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Volumn 335, Issue 1, 2004, Pages 168-170

General method for facile intramolecular disulfide formation in synthetic peptides

Author keywords

[No Author keywords available]

Indexed keywords

BIOCHEMISTRY; CHEMISTRY;

EID: 7444250679     PISSN: 00032697     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ab.2004.07.015     Document Type: Article
Times cited : (16)

References (9)
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    • Discovery of a highly selective and efficient reagent for formation of intramolecular disulfide bonds in peptides
    • T. Shi, and D.L. Rabenstein Discovery of a highly selective and efficient reagent for formation of intramolecular disulfide bonds in peptides J. Am. Chem. Soc. 122 2000 6809 6815
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 6809-6815
    • Shi, T.1    Rabenstein, D.L.2
  • 3
    • 0033603382 scopus 로고    scopus 로고
    • Trans-Dichlorotetracyanoplatinate(IV) as a reagent for the rapid and quantitative formation of intramolecular disulfide bonds in peptides
    • T. Shi, and D.L. Rabenstein trans-Dichlorotetracyanoplatinate(IV) as a reagent for the rapid and quantitative formation of intramolecular disulfide bonds in peptides J. Org. Chem. 64 1999 4590 4595
    • (1999) J. Org. Chem. , vol.64 , pp. 4590-4595
    • Shi, T.1    Rabenstein, D.L.2
  • 5
    • 0032813187 scopus 로고    scopus 로고
    • 2,2′-Bispyridyl disulfide rapidly induces intramolecular disulfide bonds in peptides
    • K. Maruyama, H. Nagasawa, and A. Suzuki 2,2′-Bispyridyl disulfide rapidly induces intramolecular disulfide bonds in peptides Peptides 20 1999 881 884
    • (1999) Peptides , vol.20 , pp. 881-884
    • Maruyama, K.1    Nagasawa, H.2    Suzuki, A.3
  • 6
    • 0018861668 scopus 로고
    • A kinetic method for the study of solvent environments of thiol groups in proteins involving the use of a pair of isomeric reactivity probes and a differential solvent effect. Investigation of the active centre of ficin by using 2,2′- and 4,4′-dipyridyl disulphides as reactivity probes
    • J.P. Malthouse, and K. Brocklehurst A kinetic method for the study of solvent environments of thiol groups in proteins involving the use of a pair of isomeric reactivity probes and a differential solvent effect. Investigation of the active centre of ficin by using 2,2′- and 4,4′-dipyridyl disulphides as reactivity probes Biochem. J. 185 1980 217 222
    • (1980) Biochem. J. , vol.185 , pp. 217-222
    • Malthouse, J.P.1    Brocklehurst, K.2
  • 7
    • 0037433511 scopus 로고    scopus 로고
    • Effects of As(III) binding on α-helical structure
    • D.J. Cline, C. Thorpe, and J.P. Schneider Effects of As(III) binding on α-helical structure J. Am. Chem. Soc. 125 2003 2923 2929
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 2923-2929
    • Cline, D.J.1    Thorpe, C.2    Schneider, J.P.3
  • 8
    • 0347989354 scopus 로고    scopus 로고
    • Structure-based design of a fluorimetric redox active peptide probe
    • D.J. Cline, C. Thorpe, and J.P. Schneider Structure-based design of a fluorimetric redox active peptide probe Anal. Biochem. 325 2004 144 150
    • (2004) Anal. Biochem. , vol.325 , pp. 144-150
    • Cline, D.J.1    Thorpe, C.2    Schneider, J.P.3
  • 9
    • 0018416496 scopus 로고
    • Ellman's reagent - 5,5′-dithiobis(2-nitrobenzoic acid) - Re-examination
    • P.W. Riddles, R.L. Blakeley, and B. Zerner Ellman's reagent - 5,5′-dithiobis(2-nitrobenzoic acid) - re-examination Anal. Biochem. 94 1979 75 81
    • (1979) Anal. Biochem. , vol.94 , pp. 75-81
    • Riddles, P.W.1    Blakeley, R.L.2    Zerner, B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.