Determination of protein phosphorylation and the translocation of green fluorescence protein-extracellular signal-regulated kinase 2 by capillary electrophoresis using laser induced fluorescence detection

Authors
Yoon, SHan, KYNam, HSNga, LVYoo, YS
Issue Date
2004-11-12
Publisher
ELSEVIER SCIENCE BV
Citation
JOURNAL OF CHROMATOGRAPHY A, v.1056, no.1-2, pp.237 - 242
Abstract
In this study, we developed a method to monitor the phosphorylation and translocation of the extracellular signal-regulated kinase (ERK2) proteins after PC12 cells have been stimulated by a mitogen. The method involves the use of green fluorescent protein (GFP), capillary electrophoresis and the measurement of laser-induced fluorescence (CE-LIF). We showed the prescence of the non-phosphorylated GFP-ERK2 and phosphorylated GFP-ERK2 in cell lysates by CE-LIF, and then compared the phosphorylations of GFP-ERK2 and GFP-183A. Phosphorylated GFP-ERK2 was detected at 6.7 min and the non-phosphorylated GFP-ERK2 at 5.3-5.5 min. The results were compared with confocal laser scanning microscope imaging and western blot results, and suggest that the developed method can be used to detect other enzymatic modifications. (C) 2004 Elsevier B.V. All rights reserved.
Keywords
NERVE GROWTH-FACTOR; PC12 CELLS; PHEOCHROMOCYTOMA CELLS; PHOSPHOLIPASE A(2); COMPLEX-FORMATION; FUSION PROTEIN; ACTIVATION; EXPRESSION; STIMULATION; INVOLVEMENT; NERVE GROWTH-FACTOR; PC12 CELLS; PHEOCHROMOCYTOMA CELLS; PHOSPHOLIPASE A(2); COMPLEX-FORMATION; FUSION PROTEIN; ACTIVATION; EXPRESSION; STIMULATION; INVOLVEMENT; protein phosphorylation; extracellular signal-regulated kinase; enzymes; green fluorescent protein
ISSN
0021-9673
URI
https://pubs.kist.re.kr/handle/201004/137059
DOI
10.1016/j.chroma.2004.06.109
Appears in Collections:
KIST Article > 2004
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