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- W3099543027 abstract "We show the successful application of ancestral sequence reconstruction to enhance the activity of iduronate-2-sulfatase (IDS), thereby increasing its therapeutic potential for the treatment of Hunter syndrome—a lysosomal storage disease caused by impaired function of IDS. Current treatment, enzyme replacement therapy with recombinant human IDS, does not alleviate all symptoms, and an unmet medical need remains. We reconstructed putative ancestral sequences of mammalian IDS and compared them with extant IDS. Some ancestral variants displayed up to 2-fold higher activity than human IDS in in vitro assays and cleared more substrate in ex vivo experiments in patient fibroblasts. This could potentially allow for lower dosage or enhanced therapeutic effect in enzyme replacement therapy, thereby improving treatment outcomes and cost efficiency, as well as reducing treatment burden. In summary, we showed that ancestral sequence reconstruction can be applied to lysosomal enzymes that function in concert with modern enzymes and receptors in cells." @default.
- W3099543027 created "2020-11-23" @default.
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- W3099543027 date "2021-03-01" @default.
- W3099543027 modified "2023-10-12" @default.
- W3099543027 title "Ancestral lysosomal enzymes with increased activity harbor therapeutic potential for treatment of Hunter syndrome" @default.
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- W3099543027 doi "https://doi.org/10.1016/j.isci.2021.102154" @default.
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