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-Structure paper
タイトル | Anionic lipids unlock the gates of select ion channels in the pacemaker family. |
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ジャーナル・号・ページ | Nat Struct Mol Biol, Vol. 29, Issue 11, Page 1092-1100, Year 2022 |
掲載日 | 2022年11月9日 |
著者 | Philipp A M Schmidpeter / Di Wu / Jan Rheinberger / Paul M Riegelhaupt / Haiping Tang / Carol V Robinson / Crina M Nimigean / |
PubMed 要旨 | Lipids play important roles in regulating membrane protein function, but the molecular mechanisms used are elusive. Here we investigated how anionic lipids modulate SthK, a bacterial pacemaker ...Lipids play important roles in regulating membrane protein function, but the molecular mechanisms used are elusive. Here we investigated how anionic lipids modulate SthK, a bacterial pacemaker channel homolog, and HCN2, whose activity contributes to pacemaking in the heart and brain. Using SthK allowed the reconstitution of purified channels in controlled lipid compositions for functional and structural assays that are not available for the eukaryotic channels. We identified anionic lipids bound tightly to SthK and their exact binding locations and determined that they potentiate channel activity. Cryo-EM structures in the most potentiating lipids revealed an open state and identified a nonannular lipid bound with its headgroup near an intersubunit salt bridge that clamps the intracellular channel gate shut. Breaking this conserved salt bridge abolished lipid modulation in SthK and eukaryotic HCN2 channels, indicating that anionic membrane lipids facilitate channel opening by destabilizing these interactions. Our findings underline the importance of state-dependent protein-lipid interactions. |
リンク | Nat Struct Mol Biol / PubMed:36352139 / PubMed Central |
手法 | EM (単粒子) |
解像度 | 2.41 - 3.6 Å |
構造データ | EMDB-25916, PDB-7tj5: EMDB-25917, PDB-7tj6: EMDB-25981, PDB-7tkt: |
化合物 | ChemComp-CMP: ChemComp-D21: ChemComp-PGW: |
由来 |
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キーワード | TRANSPORT PROTEIN / cyclic nucleotide-gated channel / lipid modulation / pacemaker channel |