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Xylosyltransferase II is the predominant isoenzyme which is responsible for the steady-state level of xylosyltransferase activity in human serum.
Kuhn, Joachim; Götting, Christian; Beahm, Brendan J; Bertozzi, Carolyn R; Faust, Isabel; Kuzaj, Patricia; Knabbe, Cornelius; Hendig, Doris.
Afiliação
  • Kuhn J; Institut für Laboratoriums- und Transfusionsmedizin, Herz- und Diabeteszentrum Nordrhein-Westfalen, Universitätsklinik der Ruhr-Universität Bochum, Georgstraße 11, 32545 Bad Oeynhausen, Germany. Electronic address: jkuhn@hdz-nrw.de.
  • Götting C; MVZ Labor Limbach Nürnberg, Lina-Ammon-Strasse 28, 90471 Nürnberg, Germany.
  • Beahm BJ; Department of Chemistry and Molecular and Cell Biology Howard Hughes Medical Institute University of California, Berkeley, CA 94720, USA.
  • Bertozzi CR; Department of Chemistry and Molecular and Cell Biology Howard Hughes Medical Institute University of California, Berkeley, CA 94720, USA.
  • Faust I; Institut für Laboratoriums- und Transfusionsmedizin, Herz- und Diabeteszentrum Nordrhein-Westfalen, Universitätsklinik der Ruhr-Universität Bochum, Georgstraße 11, 32545 Bad Oeynhausen, Germany.
  • Kuzaj P; Institut für Laboratoriums- und Transfusionsmedizin, Herz- und Diabeteszentrum Nordrhein-Westfalen, Universitätsklinik der Ruhr-Universität Bochum, Georgstraße 11, 32545 Bad Oeynhausen, Germany.
  • Knabbe C; Institut für Laboratoriums- und Transfusionsmedizin, Herz- und Diabeteszentrum Nordrhein-Westfalen, Universitätsklinik der Ruhr-Universität Bochum, Georgstraße 11, 32545 Bad Oeynhausen, Germany.
  • Hendig D; Institut für Laboratoriums- und Transfusionsmedizin, Herz- und Diabeteszentrum Nordrhein-Westfalen, Universitätsklinik der Ruhr-Universität Bochum, Georgstraße 11, 32545 Bad Oeynhausen, Germany.
Biochem Biophys Res Commun ; 459(3): 469-74, 2015 Apr 10.
Article em En | MEDLINE | ID: mdl-25748573
ABSTRACT
In mammals, two active xylosyltransferase isoenzymes (EC 2.4.2.16) exist. Both xylosyltransferases I and II (XT-I and XT-II) catalyze the transfer of xylose from UDP-xylose to select serine residues in the proteoglycan core protein. Altered XT activity in human serum was found to correlate directly with various diseases such as osteoarthritis, systemic sclerosis, liver fibrosis, and pseudoxanthoma elasticum. To interpret the significance of the enzyme activity alteration observed in disease states it is important to know which isoenzyme is responsible for the XT activity in serum. Until now it was impossible for a specific measurement of XT-I or XT-II activity, respectively, because of the absence of a suitable enzyme substrate. This issue has now been solved and the following experimental study demonstrates for the first time, via the enzyme activity that XT-II is the predominant isoenzyme responsible for XT activity in human serum. The proof was performed using natural UDP-xylose as the xylose donor, as well as the artificial compound UDP-4-azido-4-deoxyxylose, which is a selective xylose donor for XT-I.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Pentosiltransferases Limite: Humans Idioma: En Revista: Biochem Biophys Res Commun Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Pentosiltransferases Limite: Humans Idioma: En Revista: Biochem Biophys Res Commun Ano de publicação: 2015 Tipo de documento: Article