| First Author | Shimizu T | Year | 2017 |
| Journal | FEBS Open Bio | Volume | 7 |
| Issue | 9 | Pages | 1392-1401 |
| PubMed ID | 28904867 | Mgi Jnum | J:266474 |
| Mgi Id | MGI:6245961 | Doi | 10.1002/2211-5463.12273 |
| Citation | Shimizu T, et al. (2017) The asparagine 533 residue in the outer pore loop region of the mouse PKD2L1 channel is essential for its voltage-dependent inactivation. FEBS Open Bio 7(9):1392-1401 |
| abstractText | Voltage-dependent inactivation of ion channels contributes to the regulation of the membrane potential of excitable cells. Mouse polycystic kidney disease 2-like 1 (PKD2L1) forms voltage-dependent nonselective cation channels, which are activated but subsequently inactivated in response to membrane depolarization. Here, we found that the mutation of an asparagine 533 residue (N533Q) in the outer pore loop region of PKD2L1 caused a marked increase in outward currents induced by depolarization. In addition, the tail current analysis demonstrated that the N533Q mutants are activated during depolarization but the subsequent inactivation does not occur. Interestingly, the N533Q mutants lacked the channel activation triggered by the removal of stimuli such as extracellular alkalization and heating. Our findings suggest that the N533 residue in the outer pore loop region of PKD2L1 has a key role in the voltage-dependent channel inactivation. |
