+データを開く
-基本情報
登録情報 | データベース: PDB / ID: 8b7q | ||||||
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タイトル | Cryo-EM structure for the mouse LEPR-CRH2:Leptin:LEPR-Ig complex following symmetry expansion in combination with local refinement | ||||||
要素 |
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キーワード | CYTOKINE / leptin / LEP-R / obesity / metabolism / energy balance | ||||||
機能・相同性 | 機能・相同性情報 negative regulation of metabolic process / negative regulation of locomotor rhythm / Synthesis, secretion, and deacylation of Ghrelin / negative regulation of eating behavior / regulation of lipoprotein lipid oxidation / cellular response to L-ascorbic acid / positive regulation of fat cell apoptotic process / negative regulation of glutamine transport / leptin receptor activity / negative regulation of appetite by leptin-mediated signaling pathway ...negative regulation of metabolic process / negative regulation of locomotor rhythm / Synthesis, secretion, and deacylation of Ghrelin / negative regulation of eating behavior / regulation of lipoprotein lipid oxidation / cellular response to L-ascorbic acid / positive regulation of fat cell apoptotic process / negative regulation of glutamine transport / leptin receptor activity / negative regulation of appetite by leptin-mediated signaling pathway / Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) / protein-hormone receptor activity / negative regulation of glucagon secretion / regulation of endothelial cell proliferation / regulation of natural killer cell proliferation / leptin receptor binding / positive regulation of luteinizing hormone secretion / regulation of natural killer cell mediated cytotoxicity / bone growth / regulation of natural killer cell activation / positive regulation of monoatomic ion transport / glycerol biosynthetic process / elastin metabolic process / leptin-mediated signaling pathway / positive regulation of follicle-stimulating hormone secretion / regulation of steroid biosynthetic process / regulation of intestinal cholesterol absorption / regulation of bone remodeling / regulation of brown fat cell differentiation / positive regulation of peroxisome proliferator activated receptor signaling pathway / positive regulation of hepatic stellate cell activation / response to leptin / adult feeding behavior / regulation of nitric-oxide synthase activity / bone mineralization involved in bone maturation / sexual reproduction / regulation of lipid biosynthetic process / regulation of feeding behavior / activation of protein kinase C activity / fatty acid catabolic process / negative regulation of cartilage development / ovulation from ovarian follicle / negative regulation of appetite / positive regulation of developmental growth / leukocyte tethering or rolling / energy reserve metabolic process / bile acid metabolic process / negative regulation of glucose import / prostaglandin secretion / tyrosine phosphorylation of STAT protein / cellular response to leptin stimulus / regulation of protein localization to nucleus / regulation of metabolic process / cardiac muscle hypertrophy / hormone metabolic process / aorta development / negative regulation of lipid storage / cytokine receptor activity / insulin secretion / intestinal absorption / regulation of fat cell differentiation / positive regulation of p38MAPK cascade / peptide hormone receptor binding / negative regulation of vasoconstriction / eating behavior / regulation of gluconeogenesis / glycogen metabolic process / fatty acid beta-oxidation / central nervous system neuron development / regulation of cytokine production involved in inflammatory response / positive regulation of insulin secretion involved in cellular response to glucose stimulus / cytokine binding / peptide hormone binding / regulation of insulin secretion / response to dietary excess / T cell differentiation / positive regulation of TOR signaling / response to vitamin E / glial cell proliferation / regulation of angiogenesis / negative regulation of gluconeogenesis / adipose tissue development / phagocytosis / positive regulation of insulin receptor signaling pathway / cellular response to retinoic acid / positive regulation of T cell proliferation / energy homeostasis / positive regulation of tyrosine phosphorylation of STAT protein / positive regulation of interleukin-12 production / cholesterol metabolic process / negative regulation of autophagy / response to activity / positive regulation of interleukin-8 production / placenta development / gluconeogenesis / female pregnancy / determination of adult lifespan / lipid metabolic process / positive regulation of receptor signaling pathway via JAK-STAT / regulation of protein phosphorylation 類似検索 - 分子機能 | ||||||
