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データを開く
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基本情報
| 登録情報 | データベース: PDB / ID: 8yrg | |||||||||||||||||||||||||||||||||||||||
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| タイトル | CryoEM structure of fospropofol-bound MRGPRX4-Gq complex | |||||||||||||||||||||||||||||||||||||||
要素 |
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キーワード | SIGNALING PROTEIN / GPCR-G protein complex | |||||||||||||||||||||||||||||||||||||||
| 機能・相同性 | 機能・相同性情報G protein-coupled bile acid receptor activity / sensory perception of itch / electron transport chain / G protein-coupled receptor activity / Olfactory Signaling Pathway / Activation of the phototransduction cascade / G protein-coupled acetylcholine receptor signaling pathway / G beta:gamma signalling through PLC beta / Presynaptic function of Kainate receptors / Thromboxane signalling through TP receptor ...G protein-coupled bile acid receptor activity / sensory perception of itch / electron transport chain / G protein-coupled receptor activity / Olfactory Signaling Pathway / Activation of the phototransduction cascade / G protein-coupled acetylcholine receptor signaling pathway / G beta:gamma signalling through PLC beta / Presynaptic function of Kainate receptors / Thromboxane signalling through TP receptor / Activation of G protein gated Potassium channels / Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits / G-protein activation / Glucagon signaling in metabolic regulation / G beta:gamma signalling through CDC42 / Prostacyclin signalling through prostacyclin receptor / G beta:gamma signalling through BTK / Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) / photoreceptor disc membrane / ADP signalling through P2Y purinoceptor 12 / Sensory perception of sweet, bitter, and umami (glutamate) taste / Glucagon-type ligand receptors / Adrenaline,noradrenaline inhibits insulin secretion / Vasopressin regulates renal water homeostasis via Aquaporins / Glucagon-like Peptide-1 (GLP1) regulates insulin secretion / G alpha (z) signalling events / cellular response to catecholamine stimulus / ADP signalling through P2Y purinoceptor 1 / ADORA2B mediated anti-inflammatory cytokines production / G beta:gamma signalling through PI3Kgamma / adenylate cyclase-activating dopamine receptor signaling pathway / Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding / GPER1 signaling / cellular response to prostaglandin E stimulus / heterotrimeric G-protein complex / G alpha (12/13) signalling events / Inactivation, recovery and regulation of the phototransduction cascade / G-protein beta-subunit binding / extracellular vesicle / sensory perception of taste / Thrombin signalling through proteinase activated receptors (PARs) / signaling receptor complex adaptor activity / retina development in camera-type eye / GTPase binding / fibroblast proliferation / Ca2+ pathway / High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells / G alpha (i) signalling events / G alpha (s) signalling events / phospholipase C-activating G protein-coupled receptor signaling pathway / G alpha (q) signalling events / Ras protein signal transduction / periplasmic space / electron transfer activity / cell population proliferation / Extra-nuclear estrogen signaling / iron ion binding / G protein-coupled receptor signaling pathway / lysosomal membrane / GTPase activity / heme binding / synapse / protein-containing complex binding / signal transduction / extracellular exosome / membrane / plasma membrane / cytoplasm / cytosol 類似検索 - 分子機能 | |||||||||||||||||||||||||||||||||||||||
| 生物種 | Homo sapiens (ヒト)![]() | |||||||||||||||||||||||||||||||||||||||
| 手法 | 電子顕微鏡法 / 単粒子再構成法 / クライオ電子顕微鏡法 / 解像度: 3.14 Å | |||||||||||||||||||||||||||||||||||||||
データ登録者 | Cao, C. / Fay, J.F. / Roth, B.L. | |||||||||||||||||||||||||||||||||||||||
| 資金援助 | 米国, 2件
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引用 | ジャーナル: Sci Transl Med / 年: 2024タイトル: MRGPRX4 mediates phospho-drug-associated pruritus in a humanized mouse model. 