메뉴 건너뛰기




Volumn 12, Issue 11, 2006, Pages 734-738

Determination of glyoxylyl-peptide concentration using oxime chemistry and RP-HPLC analysis

Author keywords

Glyoxylyl peptide; O benzylhydroxylamine; Oxime

Indexed keywords

OXIME; PEPTIDE DERIVATIVE;

EID: 33750743387     PISSN: 10752617     EISSN: 10991387     Source Type: Journal    
DOI: 10.1002/psc.791     Document Type: Article
Times cited : (7)

References (21)
  • 1
    • 0001671290 scopus 로고
    • Conversion of the N-terminal serine residue of corticotrophin into glycine
    • Dixon HBF, Weitkamp LR. Conversion of the N-terminal serine residue of corticotrophin into glycine. Biochem. J. 1962; 84: 462-468.
    • (1962) Biochem. J. , vol.84 , pp. 462-468
    • Dixon, H.B.F.1    Weitkamp, L.R.2
  • 2
    • 0026826660 scopus 로고
    • Site-directed conjugation of nonpeptide groups to peptides and proteins via periodate oxidation of a 2-amino alcohol. Application to modification at N-terminal serine
    • Geoghegan KF, Stroh JG. Site-directed conjugation of nonpeptide groups to peptides and proteins via periodate oxidation of a 2-amino alcohol. Application to modification at N-terminal serine. Bioconjugate Chem. 1992; 3: 138-146.
    • (1992) Bioconjugate Chem. , vol.3 , pp. 138-146
    • Geoghegan, K.F.1    Stroh, J.G.2
  • 3
    • 0028960723 scopus 로고
    • Unprotected peptides as building blocks for the synthesis of peptide dendrimers with oxime, hydrazone, and thiazolidine linkages
    • Shao J, Tam JP. Unprotected peptides as building blocks for the synthesis of peptide dendrimers with oxime, hydrazone, and thiazolidine linkages. J. Am. Chem. Soc. 1995; 117: 3893-3899.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 3893-3899
    • Shao, J.1    Tam, J.P.2
  • 4
    • 0033588281 scopus 로고    scopus 로고
    • A new linker for the synthesis of peptide α-oxo aldehydes
    • Fruchart JS, Gras-Masse H, Melnyk O. A new linker for the synthesis of peptide α-oxo aldehydes. Tetrahedron Lett. 1999; 40: 6225-6228.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 6225-6228
    • Fruchart, J.S.1    Gras-Masse, H.2    Melnyk, O.3
  • 5
    • 0035874754 scopus 로고    scopus 로고
    • A tartric acid-based linker for the solid phase synthesis of C-terminal peptide α-oxo aldehydes
    • Melnyk O, Fruchart JS, Grandjean C, Gras-Masse H. A tartric acid-based linker for the solid phase synthesis of C-terminal peptide α-oxo aldehydes. J. Org. Chem. 2001; 66: 4153-4160.
    • (2001) J. Org. Chem. , vol.66 , pp. 4153-4160
    • Melnyk, O.1    Fruchart, J.S.2    Grandjean, C.3    Gras-Masse, H.4
  • 6
    • 0036330701 scopus 로고    scopus 로고
    • C-terminal glyoxylyl peptides for sensitive enzyme-linked immunosorbent assays
    • Urbès F, Fruchart JS, Gras-Masse H, Melnyk O. C-terminal glyoxylyl peptides for sensitive enzyme-linked immunosorbent assays. Lett. Pept. Set 2002; 8: 253-258.
    • (2002) Lett. Pept. Set , vol.8 , pp. 253-258
    • Urbès, F.1    Fruchart, J.S.2    Gras-Masse, H.3    Melnyk, O.4
  • 7
    • 0742304331 scopus 로고    scopus 로고
    • A novel α,α′-diaminoacetic acid derivative for the introduction of the α-oxo aldehyde functionality into peptides
    • Far S, Melnyk O. A novel α,α′-diaminoacetic acid derivative for the introduction of the α-oxo aldehyde functionality into peptides. Tetrahedron Lett. 2004; 45: 1271-1273.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 1271-1273
    • Far, S.1    Melnyk, O.2
  • 8
    • 4444332560 scopus 로고    scopus 로고
    • Synthesis of glyoxylyl peptides using a phosphine labile α,α′-diaminoacetic acid derivative
    • Far S, Melnyk O. Synthesis of glyoxylyl peptides using a phosphine labile α,α′-diaminoacetic acid derivative. Tetrahedron Lett. 2004; 45: 7163-7165.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 7163-7165
