Document Detail


Characterization of the 4 S polycyclic aromatic hydrocarbon-binding protein in human liver and cells.
MedLine Citation:
PMID:  1416973     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The 4 S polycyclic aromatic hydrocarbon (PAH)-binding protein (PBP) is a soluble protein that binds PAHs with high affinity in mouse, rat, and rabbit. Until now, this protein had not been detected in human placenta or human cells in culture by cytosol labeling and gradient centrifugation assay. Thanks to a preliminary fractionation of cytosol by sedimentation on sucrose gradient or/and gel permeation chromatography, we found that PBP was present in liver, MCF-7 cell line, and hepatocytes of human. To accurately quantitate PBP binding and determine specific binding parameters, a reduction in the amount of charcoal used to adsorb nonspecifically bound benzo[a]pyrene was required. By saturation analysis, the concentration of specific binding sites for [3H]BP in PBP fraction from human liver was 4.6 pmol/mg of protein compared with 14.7 +/- 1.4 pmol/mg in the same fraction from DBA/2J mouse liver. Kinetic studies analyzed by Scatchard and Woolf plots indicate that human liver and MCF-7 cells contain a low-affinity PBP form: the Kd derived from Woolf plot analysis were 14.2 +/- 1.4 and 26.2 +/- 1.8 nM, respectively. DBA/2J mouse possesses a higher-affinity PBP form, the same analysis indicating a Kd of 6.1 +/- 0.3 nM. These data demonstrate that, by comparison to the mouse liver, a lower-affinity form of PBP is present in reduced concentration in human liver, explaining the impossibility of detecting this protein by sedimentation of human cytosol in sucrose gradient.
Authors:
B Peryt; P Maurel; P Lesca
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Archives of biochemistry and biophysics     Volume:  298     ISSN:  0003-9861     ISO Abbreviation:  Arch. Biochem. Biophys.     Publication Date:  1992 Nov 
Date Detail:
Created Date:  1992-11-13     Completed Date:  1992-11-13     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0372430     Medline TA:  Arch Biochem Biophys     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  420-30     Citation Subset:  IM    
Affiliation:
Department of Biochemistry, Institute of Biopharmacy, Warsaw, Poland.
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MeSH Terms
Descriptor/Qualifier:
Animals
Benzo(a)pyrene / metabolism*
Binding Sites
Breast Neoplasms
Carrier Proteins / isolation & purification,  metabolism*
Cell Fractionation
Cells, Cultured
Centrifugation, Density Gradient
Cytosol / metabolism
Female
Glycine N-Methyltransferase
Humans
Liver / drug effects,  metabolism*
Male
Methyltransferases*
Mice
Mice, Inbred C57BL
Mice, Inbred DBA
Pyridines / pharmacology
Tetrachlorodibenzodioxin / metabolism*
Tumor Cells, Cultured
Chemical
Reg. No./Substance:
0/Carrier Proteins; 0/Pyridines; 1746-01-6/Tetrachlorodibenzodioxin; 50-32-8/Benzo(a)pyrene; 76150-91-9/1,4-bis(2-(3,5-dichloropyridyloxy))benzene; EC 2.1.1.-/Methyltransferases; EC 2.1.1.20/Glycine N-Methyltransferase

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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