著者: Daphne Chun-Che Chien / Nathachit Limjunyawong / Can Cao / James Meixiong / Qi Peng / Cheng-Ying Ho / Jonathan F Fay / Bryan L Roth / Xinzhong Dong / ![]() 要旨: The phosphate modification of drugs is a common chemical strategy to increase solubility and allow for parenteral administration. Unfortunately, phosphate modifications often elicit treatment- or ...The phosphate modification of drugs is a common chemical strategy to increase solubility and allow for parenteral administration. Unfortunately, phosphate modifications often elicit treatment- or dose-limiting pruritus through an unknown mechanism. Using unbiased high-throughput drug screens, we identified the Mas-related G protein-coupled receptor X4 (MRGPRX4), a primate-specific, sensory neuron receptor previously implicated in itch, as a potential target for phosphate-modified compounds. Using both G-mediated calcium mobilization and G protein-independent GPCR assays, we found that phosphate-modified compounds potently activate MRGPRX4. Furthermore, a humanized mouse model expressing MRGPRX4 in sensory neurons exhibited robust phosphomonoester prodrug-evoked itch. To characterize and confirm this interaction, we further determined the structure of MRGPRX4 in complex with a phosphate-modified drug through single-particle cryo-electron microscopy (cryo-EM) and identified critical amino acid residues responsible for the binding of the phosphate group. Together, these findings explain how phosphorylated drugs can elicit treatment-limiting itch and identify MRGPRX4 as a potential therapeutic target to suppress itch and to guide future drug design. | |||||||||||||||||||||||||||||||||||||||
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構造の表示
| 構造ビューア | 分子: Molmil Jmol/JSmol |
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ダウンロードとリンク
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ダウンロード
| PDBx/mmCIF形式 | 8yrg.cif.gz | 203.7 KB | 表示 | PDBx/mmCIF形式 |
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| PDB形式 | pdb8yrg.ent.gz | 表示 | PDB形式 | |
| PDBx/mmJSON形式 | 8yrg.json.gz | ツリー表示 | PDBx/mmJSON形式 | |
| その他 | その他のダウンロード |
-検証レポート
| アーカイブディレクトリ | https://data.pdbj.org/pub/pdb/validation_reports/yr/8yrg ftp://data.pdbj.org/pub/pdb/validation_reports/yr/8yrg | HTTPS FTP |
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-関連構造データ
| 関連構造データ | ![]() 39542MC M: このデータのモデリングに利用したマップデータ C: 同じ文献を引用 ( |
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| 類似構造データ | 類似検索 - 機能・相同性 F&H 検索 |
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リンク
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集合体
| 登録構造単位 | ![]()
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| 1 |
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要素
-タンパク質 , 2種, 2分子 BR
| #1: タンパク質 | 分子量: 28084.832 Da / 分子数: 1 / 由来タイプ: 組換発現 / 由来: (組換発現) Homo sapiens (ヒト)発現宿主: ![]() |
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| #5: タンパク質 | 分子量: 53396.020 Da / 分子数: 1 / 由来タイプ: 組換発現 / 由来: (組換発現) Homo sapiens (ヒト) / 遺伝子: cybC, MRGPRX4, MRGX4, SNSR5, SNSR6発現宿主: ![]() 参照: UniProt: P0ABE7, UniProt: Q96LA9 |
-Guanine nucleotide-binding protein ... , 2種, 2分子 CD
| #2: タンパク質 | 分子量: 39418.086 Da / 分子数: 1 / 由来タイプ: 組換発現 / 由来: (組換発現) Homo sapiens (ヒト) / 遺伝子: GNB1発現宿主: ![]() 参照: UniProt: P62873 |
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| #3: タンパク質 | 分子量: 7861.143 Da / 分子数: 1 / 由来タイプ: 組換発現 / 由来: (組換発現) Homo sapiens (ヒト) / 遺伝子: GNG2発現宿主: ![]() 参照: UniProt: P59768 |
-抗体 / 非ポリマー , 2種, 2分子 E
| #4: 抗体 | 分子量: 28668.922 Da / 分子数: 1 / 由来タイプ: 組換発現 / 由来: (組換発現) ![]() 発現宿主: ![]() |
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| #6: 化合物 | ChemComp-A1LZU / [ 分子量: 288.277 Da / 分子数: 1 / 由来タイプ: 合成 / 式: C13H21O5P / タイプ: SUBJECT OF INVESTIGATION |
-詳細
| 研究の焦点であるリガンドがあるか | Y |
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| Has protein modification | Y |
-実験情報
-実験
| 実験 | 手法: 電子顕微鏡法 |
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| EM実験 | 試料の集合状態: PARTICLE / 3次元再構成法: 単粒子再構成法 |
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試料調製
| 構成要素 | 名称: fospropofol-bound MRGPRX4-Gq complex / タイプ: COMPLEX / Entity ID: #1-#5 / 由来: RECOMBINANT |
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| 分子量 | 値: 150 kDa/nm / 実験値: NO |
| 由来(天然) | 生物種: Homo sapiens (ヒト) |
| 由来(組換発現) | 生物種: ![]() |
| 緩衝液 | pH: 7.4 |
| 試料 | 包埋: NO / シャドウイング: NO / 染色: NO / 凍結: YES |
| 急速凍結 | 凍結剤: ETHANE-PROPANE / 湿度: 100 % |
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電子顕微鏡撮影
| 実験機器 | ![]() モデル: Talos Arctica / 画像提供: FEI Company |
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| 顕微鏡 | モデル: FEI TALOS ARCTICA |
| 電子銃 | 電子線源: FIELD EMISSION GUN / 加速電圧: 200 kV / 照射モード: FLOOD BEAM |
| 電子レンズ | モード: BRIGHT FIELD / 最大 デフォーカス(公称値): 28000 nm / 最小 デフォーカス(公称値): 200 nm |
| 撮影 | 電子線照射量: 56.5 e/Å2 / フィルム・検出器のモデル: GATAN K3 (6k x 4k) |
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解析
| EMソフトウェア | 名称: PHENIX / カテゴリ: モデル精密化 |
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| CTF補正 | タイプ: PHASE FLIPPING AND AMPLITUDE CORRECTION |
| 3次元再構成 | 解像度: 3.14 Å / 解像度の算出法: FSC 0.143 CUT-OFF / 粒子像の数: 375325 / 対称性のタイプ: POINT |
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万見について




Homo sapiens (ヒト)

米国, 2件
引用
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FIELD EMISSION GUN