4.7 Article

Pharmacoproteomics of 4-phenylbutyrate-treated IB3-1 cystic fibrosis bronchial epithelial cells

期刊

JOURNAL OF PROTEOME RESEARCH
卷 5, 期 3, 页码 562-571

出版社

AMER CHEMICAL SOC
DOI: 10.1021/pr050319o

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cystic fibrosis; chaperone; chloride transport; proteasome; two-dimensional gel electrophoresis

资金

  1. NHLBI NIH HHS [R01 HL 59410, N01 BAA HL 02-04] Funding Source: Medline

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4-Phenylbutyrate (4-PBA) is an oral butyrate derivative that has recently been approved for treatment of urea cycle disorders and is under investigation in clinical trials of cancer, hemoglobinopathies, and cystic fibrosis (CF). We hypothesized that proteome profiling of 1B3-1 cystic fibrosis bronchial epithelial cells treated with 4-PBA would identify butyrate-responsive cellular chaperones, protein processing enzymes, and cell trafficking molecules associated with the amelioration of the chloride transport defect in these cells. Protein profiles were analyzed by two-dimensional gel electrophoresis and mass spectrometry. Over a p/ range of 4-7 and molecular weight from 20 to 150 kDa a total of 85 differentially expressed proteins were detected. Most of the identified proteins were chaperones, catalytic enzymes, and proteins comprising structural elements, cellular defense, protein biosynthesis, trafficking activity, and ion transport. Subsets of these proteins were confirmed by immunoblot analysis. These data represent a first-draft of the pharmacoproteornics map of 4-PBA treated cystic fibrosis bronchial epithelial cells.

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