生物種 | Mus musculus (ハツカネズミ) | ||||||
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: 4.02 Å | ||||||
データ登録者 | Verstraete, K. / Savvides, S.N. / Verschueren, K.G. / Tsirigotaki, A. | ||||||
資金援助 | ベルギー, 1件
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引用 | ジャーナル: Nat Struct Mol Biol / 年: 2023 タイトル: Mechanism of receptor assembly via the pleiotropic adipokine Leptin. 著者: Alexandra Tsirigotaki / Ann Dansercoer / Koen H G Verschueren / Iva Marković / Christoph Pollmann / Maximillian Hafer / Jan Felix / Catherine Birck / Wouter Van Putte / Dominiek Catteeuw / ...著者: Alexandra Tsirigotaki / Ann Dansercoer / Koen H G Verschueren / Iva Marković / Christoph Pollmann / Maximillian Hafer / Jan Felix / Catherine Birck / Wouter Van Putte / Dominiek Catteeuw / Jan Tavernier / J Fernando Bazan / Jacob Piehler / Savvas N Savvides / Kenneth Verstraete / 要旨: The adipokine Leptin activates its receptor LEP-R in the hypothalamus to regulate body weight and exerts additional pleiotropic functions in immunity, fertility and cancer. However, the structure and ...The adipokine Leptin activates its receptor LEP-R in the hypothalamus to regulate body weight and exerts additional pleiotropic functions in immunity, fertility and cancer. However, the structure and mechanism of Leptin-mediated LEP-R assemblies has remained unclear. Intriguingly, the signaling-competent isoform of LEP-R is only lowly abundant amid several inactive short LEP-R isoforms contributing to a mechanistic conundrum. Here we show by X-ray crystallography and cryo-EM that, in contrast to long-standing paradigms, Leptin induces type I cytokine receptor assemblies featuring 3:3 stoichiometry and demonstrate such Leptin-induced trimerization of LEP-R on living cells via single-molecule microscopy. In mediating these assemblies, Leptin undergoes drastic restructuring that activates its site III for binding to the Ig domain of an adjacent LEP-R. These interactions are abolished by mutations linked to obesity. Collectively, our study provides the structural and mechanistic framework for how evolutionarily conserved Leptin:LEP-R assemblies with 3:3 stoichiometry can engage distinct LEP-R isoforms to achieve signaling. | ||||||
履歴 |
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-構造の表示
構造ビューア | 分子: MolmilJmol/JSmol |
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-ダウンロードとリンク
-ダウンロード
PDBx/mmCIF形式 | 8b7q.cif.gz | 148.4 KB | 表示 | PDBx/mmCIF形式 |
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PDB形式 | pdb8b7q.ent.gz | 93.2 KB | 表示 | PDB形式 |
PDBx/mmJSON形式 | 8b7q.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
文書・要旨 | 8b7q_validation.pdf.gz | 1.4 MB | 表示 | wwPDB検証レポート |
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文書・詳細版 | 8b7q_full_validation.pdf.gz | 1.4 MB | 表示 | |
XML形式データ | 8b7q_validation.xml.gz | 36.6 KB | 表示 | |
CIF形式データ | 8b7q_validation.cif.gz | 50.5 KB | 表示 | |
アーカイブディレクトリ | https://data.pdbj.org/pub/pdb/validation_reports/b7/8b7q ftp://data.pdbj.org/pub/pdb/validation_reports/b7/8b7q | HTTPS FTP |
-関連構造データ
関連構造データ | 15899MC 7z3pC 7z3qC 7z3rC 8av2C 8avbC 8avcC 8avdC 8aveC 8avfC 8avoC C: 同じ文献を引用 (文献) M: このデータのモデリングに利用したマップデータ |
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類似構造データ | 類似検索 - 機能・相同性F&H 検索 |
-リンク
-集合体
登録構造単位 |
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1 |
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-要素
#1: タンパク質 | 分子量: 18873.283 Da / 分子数: 1 / 由来タイプ: 組換発現 詳細: Mouse leptin was produced with an N-terminal His-tag and refolded from inclusion bodies produced in E. coli 由来: (組換発現) Mus musculus (ハツカネズミ) / 遺伝子: Lep, Ob / プラスミド: pET15b / 詳細 (発現宿主): pET15b-His-TEV-mLeptin / 発現宿主: Escherichia coli BL21(DE3) (大腸菌) / 参照: UniProt: P41160 | ||||
