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The inhibition of TREK2 channel by an oxidizing agent, 5,5 '-dithiobis (2-nitrobenzoic acid), via interaction with the c-terminus distal to the 353rd amino acidopen access

Authors
Park, Kyoung SunBang, HyoweonShin, Eun-YoungKim, Chan HyungKim, Yangmi
Issue Date
Aug-2008
Publisher
KOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY
Keywords
TREK2; oxidizing agent; 5,5 '-dithio-bis(2-nitrobenzoic acid) (DTNB); dithiothreitol (DTT); C-terminus; two-pore domain K+ channel; K-2P
Citation
KOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY, v.12, no.4, pp 211 - 216
Pages
6
Journal Title
KOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY
Volume
12
Number
4
Start Page
211
End Page
216
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/23660
DOI
10.4196/kjpp.2008.12.4.211
ISSN
1226-4512
2093-3827
Abstract
TREK (TWIK-RElated K+ channels) and TRAAK (TWIK-Related Arachidonic acid Activated K+ channels) were expressed in COS-7 cells, and the channel activities were recorded from inside-out membrane patches using holding potential of -40 mV in symmetrical 150 mM K+ solution. Intracellular application of an oxidizing agent, 5,5'-dithio-bis (2-nitrobenzoic acid) (DTNB), markedly decreased the activity of the TREK2, and the activity was partially reversed by the reducing agent, dithiothreitol (DTT). In order to examine the possibility that the target sites for the oxidizing agents might be located in the C-terminus of TREK2, two chimeras were constructed: TREK2 (1-383)/TASK3C and TREK2 (1-353)/TASK3C. The channel activity in the TREK2 (1-383)/TASK3C chimera was still inhibited by DTNB, but not in the TREK2 (1-353)/TASK3C chimera. These results indicate that TREK2 is inhibited by oxidation, and that the target site for oxidation is located between the amino acid residues 353 and 383 in the C-terminus of the TREK2 protein.
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