., Protein synthesis by chemical ligation of unprotected peptides in aqueous solution. Methods Enzmol. 1997, 289: 266.
    • (1997) Methods Enzmol. , vol.289 , pp. 266
    • Muir, T.W.1    Dawson, P.E.2    Kent, S.B.H.3
  • 24
    • 0033615313 scopus 로고    scopus 로고
    • Chemical protein synthesis by solid phase ligation of unprotected peptide segments
    • Canne, L. E., Botti, P., Simon, R. J. et al., Chemical protein synthesis by solid phase ligation of unprotected peptide segments, J. Am. Chem. Soc., 1999, 121(38): 8720.
    • (1999) J. Am. Chem. Soc. , vol.121 , Issue.38 , pp. 8720
    • Canne, L.E.1    Botti, P.2    Simon, R.J.3
  • 25
    • 0034630964 scopus 로고    scopus 로고
    • Bidirectional tandem pseudoproline ligations of proline-rich helical peptides
    • Miao, Z., Tam, J. P., Bidirectional tandem pseudoproline ligations of proline-rich helical peptides, J. Am. Chem. Soc., 2000, 122(18): 4253.
    • (2000) J. Am. Chem. Soc. , vol.122 , Issue.18 , pp. 4253
    • Miao, Z.1    Tam, J.P.2
  • 26
    • 0034831088 scopus 로고    scopus 로고
    • Tandem ligation of unprotected peptides through thiaprolyl and cysteinyl bonds in water
    • Tam, J. P., Yu, Q., Yang, J. L., Tandem ligation of unprotected peptides through thiaprolyl and cysteinyl bonds in water, J. Am. Chem. Soc., 2001, 123(11): 2487.
    • (2001) J. Am. Chem. Soc. , vol.123 , Issue.11 , pp. 2487
    • Tam, J.P.1    Yu, Q.2    Yang, J.L.3
  • 27
    • 0034990891 scopus 로고    scopus 로고
    • Development and application of expressed protein ligation
    • Muir, T. W., Development and application of expressed protein ligation, Synlett, 2001(6): 733.
    • (2001) Synlett , Issue.6 , pp. 733
    • Muir, T.W.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.