Direct analysis of retinal dehydrogenase activity on an electroblotting membrane following separation by non-denaturing two-dimensional electrophoresis
被引:1
|
作者:
Shimazaki, Youji
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机构:
Ehime Univ, Grad Sch Sci & Engn, Sci Sect, Venture Business Labs, Matsuyama, Ehime 790, JapanEhime Univ, Grad Sch Sci & Engn, Sci Sect, Venture Business Labs, Matsuyama, Ehime 790, Japan
Shimazaki, Youji
[1
]
Kuroda, Takahiro
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h-index: 0
机构:
Ehime Univ, Grad Sch Sci & Engn, Sci Sect, Venture Business Labs, Matsuyama, Ehime 790, JapanEhime Univ, Grad Sch Sci & Engn, Sci Sect, Venture Business Labs, Matsuyama, Ehime 790, Japan
Kuroda, Takahiro
[1
]
机构:
[1] Ehime Univ, Grad Sch Sci & Engn, Sci Sect, Venture Business Labs, Matsuyama, Ehime 790, Japan
retinal dehydrogenase;
retinal;
retinoic acid;
identification;
de novo sequencing;
D O I:
10.1016/j.jchromb.2007.10.028
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
The reaction from retinal to retinoic acid catalyzed by retinal dehydrogenase on a polyvinylidene difluoride (PVDF) membrane was examined using laser desorption ionization time of flight mass spectrometry (LDI-TOF MS) when the enzyme was separated by non-denaturing two-dimensional electrophoresis (2-DE), transferred onto the membrane, and stained without impairing the enzyme activity. Furthermore, the enzyme was analyzed by de novo sequencing using electrospray ionization tandem mass spectrometry (ESI-MS/MS) after proteins from mouse liver were separated by non-denaturing 2-DE, blotted onto the membrane, and stained. The results indicated that the reported methods could be applied for the direct examination of changes in retinoid catalyzed by enzymes on such membranes. (C) 2007 Elsevier B.V. All rights reserved.