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#2: タンパク質 | 分子量: 97479.391 Da / 分子数: 2 / 由来タイプ: 組換発現 詳細: The mLEP-R ectodomain was C-terminally fused to a trimeric GCN4 isoleucine zipper tag and secreted from HEK93 FreeStyle cells and complexed with refolded mouse leptin produced in E.coli. 由来: (組換発現) Mus musculus (ハツカネズミ) / 遺伝子: Lepr, Db, Obr / プラスミド: pTwist / 細胞株 (発現宿主): HEK293 / 発現宿主: Homo sapiens (ヒト) / Variant (発現宿主): FreeStyle / 参照: UniProt: P48356 #3: 糖 | ChemComp-NAG / | 研究の焦点であるリガンドがあるか | 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 |
-試料調製
構成要素 | 名称: Mouse leptin in complex with a trimerized form of the mouse Lep-R extracellular region タイプ: COMPLEX 詳細: The mLEP-R ectodomain was C-terminally fused to a trimeric GCN4 isoleucine zipper tag and secreted from HEK93 FreeStyle cells and complexed with refolded mouse leptin produced in E.coli. Entity ID: #1-#2 / 由来: RECOMBINANT | |||||||||||||||
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分子量 | 値: 0.444 MDa / 実験値: YES | |||||||||||||||
由来(天然) | 生物種: Mus musculus (ハツカネズミ) | |||||||||||||||
由来(組換発現) | 生物種: Homo sapiens (ヒト) | |||||||||||||||
緩衝液 | pH: 7.4 / 詳細: 20 mM HEPES, 150 mM NaCl, pH 7.4 | |||||||||||||||
緩衝液成分 |
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試料 | 濃度: 0.3 mg/ml / 包埋: NO / シャドウイング: NO / 染色: NO / 凍結: YES / 詳細: This sample was monodisperse. | |||||||||||||||
試料支持 | グリッドの材料: COPPER / グリッドのサイズ: 300 divisions/in. / グリッドのタイプ: C-flat-1.2/1.3 | |||||||||||||||
急速凍結 | 装置: LEICA EM GP / 凍結剤: ETHANE / 湿度: 99 % / 凍結前の試料温度: 295 K |
-電子顕微鏡撮影
実験機器 | モデル: Titan Krios / 画像提供: FEI Company |
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顕微鏡 | モデル: TFS KRIOS |
電子銃 | 電子線源: FIELD EMISSION GUN / 加速電圧: 300 kV / 照射モード: FLOOD BEAM |
電子レンズ | モード: OTHER / 倍率(公称値): 105000 X / 最大 デフォーカス(公称値): 2500 nm / 最小 デフォーカス(公称値): 1200 nm / Cs: 2.7 mm |
撮影 | 電子線照射量: 45 e/Å2 フィルム・検出器のモデル: GATAN K3 BIOQUANTUM (6k x 4k) 撮影したグリッド数: 1 / 実像数: 13230 |
-解析
ソフトウェア |
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EMソフトウェア |
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CTF補正 | タイプ: PHASE FLIPPING AND AMPLITUDE CORRECTION | |||||||||||||||||||||||||||||||||||
粒子像の選択 | 選択した粒子像数: 141157 | |||||||||||||||||||||||||||||||||||
対称性 | 点対称性: C1 (非対称) | |||||||||||||||||||||||||||||||||||
3次元再構成 | 解像度: 4.02 Å / 解像度の算出法: FSC 0.143 CUT-OFF / 粒子像の数: 163914 詳細: To address the breakage of symmetry in the ring-like core region of the complex and possibly revolve the mLEP-RCRH2:mLeptin:mLEP-RCRH1-IgCRH2 subcomplex at higher resolution, the pseudo-C3 ...詳細: To address the breakage of symmetry in the ring-like core region of the complex and possibly revolve the mLEP-RCRH2:mLeptin:mLEP-RCRH1-IgCRH2 subcomplex at higher resolution, the pseudo-C3 symmetric volume following consenus refinement was aligned to the pseudo-C3 symmetry axis via the Volume Alignment Tool job in cryoSPARC. The associated particle set was re-extracted without binning and symmetry expanded around the C3 axis resulting in 163,914 particles. Using the molmap function in Chimera, a volume blurred to 25 Angstrom around one mLEP-RCRH2:mLeptin:mLEP-RCRH1-IgCRH2 subcomplex was generated, and transformed into a mask with the Volume Tools job in cryoSPARC. Local refinement was performed by limiting the rotation and shift search extent around the original consensus refinement. The center of mass of the mask was used as a fulcrum point. This approach resulted in a cryo-EM map with an FSC0.143 resolution of 4.02 Angstrom in which the crystallographic model for the mLEP-RCRH2:mLeptin:mLEP-R_IgCRH2' complex was fitted using Chimera and real-space refined in Phenix using reference restraints to the starting model. 対称性のタイプ: POINT | |||||||||||||||||||||||||||||||||||
原子モデル構築 | プロトコル: FLEXIBLE FIT / 空間: REAL 詳細: The crystallographic model for the mLEP-RCRH2:mLeptin:mLEP-R_IgCRH2' complex (pdb 7z3r) was fitted in the cryo-EM map using Chimera and real-space refined in Phenix using reference restraints ...詳細: The crystallographic model for the mLEP-RCRH2:mLeptin:mLEP-R_IgCRH2' complex (pdb 7z3r) was fitted in the cryo-EM map using Chimera and real-space refined in Phenix using reference restraints to the starting model. | |||||||||||||||||||||||||||||||||||
精密化 | 交差検証法: NONE 立体化学のターゲット値: GeoStd + Monomer Library + CDL v1.2 | |||||||||||||||||||||||||||||||||||
原子変位パラメータ | Biso mean: 101.59 Å2 | |||||||||||||||||||||||||||||||||||
拘束条件 |
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