Differential signatures of protein glycosylation and phosphorylation in human Chang liver cells induced by TCDD treatment

Kim, JH; In, YJ; Kim, WK; Bae, KH; Kang, S; Lee, SC

HERO ID

199075

Reference Type

Journal Article

Year

2008

Language

English

PMID

18358643

HERO ID 199075
In Press No
Year 2008
Title Differential signatures of protein glycosylation and phosphorylation in human Chang liver cells induced by TCDD treatment
Authors Kim, JH; In, YJ; Kim, WK; Bae, KH; Kang, S; Lee, SC
Journal Toxicology Letters
Volume 178
Issue 1
Page Numbers 20-28
Abstract Dioxins are a class of polyhalogenated aromatic hydrocarbons that induces a wide spectrum of toxic responses in animals. Health effects have been studied intensively, but the detailed molecular mechanisms are quite complex and not yet fully understood. In this study, the effects of model dioxin, 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) on protein modifications such as glycosylation and phosphorylation were extensively studied. Using 2-D electrophoresis, various protein visualizations techniques, protein modification-dependent enrichments techniques and mass spectrometry, we performed comparative proteomic investigations on Chang human liver cells before and after the treatment with TCDD. Many glycoproteins and phosphoproteins were found to be affected by the TCDD treatment. The glycosylations on Cathepsin B, HSP60, the subunit 5 of chaperonin containing TCP1 complex, and Prolyl 4-hydroxylase beta-subunit were increased. Heat shock 70 kDa protein 5 and ATP synthase beta subunit showed enhanced or reduced phosphorylation, respectively. Two microtubule associated proteins, Microtubule-associated protein 1S and ARP1 actin-related protein 1 homolog A showed enhanced tyrosine phosphorylation. The data in this study provide interesting insights on the molecular and biochemical events of TCDD-mediated toxicities.
Doi 10.1016/j.toxlet.2008.01.019
Pmid 18358643
Wosid WOS:000255828900003
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English
Keyword Dioxin; Liver; Proteomics; Phosphorylation; Glycosylation
Is Qa No