z-logo
open-access-imgOpen Access
The Inhibition of TREK2 Channel by an Oxidizing Agent, 5,5'-dithio-bis (2-nitrobenzoic acid), via Interaction with the C-terminus Distal to the 353rd Amino Acid
Author(s) -
Kyoung Sun Park,
Hyoweon Bang,
EunYoung Shin,
Chan Hyung Kim,
Yangmi Kim
Publication year - 2008
Publication title -
korean journal of physiology and pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.514
H-Index - 29
eISSN - 2093-3827
pISSN - 1226-4512
DOI - 10.4196/kjpp.2008.12.4.211
Subject(s) - oxidizing agent , pharmacology , chemistry , amino acid residue , medicine , combinatorial chemistry , biochemistry , peptide sequence , organic chemistry , gene
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.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom