Protocol to measure endogenous GlcNAc-1-phosphotransferase activity in SK-MEL-30 cells.

阅读:3
作者:Doray Balraj, Henn Danielle, Yang Xi, Li Ming, Dickson Patricia
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 [(3)H]UDP-GlcNAc donor substrate and conditions for the enzymatic transfer of [(3)H]GlcNAc-1-P to the methyl α-D-mannopyranoside acceptor (α-MM). We then describe the chromatography steps to specifically separate the [(3)H]GlcNAc-1-P-αMM GNPT reaction product from unreacted [(3)H]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).

特别声明

1、本文转载旨在传播信息,不代表本网站观点,亦不对其内容的真实性承担责任。

2、其他媒体、网站或个人若从本网站转载使用,必须保留本网站注明的“来源”,并自行承担包括版权在内的相关法律责任。

3、如作者不希望本文被转载,或需洽谈转载稿费等事宜,请及时与本网站联系。

4、此外,如需投稿,也可通过邮箱info@biocloudy.com与我们取得联系。