Journal
SCIENTIFIC REPORTS
Volume 6, Issue -, Pages -Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/srep27652
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Funding
- NIH [R01NS055159, R01GM093290]
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Phosphatidylinositol 4,5-bisphosphate [PI(4,5)P-2] is an important cofactor for ion channels. Affinity for this lipid is a major determinant of channel inhibition by depletion of PI(4,5)P-2 upon phospholipase C (PLC) activation. Little is known about what determines PI(4,5)P-2 affinity in mammalian ion channels. Here we report that two members of the Transient Receptor Potential Vanilloid (TRPV) ion channel family, TRPV5 and TRPV6 lack a positively charged residue in the TM4-TM5 loop that was shown to interact with PI(4,5)P-2 in TRPV1, which shows high affinity for this lipid. When this positively charged residue was introduced to either TRPV6 or TRPV5, they displayed markedly higher affinities for PI(4,5)P-2, and were largely resistant to inhibition by PI(4,5)P-2 depletion. Furthermore, Ca2+-induced inactivation of TRPV6 was essentially eliminated in the G488R mutant, showing the importance of PLC-mediated PI(4,5)P-2 depletion in this process. Computational modeling shows that the introduced positive charge interacts with PI(4,5)P-2 in TRPV6.
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