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Strategy for Treating Motor Neuron Diseases Using a Fusion Protein of Botulinum Toxin Binding Domain and Streptavidin for Viral Vector Access: Work in Progress

1
Department of Neurology, Johns Hopkins School of Medicine, 600 North Wolfe Ave, Baltimore, MD 21287, USA
2
Sirnaomics, Inc., 401 Professional Dr. Suite 130, Gaithersburg, MD 20879, USA
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Author to whom correspondence should be addressed.
Toxins 2010, 2(12), 2872-2889; https://doi.org/10.3390/toxins2122872
Received: 11 October 2010 / Revised: 16 December 2010 / Accepted: 17 December 2010 / Published: 20 December 2010
(This article belongs to the Special Issue Toxins as Therapeutics)
Although advances in understanding of the pathogenesis of amyotrophic lateral sclerosis (ALS) and spinal muscular atrophy (SMA) have suggested attractive treatment strategies, delivery of agents to motor neurons embedded within the spinal cord is problematic. We have designed a strategy based on the specificity of botulinum toxin, to direct entry of viral vectors carrying candidate therapeutic genes into motor neurons. We have engineered and expressed fusion proteins consisting of the binding domain of botulinum toxin type A fused to streptavidin (SAv). This fusion protein will direct biotinylated viral vectors carrying therapeutic genes into motor nerve terminals where they can enter the acidified endosomal compartments, be released and undergo retrograde transport, to deliver the genes to motor neurons. Both ends of the fusion proteins are shown to be functionally intact. The binding domain end binds to mammalian nerve terminals at neuromuscular junctions, ganglioside GT1b (a target of botulinum toxin), and a variety of neuronal cells including primary chick embryo motor neurons, N2A neuroblastoma cells, NG108-15 cells, but not to NG CR72 cells, which lack complex gangliosides. The streptavidin end binds to biotin, and to a biotinylated Alexa 488 fluorescent tag. Further studies are in progress to evaluate the delivery of genes to motor neurons in vivo, by the use of biotinylated viral vectors. View Full-Text
Keywords: botulinum toxin; binding domain; motor neuron diseases; ALS; SMA; motor neurons; therapeutic targeting; gene transfer; viral vectors botulinum toxin; binding domain; motor neuron diseases; ALS; SMA; motor neurons; therapeutic targeting; gene transfer; viral vectors
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MDPI and ACS Style

Drachman, D.B.; Adams, R.N.; Balasubramanian, U.; Lu, Y. Strategy for Treating Motor Neuron Diseases Using a Fusion Protein of Botulinum Toxin Binding Domain and Streptavidin for Viral Vector Access: Work in Progress. Toxins 2010, 2, 2872-2889. https://doi.org/10.3390/toxins2122872

AMA Style

Drachman DB, Adams RN, Balasubramanian U, Lu Y. Strategy for Treating Motor Neuron Diseases Using a Fusion Protein of Botulinum Toxin Binding Domain and Streptavidin for Viral Vector Access: Work in Progress. Toxins. 2010; 2(12):2872-2889. https://doi.org/10.3390/toxins2122872

Chicago/Turabian Style

Drachman, Daniel B., Robert N. Adams, Uma Balasubramanian, and Yang Lu. 2010. "Strategy for Treating Motor Neuron Diseases Using a Fusion Protein of Botulinum Toxin Binding Domain and Streptavidin for Viral Vector Access: Work in Progress" Toxins 2, no. 12: 2872-2889. https://doi.org/10.3390/toxins2122872

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