    • Far, S.1    Melnyk, O.2
  • 9
    • 21844433446 scopus 로고    scopus 로고
    • Synthesis of glyoxylyl peptides using an Fmoc-protected α,α′-diaminoacetic acid derivative
    • Far S, Melnyk O. Synthesis of glyoxylyl peptides using an Fmoc-protected α,α′-diaminoacetic acid derivative. J. Pept. Sci. 2004; 11: 424-430.
    • (2004) J. Pept. Sci. , vol.11 , pp. 424-430
    • Far, S.1    Melnyk, O.2
  • 10
    • 0029140496 scopus 로고
    • Total chemical synthesis of a unique transcription factor-related protein: cMyc-Mac
    • Canne LE, Ferré-D'Amaré AR, Burley SK, Kent SBH. Total chemical synthesis of a unique transcription factor-related protein: cMyc-Mac. J. Am. Chem. Soc. 1995; 117: 2998-3007.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 2998-3007
    • Canne, L.E.1    Ferré-D'Amaré, A.R.2    Burley, S.K.3    Kent, S.B.H.4
  • 11
    • 0028231302 scopus 로고
    • Facile synthesis of homogeneous artificial proteins
    • Rose K. Facile synthesis of homogeneous artificial proteins. J. Am. Chem. Soc. 1994; 116: 30-33.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 30-33
    • Rose, K.1
  • 12
    • 0037908896 scopus 로고    scopus 로고
    • A novel method for the rational construction of well-defined immunogens: The use of oximation to conjugate cholera toxin B subunit to a peptide-polyoxime complex
    • Chen J, Zeng W, Offord R, Rose S. A novel method for the rational construction of well-defined immunogens: the use of oximation to conjugate cholera toxin B subunit to a peptide-polyoxime complex. Bioconjugate Chem. 2003; 14: 614-618.
    • (2003) Bioconjugate Chem. , vol.14 , pp. 614-618
    • Chen, J.1    Zeng, W.2    Offord, R.3    Rose, S.4
  • 13
    • 0023055743 scopus 로고
    • Preparation of protein conjugates via intermolecular hydrazone linkage
    • King TP, Zhao SW, Lam T. Preparation of protein conjugates via intermolecular hydrazone linkage. Biochemistry 1986; 25: 5774-5779.
    • (1986) Biochemistry , vol.25 , pp. 5774-5779
    • King, T.P.1    Zhao, S.W.2    Lam, T.3
  • 14
    • 0028947942 scopus 로고
    • Unprotected peptides as building blocks for branched peptides and peptide dendrimers
    • Spetzler JC, Tam JP. Unprotected peptides as building blocks for branched peptides and peptide dendrimers. Int. J. Pept. Protein Res. 1995; 45: 78-85.
    • (1995) Int. J. Pept. Protein Res. , vol.45 , pp. 78-85
    • Spetzler, J.C.1    Tam, J.P.2
  • 17
    • 0015007720 scopus 로고
    • Micro method for determination of reactive carbonyl groups in proteins and peptides using 2,4-dinitrophenylhydrazine
    • Fields R, Dixon HBF. Micro method for determination of reactive carbonyl groups in proteins and peptides using 2,4-dinitrophenylhydrazine. Biochem. J. 1971; 121: 587-589.
    • (1971) Biochem. J. , vol.121 , pp. 587-589
    • Fields, R.1    Dixon, H.B.F.2
  • 19
    • 0025232814 scopus 로고
    • Solid phase peptide synthesis utilizing 9-fluorenylmethoxy carbonyl amino acids
    • Fields GB, Noble RL. Solid phase peptide synthesis utilizing 9-fluorenylmethoxy carbonyl amino acids. Int. J Pept. Protein Res. 1990; 35: 161-214.
    • (1990) Int. J Pept. Protein Res. , vol.35 , pp. 161-214
    • Fields, G.B.1    Noble, R.L.2
  • 21
    • 0004204553 scopus 로고
    • In (3rd edn), Masson M, Tyson J, Stockwell P (eds). Ellis Horwood and Prentice Hall: New York
    • Miller JC, Miller JN. In Statistics for Analytical Chemistry (3rd edn), Masson M, Tyson J, Stockwell P (eds). Ellis Horwood and Prentice Hall: New York, 1993.
    • (1993) Statistics for Analytical Chemistry
    • Miller, J.C.1    Miller, J.N.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.