Molecular characterization of membrane type and ganglioside-specific sialidase (Neu3) expressed in E. coli

• Published in: Molecules and cells Vol. 17; no. 2; pp. 267 - 273
• Main Authors: Ha, Ki-Tae, Lee, Young-Choon, Cho, Seung-Hak, Kim, June-Ki, Kim, Cheorl-Ho
• Format: Journal Article
• Language: English
• Published: United States 30.04.2004
• Subjects: Amino Acid Sequence; Base Sequence; Cell Line; Escherichia coli - genetics; Escherichia coli - metabolism; Gangliosides - metabolism; Humans; Hydrogen-Ion Concentration; Hymecromone - analogs & derivatives; Hymecromone - metabolism; Molecular Sequence Data; Neuraminidase - chemistry; Neuraminidase - genetics; Neuraminidase - isolation & purification; Neuraminidase - metabolism; Recombinant Proteins - isolation & purification; Recombinant Proteins - metabolism
• ISSN: 1016-8478
• DOI: 10.1016/s1016-8478(23)13037-8

Endogenous expression of human membrane type ganglioside sialidase (Neu3) was examined in various cell lines including NB-1, U87MG, SK-MEL-2, SK-N-MC, HepG2, Hep3B, Jurkat, HL-60, K562, ECV304, Hela and MCF-7. Expression was detected in the neuroblastoma cell lines NB-1 and SK-N-MC, and also in erythroleukemia K562 cells, but not in any other cells. We isolated a Neu3 cDNA from K562 cells and expressed a His-tagged derivative in a bacterial expression system. The purified recombinant product of approximately 48 kDa had sialidase activity toward 4-methyl-umbelliferyl-alpha-D-N-acetylneuraminic acid (4MU-NeuAc). The optimal pH of the purified Neu3 protein for GD3 ganglioside was 4.5. The enzyme also efficiently hydrolyzed GD3, GD1a, GD1b and GM3 whereas sialyllactose, 4MU-NeuAc, GM1 and GM2 were poor substrates, and it had no activity against sialylated glycoproteins such as fetuin, transferrin and orosomucoid. We conclude that the sialidase activity of Neu3 is specific for gangliosides.