Production of rabbit polyclonal antibody against apobec-1 by genetic immunization

Circulating apolipoprotein B (apoB) exists in two forms; apoB-100 and apoB-48. ApoB-48 is a truncated form of apoB resulting from RNA editing. The editing enzyme, called apobec-1, converts a cytidine (C) at nucleotide 6666 in apoB 100 mRNA to a uridine (U) and changes a CAA codon to an in-frame stop...

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Main Authors: S C Yeung, J Anderson, K Kobayashi, K Oka, L Chan
Format: Article
Language:English
Published: Elsevier 1997-12-01
Series:Journal of Lipid Research
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520300468
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spelling doaj-b4f153d41ebb4c3082ed817b9f40ce872021-04-26T05:45:32ZengElsevierJournal of Lipid Research0022-22751997-12-01381226272632Production of rabbit polyclonal antibody against apobec-1 by genetic immunizationS C Yeung0J Anderson1K Kobayashi2K Oka3L Chan4Department of Cell Biology, Baylor College of Medicine, Houston, TX 77030, USA.Department of Cell Biology, Baylor College of Medicine, Houston, TX 77030, USA.Department of Cell Biology, Baylor College of Medicine, Houston, TX 77030, USA.Department of Cell Biology, Baylor College of Medicine, Houston, TX 77030, USA.Department of Cell Biology, Baylor College of Medicine, Houston, TX 77030, USA.Circulating apolipoprotein B (apoB) exists in two forms; apoB-100 and apoB-48. ApoB-48 is a truncated form of apoB resulting from RNA editing. The editing enzyme, called apobec-1, converts a cytidine (C) at nucleotide 6666 in apoB 100 mRNA to a uridine (U) and changes a CAA codon to an in-frame stop codon, UAA. We have produced a specific rabbit polyclonal antiserum against apobec-1 by genetic immunization. The cDNA of mouse apobec-1 was inserted downstream and in-frame at the BamH I site in the last exon of human growth hormone cDNA driven by a cytomegalovirus promoter. This plasmid was injected together with another plasmid expressing granulocyte macrophage colony-stimulating factor into the thigh muscles of a rabbit. The resulting antiserum demonstrated high specificity on Western blots, and inhibited the apoB mRNA editing activity of mouse liver extract in a dose-dependent manner. This report demonstrates that DNA immunization is a powerful technique that can be readily applied to other sparse or difficult-to-purify proteins in lipid metabolism.http://www.sciencedirect.com/science/article/pii/S0022227520300468
collection DOAJ
language English
format Article
sources DOAJ
author S C Yeung
J Anderson
K Kobayashi
K Oka
L Chan
spellingShingle S C Yeung
J Anderson
K Kobayashi
K Oka
L Chan
Production of rabbit polyclonal antibody against apobec-1 by genetic immunization
Journal of Lipid Research
author_facet S C Yeung
J Anderson
K Kobayashi
K Oka
L Chan
author_sort S C Yeung
title Production of rabbit polyclonal antibody against apobec-1 by genetic immunization
title_short Production of rabbit polyclonal antibody against apobec-1 by genetic immunization
title_full Production of rabbit polyclonal antibody against apobec-1 by genetic immunization
title_fullStr Production of rabbit polyclonal antibody against apobec-1 by genetic immunization
title_full_unstemmed Production of rabbit polyclonal antibody against apobec-1 by genetic immunization
title_sort production of rabbit polyclonal antibody against apobec-1 by genetic immunization
publisher Elsevier
series Journal of Lipid Research
issn 0022-2275
publishDate 1997-12-01
description Circulating apolipoprotein B (apoB) exists in two forms; apoB-100 and apoB-48. ApoB-48 is a truncated form of apoB resulting from RNA editing. The editing enzyme, called apobec-1, converts a cytidine (C) at nucleotide 6666 in apoB 100 mRNA to a uridine (U) and changes a CAA codon to an in-frame stop codon, UAA. We have produced a specific rabbit polyclonal antiserum against apobec-1 by genetic immunization. The cDNA of mouse apobec-1 was inserted downstream and in-frame at the BamH I site in the last exon of human growth hormone cDNA driven by a cytomegalovirus promoter. This plasmid was injected together with another plasmid expressing granulocyte macrophage colony-stimulating factor into the thigh muscles of a rabbit. The resulting antiserum demonstrated high specificity on Western blots, and inhibited the apoB mRNA editing activity of mouse liver extract in a dose-dependent manner. This report demonstrates that DNA immunization is a powerful technique that can be readily applied to other sparse or difficult-to-purify proteins in lipid metabolism.
url http://www.sciencedirect.com/science/article/pii/S0022227520300468
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