Challenges of Interpreting Dystrophin Content by Western Blot

The Duchenne muscular dystrophy community has recently seen the first approved therapy for the restoration of dystrophin, based on its ability to increase levels of dystrophin protein, as determined by western blot. The approval, along with the initiation of clinical trials evaluating other dystrophin-restoring therapies, highlights the importance of accurate dystrophin quantitation. Nonoptimized western blot methods can reflect inaccurate results, especially in the quantitation of low dystrophin levels. A few key changes to standards and data analysis parameters can result in a low level of dystrophin (<0.5% of a healthy biopsy) being inaccurately interpreted as >20% of the levels reported in healthy human muscle. A review of the dystrophin western blot data on Duchenne and Becker muscular dystrophy biopsies is conducted, along with a thorough investigation of methodologies to quantify dystrophin.

[1]  E. Hoffman,et al.  Report of a TREAT-NMD/World Duchenne Organisation Meeting on Dystrophin Quantification Methodology , 2019, Journal of neuromuscular diseases.

[2]  J. Mendell,et al.  Eteplirsen treatment for Duchenne muscular dystrophy , 2018, Neurology.

[3]  S. Takeda,et al.  Systemic administration of the antisense oligonucleotide NS-065/NCNP-01 for skipping of exon 53 in patients with Duchenne muscular dystrophy , 2018, Science Translational Medicine.

[4]  N. Datson,et al.  Use of capillary Western immunoassay (Wes) for quantification of dystrophin levels in skeletal muscle of healthy controls and individuals with Becker and Duchenne muscular dystrophy , 2018, PloS one.

[5]  E. Mercuri,et al.  D01 Golodirsen induces exon skipping leading to sarcolemmal dystrophin expression in patients with genetic mutations amenable to exon 53 skipping , 2018, Neuromuscular Disorders.

[6]  R. Weiss,et al.  Low-level dystrophin expression attenuating the dystrophinopathy phenotype , 2017, Neuromuscular Disorders.

[7]  S. Wilton,et al.  P.240 Dystrophin expression in the non-DMD population: What is normal? , 2016, Neuromuscular Disorders.

[8]  S. Wilton,et al.  The emperor's new dystrophin: finding sense in the noise. , 2015, Trends in molecular medicine.

[9]  T. Gorr,et al.  Western blotting revisited: Critical perusal of underappreciated technical issues , 2015, Proteomics. Clinical applications.

[10]  F. Muntoni,et al.  Dystrophin quantification , 2014, Neurology.

[11]  C. Farquharson,et al.  A Guide to Modern Quantitative Fluorescent Western Blotting with Troubleshooting Strategies , 2014, Journal of visualized experiments : JoVE.

[12]  C. Beekman,et al.  A Sensitive, Reproducible and Objective Immunofluorescence Analysis Method of Dystrophin in Individual Fibers in Samples from Patients with Duchenne Muscular Dystrophy , 2014, PloS one.

[13]  B. Kholodenko,et al.  Evaluating Strategies to Normalise Biological Replicates of Western Blot Data , 2014, PloS one.

[14]  Annemieke Aartsma-Rus Dystrophin Analysis in Clinical Trials. , 2014, Journal of neuromuscular diseases.

[15]  V. Ricotti,et al.  Biochemical characterization of patients with in-frame or out-of-frame DMD deletions pertinent to exon 44 or 45 skipping. , 2014, JAMA neurology.

[16]  H. Kan,et al.  Dystrophin levels and clinical severity in Becker muscular dystrophy patients , 2013, Journal of Neurology, Neurosurgery & Psychiatry.

[17]  K. Flanigan,et al.  Quantification of dystrophin immunofluorescence in dystrophinopathy muscle specimens , 2012, Neuropathology and applied neurobiology.

[18]  E. Hoffman,et al.  Accurate Quantitation of Dystrophin Protein in Human Skeletal Muscle Using Mass Spectrometry. , 2012, Journal of bioanalysis & biomedicine.

[19]  K. Bushby,et al.  Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials. , 2011, Brain : a journal of neurology.

[20]  J. Bourke,et al.  Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: an open-label, phase 2, dose-escalation study , 2011, The Lancet.

[21]  G. van Ommen,et al.  Systemic administration of PRO051 in Duchenne's muscular dystrophy. , 2011, The New England journal of medicine.

[22]  F. Rivier,et al.  Mutation spectrum leading to an attenuated phenotype in dystrophinopathies , 2005, European Journal of Human Genetics.

[23]  K. Bushby,et al.  Genetic and clinical correlations of Xp21 muscular dystrophy , 1992, Journal of Inherited Metabolic Disease.

[24]  K. Bushby,et al.  The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy , 1993, Journal of Neurology.

[25]  K. Bushby,et al.  The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy , 1993, Journal of Neurology.

[26]  K. Bushby,et al.  Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 3. Differential diagnosis and prognosis. , 1993, Journal of medical genetics.

[27]  R. Waterston,et al.  Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy. , 1988, The New England journal of medicine.