Promiscuous gating modifiers target the voltage sensor of Kv7.2, TRPV1, and Hv1 cation channels. Issue 6 (5th March 2014)
- Record Type:
- Journal Article
- Title:
- Promiscuous gating modifiers target the voltage sensor of Kv7.2, TRPV1, and Hv1 cation channels. Issue 6 (5th March 2014)
- Main Title:
- Promiscuous gating modifiers target the voltage sensor of Kv7.2, TRPV1, and Hv1 cation channels
- Authors:
- Kornilov, Polina
Peretz, Asher
Lee, Yoonji
Son, Karam
Lee, Jin Hee
Refaeli, Bosmat
Roz, Netta
Rehavi, Moshe
Choi, Sun
Attali, Bernard - Abstract:
- ABSTRACT: Some of the fascinating features of voltage‐sensing domains (VSDs) in voltage‐gated cation channels (VGCCs) are their modular nature and adaptability. Here we examined the VSD sensitivity of different VGCCs to 2 structurally related nontoxin gating modifiers, NH17 and NH29, which stabilize Kv 7.2 potassium channels in the closed and open states, respectively. The effects of NH17 and NH29 were examined in Chinese hamster ovary cells transfected with transient receptor potential vanilloid 1 (TRPV1) or Kv 7.2 channels, as well as in dorsal root ganglia neurons, using the whole‐cell patch‐clamp technique. NH17 and NH29 exert opposite effects on TRPV1 channels, operating, respectively, as an activator and a blocker of TRPV1 currents (EC50 and IC50 values ranging from 4 to 40 μM). Combined mutagenesis, electrophysiology, structural homology modeling, molecular docking, and molecular dynamics simulation indicate that both compounds target the VSDs of TRPV1 channels, which, like vanilloids, are involved in π‐π stacking, H‐bonding, and hydrophobic interactions. Reflecting their promiscuity, the drugs also affect the lone VSD proton channel mV‐SOP. Thus, the same gating modifier can promiscuously interact with different VGCCs, and subtle differences at the VSD‐ligand interface will dictate whether the gating modifier stabilizes channels in either the closed or the open state.—Kornilov, P., Peretz, A., Lee, Y., Son, K., Lee, J. H., Refaeli, B., Roz, N., Rehavi, M., Choi, S.,ABSTRACT: Some of the fascinating features of voltage‐sensing domains (VSDs) in voltage‐gated cation channels (VGCCs) are their modular nature and adaptability. Here we examined the VSD sensitivity of different VGCCs to 2 structurally related nontoxin gating modifiers, NH17 and NH29, which stabilize Kv 7.2 potassium channels in the closed and open states, respectively. The effects of NH17 and NH29 were examined in Chinese hamster ovary cells transfected with transient receptor potential vanilloid 1 (TRPV1) or Kv 7.2 channels, as well as in dorsal root ganglia neurons, using the whole‐cell patch‐clamp technique. NH17 and NH29 exert opposite effects on TRPV1 channels, operating, respectively, as an activator and a blocker of TRPV1 currents (EC50 and IC50 values ranging from 4 to 40 μM). Combined mutagenesis, electrophysiology, structural homology modeling, molecular docking, and molecular dynamics simulation indicate that both compounds target the VSDs of TRPV1 channels, which, like vanilloids, are involved in π‐π stacking, H‐bonding, and hydrophobic interactions. Reflecting their promiscuity, the drugs also affect the lone VSD proton channel mV‐SOP. Thus, the same gating modifier can promiscuously interact with different VGCCs, and subtle differences at the VSD‐ligand interface will dictate whether the gating modifier stabilizes channels in either the closed or the open state.—Kornilov, P., Peretz, A., Lee, Y., Son, K., Lee, J. H., Refaeli, B., Roz, N., Rehavi, M., Choi, S., Attali, B. Promiscuous gating modifiers target the voltage sensor of Kv 7.2, TRPV1, and Hv 1 cation channels. FASEB J . 28, 2591–2602 (2014). www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 28:Issue 6(2014)
- Journal:
- FASEB journal
- Issue:
- Volume 28:Issue 6(2014)
- Issue Display:
- Volume 28, Issue 6 (2014)
- Year:
- 2014
- Volume:
- 28
- Issue:
- 6
- Issue Sort Value:
- 2014-0028-0006-0000
- Page Start:
- 2591
- Page End:
- 2602
- Publication Date:
- 2014-03-05
- Subjects:
- vanilloid -- capsaicin -- KCNQ
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.14-250647 ↗
- Languages:
- English
- ISSNs:
- 0892-6638
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13221.xml