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Volumn 1126, Issue , 2008, Pages 248-252

Model studies on protein glycation: Influence of cysteine on the reactivity of arginine and lysine residues toward glyoxal

Author keywords

Carboxymethyllysine; Glyoxal; High hydrostatic pressure; Nucleophilic amino acids

Indexed keywords

ARGININE; BETA CASEIN; CYSTEINE; GLYOXAL; LYSINE;

EID: 42549164542     PISSN: 00778923     EISSN: 17496632     Source Type: Book Series    
DOI: 10.1196/annals.1433.021     Document Type: Conference Paper
Times cited : (13)

References (9)
  • 1
    • 0028934990 scopus 로고
    • Mechanism of protein modification by glyoxal and glycolaldehyde, reactive intermediates of the Maillard reaction
    • 1 Glomb, M.A. & V.M. Monnier. 1995. Mechanism of protein modification by glyoxal and glycolaldehyde, reactive intermediates of the Maillard reaction. J. Biol. Chem. 270: 10017–10026.
    • (1995) J. Biol. Chem. , vol.270 , pp. 10017-10026
    • Glomb, M.A.1    Monnier, V.M.2
  • 2
    • 0034826534 scopus 로고    scopus 로고
    • Isolation and characterization of glyoxal‐arginine modifications
    • 2 Glomb, M.A. & G. Lang. 2001. Isolation and characterization of glyoxal‐arginine modifications. J. Agric. Food Chem. 49: 1493–1501.
    • (2001) J. Agric. Food Chem. , vol.49 , pp. 1493-1501
    • Glomb, M.A.1    Lang, G.2
  • 3
    • 85120587347 scopus 로고    scopus 로고
    • Chemical modification of protein thiols in diabetes
    • 3 Baynes, J.W., N. Frizzell, R. Nagai, et al. 2006. Chemical modification of protein thiols in diabetes. Abstracts of Papers, 232nd ACS National Meeting, San Francisco, CA, United States, Sept. 10–14.
    • (2006)
    • Baynes, J.W.1    Frizzell, N.2    Nagai, R.3
  • 4
    • 0011328098 scopus 로고
    • Pathways of the Maillard Reaction in vitro and in vivo, in: Maillard Reactions in Chemistry, Food and Health
    • 4 Zyzak, D.V., K.J. Wells‐Knecht, J.A. Blackledge, et al. 1994. Pathways of the Maillard Reaction in vitro and in vivo. In Maillard Reactions in Chemistry, Food and Health. T.P. Labuza, G.A. Reineccius, et al., Eds.: 274–280. Royal Chemical Society. Bodmin, UK.
    • (1994) , pp. 274-280
    • Zyzak, D.V.1    Wells‐Knecht, K.J.2    Blackledge, J.A.3
  • 6
    • 23744447530 scopus 로고    scopus 로고
    • Dicarbonyl intermediates in the Maillard reaction
    • 6 Thornalley, P.J. 2005. Dicarbonyl intermediates in the Maillard reaction. Ann. N.Y. Acad. Sci. 1043: 111–117.
    • (2005) Ann. N.Y. Acad. Sci. , vol.1043 , pp. 111-117
    • Thornalley, P.J.1
  • 7
    • 33845780096 scopus 로고    scopus 로고
    • Protein and low molecular mass thiols as targets and inhibitors of glycation reactions
    • 7 Zeng, J. & M.J. Davies. 2006. Protein and low molecular mass thiols as targets and inhibitors of glycation reactions. Chem. Res. Toxicol. 19: 1668–1676.
    • (2006) Chem. Res. Toxicol. , vol.19 , pp. 1668-1676
    • Zeng, J.1    Davies, M.J.2
  • 8
    • 0000533829 scopus 로고
    • Efficient determination of individual Maillard compounds
    • 8 Henle, T., H. Walter, I. Krause & H. Klostermeyer. 1991. Efficient determination of individual Maillard compounds. Int. Dairy J. 1: 125–135.
    • (1991) Int. Dairy J. , vol.1 , pp. 125-135
    • Henle, T.1    Walter, H.2    Krause, I.3    Klostermeyer, H.4
  • 9
    • 23844502010 scopus 로고    scopus 로고
    • Evidence for the formation of adducts and S‐(Carboxymethyl)cysteine on reaction of a‐dicarbonyl compounds with thiol groups on amino acids, peptides, and proteins
    • 9 Zeng, J. & M.J. Davies. 2005. Evidence for the formation of adducts and S‐(Carboxymethyl)cysteine on reaction of a‐dicarbonyl compounds with thiol groups on amino acids, peptides, and proteins. Chem. Res. Toxicol. 18: 1232–1241.
    • (2005) Chem. Res. Toxicol. , vol.18 , pp. 1232-1241
    • Zeng, J.1    Davies, M.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.