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PMID:21576493
Citation |
Li, Y, Zaydman, MA, Wu, D, Shi, J, Guan, M, Virgin-Downey, B and Cui, J (2011) KCNE1 enhances phosphatidylinositol 4,5-bisphosphate (PIP2) sensitivity of IKs to modulate channel activity. Proc. Natl. Acad. Sci. U.S.A. 108:9095-100 |
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Abstract |
Phosphatidylinositol 4,5-bisphosphate (PIP(2)) is necessary for the function of various ion channels. The potassium channel, I(Ks), is important for cardiac repolarization and requires PIP(2) to activate. Here we show that the auxiliary subunit of I(Ks), KCNE1, increases PIP(2) sensitivity 100-fold over channels formed by the pore-forming KCNQ1 subunits alone, which effectively amplifies current because native PIP(2) levels in the membrane are insufficient to activate all KCNQ1 channels. A juxtamembranous site in the KCNE1 C terminus is a key structural determinant of PIP(2) sensitivity. Long QT syndrome associated mutations of this site lower PIP(2) affinity, resulting in reduced current. Application of exogenous PIP(2) to these mutants restores wild-type channel activity. These results reveal a vital role of PIP(2) for KCNE1 modulation of I(Ks) channels that may represent a common mechanism of auxiliary subunit modulation of many ion channels. |
Links |
PubMed PMC3107281 Online version:10.1073/pnas.1100872108 |
Keywords |
Amino Acid Sequence; Animals; Humans; Ions; KCNQ1 Potassium Channel/metabolism; Lipids/chemistry; Long QT Syndrome/genetics; Molecular Sequence Data; Mutation; Patch-Clamp Techniques; Phosphatidylinositol 4,5-Diphosphate/metabolism; Potassium Channels/chemistry; Potassium Channels, Voltage-Gated/metabolism; Protein Structure, Tertiary; Sequence Homology, Amino Acid; Xenopus Proteins/metabolism; Xenopus laevis |
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Significance
Annotations
Gene product | Qualifier | GO Term | Evidence Code | with/from | Aspect | Extension | Notes | Status |
---|---|---|---|---|---|---|---|---|
GO:2001259: positive regulation of cation channel activity |
ECO:0000315: |
P |
Fig 2. shows the presence of KCNE1 bound to KCNQ1 increases channel sensitivity of PiP2 and alters the IKs. |
complete | ||||
See also
References
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