An effective method for profiling the selenium-binding proteins using its reactive metabolic intermediate

Verfasser / Beitragende:
[Eriko Hori, Sakura Yoshida, Mamoru Haratake, Sakiko Ura, Takeshi Fuchigami, Morio Nakayama]
Ort, Verlag, Jahr:
2015
Enthalten in:
JBIC Journal of Biological Inorganic Chemistry, 20/5(2015-07-01), 781-789
Format:
Artikel (online)
ID: 605507732
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024 7 0 |a 10.1007/s00775-015-1265-3  |2 doi 
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245 0 3 |a An effective method for profiling the selenium-binding proteins using its reactive metabolic intermediate  |h [Elektronische Daten]  |c [Eriko Hori, Sakura Yoshida, Mamoru Haratake, Sakiko Ura, Takeshi Fuchigami, Morio Nakayama] 
520 3 |a Currently, the intracellular reduction and/or transport of selenium still remain unknown. Certain reduced forms of selenium species are thought to be reactive with various endogenous molecules, particularly thiol-containing proteins. In this study, a profiling method for identifying the selenium-binding proteins using l-penicillamine selenotrisulfide (PenSSeSPen) as a model of the selenium metabolic intermediate was applied to the cell lysate generated from the rat liver. Several proteins with cysteine thiol were found to be reactive with PenSSeSPen through the thiol-exchange reaction by MALDI TOF-MS analysis. The most distinctive cysteine-containing protein at m/z 14,313 in the liver cell lysate was identified as the liver fatty acid-binding protein based on a rat protein database search and a tryptic fragmentation experiment. This methodology could be used for determining the selenium-binding proteins and/or selenium-interactive species and provide a better understanding of the selenium metabolism and utilization in biological systems. 
540 |a SBIC, 2015 
690 7 |a Liver fatty acid-binding protein  |2 nationallicence 
690 7 |a Mass spectrometry  |2 nationallicence 
690 7 |a Selenium  |2 nationallicence 
690 7 |a Selenotrisulfide  |2 nationallicence 
690 7 |a Thiol exchange  |2 nationallicence 
690 7 |a Cys : l-Cysteine  |2 nationallicence 
690 7 |a DAN : 2,3-Diaminonaphthalene  |2 nationallicence 
690 7 |a DTNB : 5,5′-Dithiobis(2-nitrobenzoic acid)  |2 nationallicence 
690 7 |a GPx : Glutathione peroxidase  |2 nationallicence 
690 7 |a GSH : Glutathione in the reduced form  |2 nationallicence 
690 7 |a LFABP : Liver fatty acid-binding protein  |2 nationallicence 
690 7 |a MALDI TOF-MS : Matrix-assisted laser desorption ionization time of flight-mass spectrometry  |2 nationallicence 
690 7 |a NEM : N-Ethylmaleimide  |2 nationallicence 
690 7 |a Pen : L-Penicillamine  |2 nationallicence 
690 7 |a PenSSeSPen : L-Penicillamine selenotrisulfide  |2 nationallicence 
690 7 |a SeCys, Sec and U : l-Selenocysteine  |2 nationallicence 
690 7 |a STS : Selenotrisulfide  |2 nationallicence 
700 1 |a Hori  |D Eriko  |u Graduate School of Biomedical Sciences, Nagasaki University, 1-14 Bunkyo-machi, 852-8521, Nagasaki, Japan  |4 aut 
700 1 |a Yoshida  |D Sakura  |u Graduate School of Biomedical Sciences, Nagasaki University, 1-14 Bunkyo-machi, 852-8521, Nagasaki, Japan  |4 aut 
700 1 |a Haratake  |D Mamoru  |u Faculty of Pharmaceutical Sciences, Sojo University, 4-22-1 Ikeda, 860-0082, Kumamoto, Japan  |4 aut 
700 1 |a Ura  |D Sakiko  |u Graduate School of Biomedical Sciences, Nagasaki University, 1-14 Bunkyo-machi, 852-8521, Nagasaki, Japan  |4 aut 
700 1 |a Fuchigami  |D Takeshi  |u Graduate School of Biomedical Sciences, Nagasaki University, 1-14 Bunkyo-machi, 852-8521, Nagasaki, Japan  |4 aut 
700 1 |a Nakayama  |D Morio  |u Graduate School of Biomedical Sciences, Nagasaki University, 1-14 Bunkyo-machi, 852-8521, Nagasaki, Japan  |4 aut 
773 0 |t JBIC Journal of Biological Inorganic Chemistry  |d Springer Berlin Heidelberg  |g 20/5(2015-07-01), 781-789  |x 0949-8257  |q 20:5<781  |1 2015  |2 20  |o 775 
856 4 0 |u https://doi.org/10.1007/s00775-015-1265-3  |q text/html  |z Onlinezugriff via DOI 
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900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s00775-015-1265-3  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Hori  |D Eriko  |u Graduate School of Biomedical Sciences, Nagasaki University, 1-14 Bunkyo-machi, 852-8521, Nagasaki, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Yoshida  |D Sakura  |u Graduate School of Biomedical Sciences, Nagasaki University, 1-14 Bunkyo-machi, 852-8521, Nagasaki, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Haratake  |D Mamoru  |u Faculty of Pharmaceutical Sciences, Sojo University, 4-22-1 Ikeda, 860-0082, Kumamoto, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Ura  |D Sakiko  |u Graduate School of Biomedical Sciences, Nagasaki University, 1-14 Bunkyo-machi, 852-8521, Nagasaki, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Fuchigami  |D Takeshi  |u Graduate School of Biomedical Sciences, Nagasaki University, 1-14 Bunkyo-machi, 852-8521, Nagasaki, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Nakayama  |D Morio  |u Graduate School of Biomedical Sciences, Nagasaki University, 1-14 Bunkyo-machi, 852-8521, Nagasaki, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t JBIC Journal of Biological Inorganic Chemistry  |d Springer Berlin Heidelberg  |g 20/5(2015-07-01), 781-789  |x 0949-8257  |q 20:5<781  |1 2015  |2 20  |o 775