{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,28]],"date-time":"2026-09-28T11:00:51Z","timestamp":1790593251533,"version":"4.1.0"},"reference-count":57,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2026,9,1]],"date-time":"2026-09-01T00:00:00Z","timestamp":1788220800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,9,1]],"date-time":"2026-09-01T00:00:00Z","timestamp":1788220800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["J of Inher Metab Disea"],"published-print":{"date-parts":[[2026,9]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>Aspartylglucosaminuria (AGU) is a lysosomal storage disorder caused by a deficiency of aspartylglucosaminidase (AGA), a hydrolase involved in the degradation of N\u2010glycosylated proteins. Currently, no approved therapies are available for AGU. Development of enzyme replacement therapy (ERT) for AGU has been hampered by the complex proteolytic processing and activation of the AGA enzyme that involves dimerization and cleavage into two subunits. Targeting of AGA into lysosomes is mainly accomplished by a mannose\u20106\u2010phosphate receptor\u2010mediated pathway, and both AGA subunits contain phosphorylated N\u2010glycans. In this study, we have developed an overexpression system for an optimized human AGA enzyme and a truncated GlcNAc\u20101\u2010phosphotransferase, S1S3, that is required for the mannose\u20106\u2010phosphorylation. We here show that the Man\u20106\u2010phosphorylation and cellular uptake of AGA are enhanced by the coexpression of S1S3, and high amounts of affinity\u2010tagged recombinant human AGA can be expressed in HEK293T cells and purified from the culture medium. Impairment of the N\u2010glycosylation of AGA results in poor uptake into cells, indicating that the Man\u20106\u2010dependent route is the main endocytic pathway of AGA. Furthermore, for optimal uptake, both subunits of AGA need to be glycosylated and Man\u20106\u2010phosphorylated. The results of this study enhance the understanding of the lysosomal targeting mechanisms of AGA and pave the way for the development of ERT for AGU.<\/jats:p>","DOI":"10.1002\/jimd.70248","type":"journal-article","created":{"date-parts":[[2026,9,1]],"date-time":"2026-09-01T08:35:19Z","timestamp":1788251719000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Revisiting Enzyme Replacement Therapy for Aspartylglucosaminuria: Truncated Phosphotransferase Enhances Mannose\u20106\u2010Phosphorylation and Cellular Uptake of Aspartylglucosaminidase"],"prefix":"10.1002","volume":"49","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-0196-6996","authenticated-orcid":false,"given":"Antje","family":"Banning","sequence":"first","affiliation":[{"name":"Institute of Biochemistry, Medical Faculty University of Giessen  Giessen 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