TY - JOUR
T1 - Role of the KcsA channel cytoplasmic domain in pH-dependent gating
AU - Hirano, Minako
AU - Onishi, Yukiko
AU - Yanagida, Toshio
AU - Ide, Toru
N1 - Funding Information:
This work was supported by a Grant-in-Aid for Scientific Research on Innovative Areas “Fluorescence Live Imaging” (No. 23113519) and “Fluctuations toward Biological Functions” (No. 21107518), for Scientific Research B (No. 22370059) and for Young Scientists B (No. 23770190) of The Ministry of Education, Culture, Sports, Science, and Technology, Japan.
PY - 2011
Y1 - 2011
N2 - The KcsA channel is a representative potassium channel that is activated by changes in pH. Previous studies suggested that the region that senses pH is entirely within its transmembrane segments. However, we recently revealed that the cytoplasmic domain also has an important role, because its conformation was observed to change dramatically in response to pH changes. Here, to investigate the effects of the cytoplasmic domain on pH-dependent gating, we made a chimera mutant channel consisting of the cytoplasmic domain of the KcsA channel and the transmembrane region of the MthK channel. The chimera showed a pH dependency similar to that of KcsA, indicating that the cytoplasmic domain can act as a pH sensor. To identify how this region detects pH, we substituted certain cytoplasmic domain amino acids that are normally negatively charged at pH 7 for neutral ones in the KcsA channels. These mutants opened independently of pH, suggesting that electrostatic charges have a major role in the cytoplasmic domain's ability to sense and respond to pH.
AB - The KcsA channel is a representative potassium channel that is activated by changes in pH. Previous studies suggested that the region that senses pH is entirely within its transmembrane segments. However, we recently revealed that the cytoplasmic domain also has an important role, because its conformation was observed to change dramatically in response to pH changes. Here, to investigate the effects of the cytoplasmic domain on pH-dependent gating, we made a chimera mutant channel consisting of the cytoplasmic domain of the KcsA channel and the transmembrane region of the MthK channel. The chimera showed a pH dependency similar to that of KcsA, indicating that the cytoplasmic domain can act as a pH sensor. To identify how this region detects pH, we substituted certain cytoplasmic domain amino acids that are normally negatively charged at pH 7 for neutral ones in the KcsA channels. These mutants opened independently of pH, suggesting that electrostatic charges have a major role in the cytoplasmic domain's ability to sense and respond to pH.
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U2 - 10.1016/j.bpj.2011.09.024
DO - 10.1016/j.bpj.2011.09.024
M3 - Article
C2 - 22067153
AN - SCOPUS:80455155192
SN - 0006-3495
VL - 101
SP - 2157
EP - 2162
JO - Biophysical Journal
JF - Biophysical Journal
IS - 9
ER -