Lactocerebrosides from bovine brain

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CAS: 4682-48-8
MF: C53H101NO13
MW: 960.36794
Synonyms: Lactocerebrosides from bovine brain

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Yu Bai

Peking University
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Huwei Liu

Peking University
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YiSu Jin

Central South University
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Jian Zhu

Soochow University
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Steven R. Tannenbaum

Massachusetts Institute of Technology
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Michael Edidin

Johns Hopkins University
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Donald P. Land

University of California-Davis
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Carlito B. Lebrilla

University of California
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Norman J. Dovichi

The University of Notre Dame
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Co-reporter: Richard B. Keithley, Mark P. Metzinger, Andrea M. Rosado, Norman J. Dovichi
pp: 206-214
Publication Date(Web):15 July 2013
DOI: 10.1016/j.talanta.2013.03.012
► Fluorescent glycosphingolipids from single cells were analyzed by CE-LIF.► Ionic strength modification improved single cell electrophoretic separations.► The enhanced resolution identified new metabolic products previously unrecorded.A capillary electrophoresis system with ultrasensitive two-color laser-induced fluorescence detection was used to probe the effect of ionic strength on single cell separations of glycosphingolipids. Differentiated PC12 cells were incubated with two ganglioside substrates tagged with different fluorophores within the BODIPY family such that two distinct metabolic patterns could be simultaneously monitored. Aspiration of single differentiated PC12 cells suspended in a phosphate-buffered saline solution showed excessive peak dispersion, poor resolution, and peak efficiencies below 100,000 theoretical plates. Aspiration of single differentiated PC12 cells suspended in deionized water corrected peak dispersion. Average peak efficiencies ranged between 400,000 and 600,000 theoretical plates. Improved performance was due to the dilution of the high salt concentrations inside of single neuronal-like cells to produce field amplified sample stacking. Single cell separations showed the highest resolution when aspiration of single differentiated PC12 cells suspended in deionized water were separated using a running buffer of high ionic strength. The improvement in resolution allowed for the identification of analytes not previously detected in single cell metabolism studies.

Amanda B. Hummon

University of Notre Dame
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