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-Structure paper
タイトル | Structural insights into GIRK2 channel modulation by cholesterol and PIP. |
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ジャーナル・号・ページ | Cell Rep, Vol. 36, Issue 8, Page 109619, Year 2021 |
掲載日 | 2021年8月24日 |
著者 | Yamuna Kalyani Mathiharan / Ian W Glaaser / Yulin Zhao / Michael J Robertson / Georgios Skiniotis / Paul A Slesinger / |
PubMed 要旨 | G-protein-gated inwardly rectifying potassium (GIRK) channels are important for determining neuronal excitability. In addition to G proteins, GIRK channels are potentiated by membrane cholesterol, ...G-protein-gated inwardly rectifying potassium (GIRK) channels are important for determining neuronal excitability. In addition to G proteins, GIRK channels are potentiated by membrane cholesterol, which is elevated in the brains of people with neurodegenerative diseases such as Alzheimer's dementia and Parkinson's disease. The structural mechanism of cholesterol modulation of GIRK channels is not well understood. In this study, we present cryo- electron microscopy (cryoEM) structures of GIRK2 in the presence and absence of the cholesterol analog cholesteryl hemisuccinate (CHS) and phosphatidylinositol 4,5-bisphosphate (PIP). The structures reveal that CHS binds near PIP in lipid-facing hydrophobic pockets of the transmembrane domain. Our structural analysis suggests that CHS stabilizes PIP interaction with the channel and promotes engagement of the cytoplasmic domain onto the transmembrane region. Mutagenesis of one of the CHS binding pockets eliminates cholesterol-dependent potentiation of GIRK2. Elucidating the structural mechanisms underlying cholesterol modulation of GIRK2 channels could facilitate the development of therapeutics for treating neurological diseases. VIDEO ABSTRACT. |
リンク | Cell Rep / PubMed:34433062 / PubMed Central |
手法 | EM (単粒子) |
解像度 | 3.2 - 7.7 Å |
構造データ | EMDB-22150, PDB-6xeu: EMDB-22151: EMDB-22152: EMDB-22153: EMDB-22154, PDB-6xev: EMDB-22155: |
化合物 | ChemComp-PIO: ChemComp-K: ChemComp-NA: ChemComp-Y01: |
由来 |
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キーワード | TRANSPORT PROTEIN / GIRK / inwardly rectifying potassium channel / cholesterol / lipids / PIP2 / CryoEM |