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Quantitative Evaluation of Dystrophin Expression Using SDS-PAGE Western Blot Methods
Margaret J Beatka1, Mariah J Prom1, Margaret Haberman1
1Diverge Translational Science Laboratory, Milwaukee, WI, USA.
None:
SDS-PAGE Western blots allow for the identification of the presence and relative quantity of proteins of interest on the basis of their molecular weight and their recognition by specific antibodies. This technique has historically been useful in the diagnosis and study of Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD), as it allows the recognition of clinically relevant abnormalities in the amount or size of dystrophin. While this technique is used infrequently for diagnosis at this point (as genetic testing for pathogenic variants of the DMD gene has become standard practice), it remains an important tool in basic science research and in the evaluation of therapies that restore or replace dystrophin expression. This chapter provides a technique that is suitable for the quantitative assessment of dystrophin expression in isolates of skeletal muscle tissue, based on our experience and guidance provided by the US Food and Drug Administration (FDA) for these types of assays. Topics associated with the design of quantitative Western blot techniques, options for loading control use, and the challenges associated with variable pathology within specimens are also discussed. Performing this technique can provide reproducible and reliable quantification of full-length or shortened dystrophin protein content in frozen muscle tissue.
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Western Blotting
The technique begins with separating proteins from the sample using sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), followed by protein transfer, immunoblotting, and finally, protein detection.
SDS-PAGE
A variation of gel electrophoresis, termed polyacrylamide gel electrophoresis (PAGE), is commonly used for separating proteins according to their molecular size by passing them through a polyacrylamide gel. Because of the varying charges associated with amino acid side chains, PAGE can be used to separate intact...