Mitochondrial targeting and therapeutic use thereof
AssigneeShire Human Genetic Therapies, Inc.
InventorsDennis Keefe, Michael Concino, Michael Heartlein, Serene Josiah, Bettina Strack-Logue
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AssigneeShire Human Genetic Therapies, Inc.
InventorsDennis Keefe, Michael Concino, Michael Heartlein, Serene Josiah, Bettina Strack-Logue
Estimating the term…
The present invention provides, among other things, compositions and methods for treatment of Friedrich's Ataxia based on effective targeting of a therapeutic moiety to mitochondria that can substitute for natural FXN protein activity or rescue one or more phenotypes or symptoms associated with frataxin-deficiency. In some embodiments, the present invention provides a targeted therapeutic comprising a therapeutic moiety, which is a polypeptide having an N-terminus and a C-terminus, a mitochondrial targeting sequence associated with the therapeutic moiety at the N-terminus, and a mitochondrial membrane-penetrating peptide associated with the therapeutic moiety at the C-terminus, wherein the therapeutic moiety is targeted to mitochondria upon cellular entry.
A targeted therapeutic comprising
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A targeted therapeutic comprising
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A targeted therapeutic fusion protein comprising an amino acid sequence at least 80% identical to SEQ ID N0:6.
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A method of treating Friedreich's Ataxia comprising administering to a subject in need of treatment a targeted therapeutic comprising a therapeutic moiety, which is a polypeptide having an N-terminus and a C-terminus and having an amino acid sequence at least 80% identical to mature human frataxin protein (SEQ ID NO:
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Dependencies are inferred from the claim text.