| Literature DB >> 19967058 |
Kyoung Sun Park1, Hyoweon Bang, Eun-Young Shin, Chan Hyung Kim, Yangmi Kim.
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.Entities:
Keywords: 5,5'-dithio-bis(2-nitrobenzoic acid) (DTNB); C-terminus; K2P; Oxidizing agent; TREK2; Two-pore domain K+ channel; dithiothreitol (DTT)
Year: 2008 PMID: 19967058 PMCID: PMC2788638 DOI: 10.4196/kjpp.2008.12.4.211
Source DB: PubMed Journal: Korean J Physiol Pharmacol ISSN: 1226-4512 Impact factor: 2.016