Absence of Vitamin K-Dependent gamma-Carboxylation in Human Periostin Extracted from Fibrotic Lung or Secreted from a Cell Line Engineered to Optimize gamma-Carboxylation

作者：Annis Douglas S; Ma Hanqing; Balas Danika M; Kumfer Kraig T; Sandbo Nathan; Potts Gregory K; Coon Joshua J; Mosher Deane F^*

来源：PLos One, 2015, 10(8): e0135374.

DOI：10.1371/journal.pone.0135374

Periostin (PN, gene name POSTN) is an extracellular matrix protein that is up-regulated in bronchial epithelial cells and lung fibroblasts by TH-2 cytokines. Its paralog, TGF-beta-induced protein (beta ig-h3, gene name TGFBI), is also expressed in the lung and up-regulated in bronchial myofibroblasts by TGF-beta. PN and beta ig-h3 contain fasciclin 1 modules that harbor putative recognition sequences for gamma-glutamyl carboxylase and are annotated in UniProt as undergoing vitamin K-dependent gamma-carboxylation of multiple glutamic acid residues. gamma-carboxylation profoundly alters activities of other proteins subject to the modification, e.g., blood coagulation factors, and would be expected to alter the structure and function of PN and beta ig-h3. To analyze for the presence of gamma-carboxylation, proteins extracted from fibrotic lung were reacted with monoclonal antibodies specific for PN, beta ig-h3, or modification with gamma-carboxyglutamic acid (Gla). In Western blots of 1-dimensional gels, bands stained with anti-PN or -beta ig-h3 did not match those stained with anti-Gla. In 2-dimensional gels, anti-PN-positive spots had pIs of 7.0 to > 8, as expected for the unmodified protein, and there was no overlap between anti-PN-positive and anti-Gla-positive spots. Recombinant PN and blood coagulation factor VII were produced in HEK293 cells that had been transfected with vitamin K 2, 3-epoxide reductase C1 to optimize gamma-carboxylation. Recombinant PN secreted from these cells did not react with anti-Gla antibody and had pIs similar to that found in extracts of fibrotic lung whereas secreted factor VII reacted strongly with anti-Gla antibody. Over 67% coverage of recombinant PN was achieved by mass spectrometry, including peptides with 19 of the 24 glutamates considered targets of gamma-carboxylation, but analysis revealed no modification. Over 86% sequence coverage and three modified glutamic acid residues were identified in recombinant fVII. These data indicate that PN and beta ig-h3 are not subject to vitamin K-dependent gamma-carboxylation.

• 出版日期2015-8-14