期刊
STRUCTURE
卷 28, 期 2, 页码 169-+出版社
CELL PRESS
DOI: 10.1016/j.str.2019.11.005
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资金
- BBSRC
- EPSRC
- Wellcome
- UCB
- AbbVie
- Bayer Pharma AG
- Boehringer Ingelheim
- Canada Foundation for Innovation
- Genome Canada
- Janssen
- Merck KGaA
- Merck
- Novartis
- Ontario Ministry of Economic Development and Innovation
- Pfizer
- Sao Paulo Research Foundation-FAPESP
- Takeda
- Innovative Medicines Initiative Joint Undertaking ULTRA-DD grant [115766]
- Wellcome Trust [106169/Z/14/Z]
- Wellcome Trust
- MRC
- BBRSC
- NIGMS [P41-GM103311]
- Lilly Canada
- BBSRC [BB/R00126X/1, BB/L002558/1] Funding Source: UKRI
- EPSRC [EP/R004722/1, EP/R029407/1] Funding Source: UKRI
Polycystin-2 (PC2) is a transient receptor potential (TRP) channel present in ciliary membranes of the kidney. PC2 shares a transmembrane fold with other TRP channels, in addition to an extracellular domain found in TRPP and TRPML channels. Using molecular dynamics (MD) simulations and cryoelectron microscopy we identify and characterize PIP2 and cholesterol interactions with PC2. PC2 is revealed to have a PIP binding site close to the equivalent vanilloid/lipid binding site in the TRPV1 channel. A 3.0-angstrom structure reveals a binding site for cholesterol on PC2. Cholesterol interactions with the channel at this site are characterized by MD simulations. The two classes of lipid binding sites are compared with sites observed in other TRPs and in Kv channels. These findings suggest PC2, in common with other ion channels, may be modulated by both PIPs and cholesterol, and position PC2 within an emerging model of the roles of lipids in the regulation and organization of ciliary membranes.
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