Abstract

GlcNAc-1-phosphotransferase (GNPT) is the key enzyme for tagging lysosomal hydrolases with the mannose 6-phosphate moiety for delivery to the lysosome. Here, we present the assay for measuring endogenous GNPT activity in SK-MEL-30 cells. We provide details for preparing the [3H]UDP-GlcNAc donor substrate and conditions for the enzymatic transfer of [3H]GlcNAc-1-P to the methyl α-D-mannopyranoside acceptor (α-MM). We then describe the chromatography steps to specifically separate the [3H]GlcNAc-1-P-αMM GNPT reaction product from unreacted [3H]UDP-GlcNAc that is bound to the quaternary aminoethyl (QAE) Sephadex A-25 matrix. For complete details on the use and execution of this protocol, please refer to Doray et al.1 and Yang et al.2

Original languageEnglish
Article number103935
JournalSTAR Protocols
Volume6
Issue number3
DOIs
StatePublished - Sep 19 2025

Keywords

  • Cell Biology
  • Molecular Biology
  • Protein Biochemistry

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