Quantitative Estimation of Dystrophin Protein: A Sensitive and Convenient "Two-Antibody Sandwich" ELISA.
- 1 January 1996
- journal article
- Published by Tohoku University Medical Press in The Tohoku Journal of Experimental Medicine
- Vol. 180 (1), 57-63
- https://doi.org/10.1620/tjem.180.57
Abstract
As dystrophin protein, the protein product of Duchenne muscular dystrophy (DMD) gene, represents only 0.002 approximately 0.03% of the total muscle proteins and human dystrophin protein has not been purified, quantitative estimation of this protein has been difficult. We describe a sensitive, reliable and convenient "two-antibody sandwich" enzyme-linked immunosorbent assay (ELISA) using commercially available monoclonal antibodies. This system, using a capture antibody specific for carboxyl terminus and two different detection antibodies for the mid-rod domain and the amino-terminal domain, is highly specific for dystrophin, since muscle specimens from DMD patients gave almost zero response (n = 3, 0.38 approximately 0.45%; expressed as a percentage of normal muscle tissue). This assay should prove to be an accessible and useful tool for the diagnosis of DMD/BMD and for the evaluation in clinical trials such as myoblast transfer and gene therapy.Keywords
This publication has 14 references indexed in Scilit:
- Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophyHuman Molecular Genetics, 1995
- Expression of full-length and truncated dystrophin mini-genes in transgenic mdx miceHuman Molecular Genetics, 1995
- A quantitative ELISA for dystrophinJournal of Immunological Methods, 1993
- Is the maintainance of the C-terminus domain of dystrophin enough to ensure a milder Becker muscular dystrophy phenotype?Human Molecular Genetics, 1993
- Normal dystrophin transcripts detected in Duchenne muscular dystrophy patients after myoblast transplantationNature, 1992
- ELISA quantitation of dystrophin for the diagnosis of Duchenne and Becker muscular dystrophiesNeurology, 1992
- Preservation of the C-terminus of dystrophin molecule in the skeletal muscle from Becker muscular dystrophyJournal of the Neurological Sciences, 1991
- Improved diagnosis of Becker muscular dystrophy by dystrophin testingNeurology, 1989
- Characterization of Dystrophin in Muscle-Biopsy Specimens from Patients with Duchenne's or Becker's Muscular DystrophyNew England Journal of Medicine, 1988
- Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individualsCell, 1987