d'Avignon A - Search Results

1

Human neutrophils employ the myeloperoxidase-hydrogen peroxide-chloride system to oxidize alpha-amino acids to a family of reactive aldehydes. Mechanistic studies identifying labile intermediates along the reaction pathway.

Hazen SL, d'Avignon A, Anderson MM, Hsu FF, Heinecke JW. Hazen SL, et al. J Biol Chem. 1998 Feb 27;273(9):4997-5005. doi: 10.1074/jbc.273.9.4997. J Biol Chem. 1998. PMID: 9478947 Free article.

2

Oxidative cross-linking of tryptophan to glycine restrains matrix metalloproteinase activity: specific structural motifs control protein oxidation.

Fu X, Kao JL, Bergt C, Kassim SY, Huq NP, d'Avignon A, Parks WC, Mecham RP, Heinecke JW. Fu X, et al. J Biol Chem. 2004 Feb 20;279(8):6209-12. doi: 10.1074/jbc.C300506200. Epub 2003 Dec 11. J Biol Chem. 2004. PMID: 14670964 Free article.

3

p-Hydroxyphenylacetaldehyde, the major product of L-tyrosine oxidation by the myeloperoxidase-H2O2-chloride system of phagocytes, covalently modifies epsilon-amino groups of protein lysine residues.

Hazen SL, Gaut JP, Hsu FF, Crowley JR, d'Avignon A, Heinecke JW. Hazen SL, et al. J Biol Chem. 1997 Jul 4;272(27):16990-8. doi: 10.1074/jbc.272.27.16990. J Biol Chem. 1997. PMID: 9202012 Free article.

4

Human neutrophils employ myeloperoxidase to convert alpha-amino acids to a battery of reactive aldehydes: a pathway for aldehyde generation at sites of inflammation.

Hazen SL, Hsu FF, d'Avignon A, Heinecke JW. Hazen SL, et al. Biochemistry. 1998 May 12;37(19):6864-73. doi: 10.1021/bi972449j. Biochemistry. 1998. PMID: 9578573

5

Synthesis, isolation, and characterization of the adduct formed in the reaction of p-hydroxyphenylacetaldehyde with the amino headgroup of phosphatidylethanolamine and phosphatidylserine.

Hazen SL, Heller J, Hsu FF, d'Avignon A, Heinecke JW. Hazen SL, et al. Chem Res Toxicol. 1999 Jan;12(1):19-27. doi: 10.1021/tx980147s. Chem Res Toxicol. 1999. PMID: 9894014

6

Specific sequence motifs direct the oxygenation and chlorination of tryptophan by myeloperoxidase.

Fu X, Wang Y, Kao J, Irwin A, d'Avignon A, Mecham RP, Parks WC, Heinecke JW. Fu X, et al. Biochemistry. 2006 Mar 28;45(12):3961-71. doi: 10.1021/bi052339+. Biochemistry. 2006. PMID: 16548523 Free PMC article.

7

3-Bromotyrosine and 3,5-dibromotyrosine are major products of protein oxidation by eosinophil peroxidase: potential markers for eosinophil-dependent tissue injury in vivo.

Wu W, Chen Y, d'Avignon A, Hazen SL. Wu W, et al. Biochemistry. 1999 Mar 23;38(12):3538-48. doi: 10.1021/bi982401l. Biochemistry. 1999. PMID: 10090740

8

19F nuclear magnetic resonance studies of 6-fluorotryptophan-substituted rat cellular retinol binding protein II produced in Escherichia coli. An analysis of four tryptophan substitution mutants and their interactions with all-trans-retinol.

Li E, Qian SJ, Yang NC, d'Avignon A, Gordon JI. Li E, et al. J Biol Chem. 1990 Jul 15;265(20):11549-54. J Biol Chem. 1990. PMID: 2195021 Free article.

9

Nuclear magnetic resonance studies of 6-fluorotryptophan-substituted rat cellular retinol-binding protein II produced in Escherichia coli. Analysis of the apoprotein and the holoprotein containing bound all-trans-retinol and all-trans-retinal.

Li E, Quian SJ, Nader L, Yang NC, d'Avignon A, Sacchettini JC, Gordon JI. Li E, et al. J Biol Chem. 1989 Oct 15;264(29):17041-8. J Biol Chem. 1989. PMID: 2676998 Free article.

10

Differential binding of retinol analogs to two homologous cellular retinol-binding proteins.

Rong D, Lovey AJ, Rosenberger M, d'Avignon A, Ponder J, Li E. Rong D, et al. J Biol Chem. 1993 Apr 15;268(11):7929-34. J Biol Chem. 1993. PMID: 8463314 Free article.

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