Production and application of polyclonal antibody against mouse frataxin.
- Author:
Shuangying HAO
1
;
Fangxia XU
1
;
Kuanyu LI
1
Author Information
1. Jiangsu Key Laboratory for Molecular Medicine, Medical School of Nanjing University, Nanjing 210093, Jiangsu, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Antibodies;
immunology;
metabolism;
Antibody Specificity;
immunology;
Escherichia coli;
genetics;
metabolism;
Female;
Genetic Engineering;
methods;
Immunization;
Iron-Binding Proteins;
genetics;
immunology;
Mice;
Rabbits;
Recombinant Fusion Proteins;
biosynthesis;
genetics;
immunology
- From:
Chinese Journal of Biotechnology
2013;29(9):1313-1322
- CountryChina
- Language:Chinese
-
Abstract:
Friedreich ataxia (FRDA) is an autosomal recessive neurodegenerative disease caused by reduced expression levels of the frataxin gene (FXN) due to expansion of triplet nucleotide GAA repeats in the first intron of FXN. FXN is a mitochondrial protein which plays an important role in the regulation of intracellular iron trafficking, biogenesis of iron-sulfur cluster and heme, and removal of reactive oxygen species. Our previous work showed that tissue-specific expression of FXN in cerebellum and heart generates two novel isoforms. In order to find the isoforms in mouse tissues, we tried to obtain a polyclonal antibody against mouse Fxn with high specificity and sensitivity. Thus, the recombinant plasmid pET24(+)-mFxn was constructed to express his-tagged Fxn in BL21 (DE3) cells. The expressed protein is a mature form with 130 amino acids (aa, 14.38 kDa) without the N-terminal signal peptide (77 aa), purified on Ni-NTA column and further dialyzed with Centrifugal Filtration Device. The polyclonal antibody against Fxn was produced by immunizing rabbits with highly purified protein. The collected antiserums were preliminarily purified by precipitation with (NH4)2SO4. Western blotting analysis and cell immunofluorescence showed that the obtained antibody was able to detect both purified and endogenous Fxn. It also worked well in immunoprecipitation with mouse tissues. This is the first time, to our knowledge, to report that mouse Fxn was used as immunogen to generate antibody with high specificity and sensitivity. This work provides a powerful tool for our further research on mouse Fxn isoforms.
