Analysis of mannose-6-phosphate labeled with 8-aminopyrene-1,3,6- trisulfonate by capillary electrophoresis

Analytical Biochemistry

Volumn 332, Issue 1, 2004, Pages 196-198

  Takashiba, Minako ^a   Chiba, Yasunori ^a   Arai, Etsuo ^b   Jigami, Yoshifumi ^a  

^a NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY AIST   (Japan)

^b BECKMAN COULTER INC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BIOCHEMISTRY; CHEMISTRY;

MANNOSE 6 PHOSPHATES;

CAPILLARY ELECTROPHORESIS;

8 AMINOPYRENE 1,3,6 TRISULFONATE; BORIC ACID; BUFFER; MANNOSE 6 PHOSPHATE; SULFONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

AMPEROMETRIC BIOSENSOR; ARTICLE; CAPILLARY ELECTROPHORESIS; CARBOHYDRATE ANALYSIS; CELL LABELING; CHEMICAL STRUCTURE; ENZYME ACTIVATION; ENZYME ACTIVITY; FLUORESCENCE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; LASER; PRIORITY JOURNAL; SEPARATION TECHNIQUE; STRUCTURE ANALYSIS; TEMPERATURE DEPENDENCE;

EID: 4143119035     PISSN: 00032697     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ab.2004.05.049     Document Type: Article

References (7)

1. Dahms N.M., Lobel P., Kornfeld S. Mannose 6-phosphate receptors and lysosomal enzyme targeting. J. Biol. Chem. 264:1989;12115-12118
2. Lee K., Jin X., Zhang K., Copertino L., Andrews L., Baker-Malcolm J., Geagan L., Qiu H., Seiger K., Barngrover D., Mcpherson J.M., Edmunds T. A biochemical and pharmacological comparison of enzyme replacement therapies for the glycolipid storage disorder Fabry disease. Glycobiology. 13:2003;305-313
3. Chen F.T.A., Dobashi T.S., Evangelista R.A. Quantitative analysis of sugar constituents of glycoproteins by capillary electrophoresis. Glycobiology. 8:1998;1045-1052
4. Chen F.T.A., Evangelista R.A. Analysis of mono- and oligosaccharide isomers derivatized with 9-aminopyrene-1,4,6-trisulfonate by capillary electrophoresis with laser- induced fluorescence. Anal. Biochem. 230:1995;273-280
5. Hanko V.P., Rohrer J.S. Determination of carbohydrates, sugar alchols, and glycols in cell cultures and fermentation broths using high performance anion- exchange chromatography with pulsed amperometric detection. Anal. Biochem. 283:2000;192-199
6. Schiffmann R., Murray G.J., Treco D., Daniel P., Sellos-Moura M., Myers M., Quirk J.M., Zirzow G.C., Borowski M., Loveday K., Anderson T., Gillespie F., Oliver K.L., Jeffries N.O., Doo E., Liang T.J., Kreps C., gunter K., Frei K., Crutchfield K., Selden R.F., Brady R.O. Infusion of α-galactosidase A reduces tissue globotriaosylceramide storage in patients with Fabry disease. Proc. Natl. Acad. Sci. USA. 97:1999;365-370
7. Chiba Y., Sakuraba H., Kotani M., Kase R., Kobayashi K., Takeuchi M., Ogasawara S., Maruyama Y., Nakajima T., Takaoka Y., Jigami Y. Production in yeast of α-galactosidase A, a lysosomal enzyme applicable to replacement therapy for Fabry disease. Glycobiology. 12:2002;821-828