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- EMDB-26183: Cryo-EM Structure of insulin receptor-related receptor (IRR) in a... -

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Basic information

Entry
Database: EMDB / ID: EMD-26183
TitleCryo-EM Structure of insulin receptor-related receptor (IRR) in apo-state captured at pH 7. The 3D refinement was applied with C2 symmetry
Map dataCryo-EM Structure of insulin receptor-related receptor (IRR) in apo-state captured at pH 7. The 3D refinement was applied with C2 symmetry.
Sample
  • Complex: Insulin receptor-related receptor (IRR) in apo-state captured at pH 7
    • Protein or peptide: Insulin receptor-related protein
KeywordsReceptor tyrosine kinase / insulin receptor family / SIGNALING PROTEIN
Function / homology
Function and homology information


cellular response to alkaline pH / male sex determination / insulin receptor complex / insulin receptor activity / insulin receptor substrate binding / phosphatidylinositol 3-kinase binding / transmembrane receptor protein tyrosine kinase activity / receptor protein-tyrosine kinase / cell surface receptor protein tyrosine kinase signaling pathway / actin cytoskeleton organization ...cellular response to alkaline pH / male sex determination / insulin receptor complex / insulin receptor activity / insulin receptor substrate binding / phosphatidylinositol 3-kinase binding / transmembrane receptor protein tyrosine kinase activity / receptor protein-tyrosine kinase / cell surface receptor protein tyrosine kinase signaling pathway / actin cytoskeleton organization / protein autophosphorylation / receptor complex / axon / ATP binding / plasma membrane
Similarity search - Function
Tyrosine-protein kinase, insulin-like receptor / Tyrosine-protein kinase, receptor class II, conserved site / Receptor tyrosine kinase class II signature. / Receptor L-domain / Furin-like cysteine-rich domain / Receptor L-domain superfamily / Furin-like cysteine rich region / Receptor L domain / Furin-like repeat / Furin-like repeats ...Tyrosine-protein kinase, insulin-like receptor / Tyrosine-protein kinase, receptor class II, conserved site / Receptor tyrosine kinase class II signature. / Receptor L-domain / Furin-like cysteine-rich domain / Receptor L-domain superfamily / Furin-like cysteine rich region / Receptor L domain / Furin-like repeat / Furin-like repeats / Growth factor receptor cysteine-rich domain superfamily / Fibronectin type 3 domain / Fibronectin type-III domain profile. / Fibronectin type III / Fibronectin type III superfamily / Tyrosine-protein kinase, catalytic domain / Tyrosine kinase, catalytic domain / Tyrosine protein kinases specific active-site signature. / Tyrosine-protein kinase, active site / Protein tyrosine and serine/threonine kinase / Serine-threonine/tyrosine-protein kinase, catalytic domain / Protein kinase, ATP binding site / Protein kinases ATP-binding region signature. / Immunoglobulin-like fold / Protein kinase domain profile. / Protein kinase domain / Protein kinase-like domain superfamily
Similarity search - Domain/homology
Insulin receptor-related protein
Similarity search - Component
Biological speciesHomo sapiens (human)
Methodsingle particle reconstruction / cryo EM / Resolution: 3.5 Å
AuthorsWang LW / Hall C / Li J / Choi E / Bai XC
Funding support United States, 2 items
OrganizationGrant numberCountry
National Institutes of Health/National Institute of General Medical Sciences (NIH/NIGMS)R01GM136976 United States
National Institutes of Health/National Institute of General Medical Sciences (NIH/NIGMS)R35GM142937 United States
CitationJournal: Nat Struct Mol Biol / Year: 2023
Title: Structural basis of the alkaline pH-dependent activation of insulin receptor-related receptor.
Authors: Liwei Wang / Catherine Hall / Jie Li / Eunhee Choi / Xiao-Chen Bai /
Abstract: The insulin receptor (IR) family is a subfamily of receptor tyrosine kinases that controls metabolic homeostasis and cell growth. Distinct from IR and insulin-like growth factor 1 receptor, whose ...The insulin receptor (IR) family is a subfamily of receptor tyrosine kinases that controls metabolic homeostasis and cell growth. Distinct from IR and insulin-like growth factor 1 receptor, whose activation requires ligand binding, insulin receptor-related receptor (IRR)-the third member of the IR family-is activated by alkaline pH. However, the molecular mechanism underlying alkaline pH-induced IRR activation remains unclear. Here, we present cryo-EM structures of human IRR in both neutral pH inactive and alkaline pH active states. Combined with mutagenesis and cellular assays, we show that, upon pH increase, electrostatic repulsion of the pH-sensitive motifs of IRR disrupts its autoinhibited state and promotes a scissor-like rotation between two protomers, leading to a T-shaped active conformation. Together, our study reveals an unprecedented alkaline pH-dependent activation mechanism of IRR, opening up opportunities to understand the structure-function relationship of this important receptor.
History
DepositionFeb 13, 2022-
Header (metadata) releaseFeb 15, 2023-
Map releaseFeb 15, 2023-
UpdateMay 31, 2023-
Current statusMay 31, 2023Processing site: RCSB / Status: Released

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Structure visualization

Supplemental images

emd_26183.png

Downloads & links

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Map

FileDownload / File: emd_26183.map.gz / Format: CCP4 / Size: 52.7 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES)
AnnotationCryo-EM Structure of insulin receptor-related receptor (IRR) in apo-state captured at pH 7. The 3D refinement was applied with C2 symmetry.
Voxel sizeX=Y=Z: 1.08 Å
Density
Contour LevelBy AUTHOR: 0.03
Minimum - Maximum-0.13867101 - 0.2037988
Average (Standard dev.)0.00006369555 (±0.0065029114)
SymmetrySpace group: 1
Details

EMDB XML:

Map geometry
Axis orderXYZ
Origin000
Dimensions240240240
Spacing240240240
CellA=B=C: 259.2 Å
α=β=γ: 90.0 °

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Supplemental data

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Sample components

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Entire : Insulin receptor-related receptor (IRR) in apo-state captured at pH 7

EntireName: Insulin receptor-related receptor (IRR) in apo-state captured at pH 7
Components
  • Complex: Insulin receptor-related receptor (IRR) in apo-state captured at pH 7
    • Protein or peptide: Insulin receptor-related protein

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Supramolecule #1: Insulin receptor-related receptor (IRR) in apo-state captured at pH 7

SupramoleculeName: Insulin receptor-related receptor (IRR) in apo-state captured at pH 7
type: complex / ID: 1 / Parent: 0 / Macromolecule list: all
Source (natural)Organism: Homo sapiens (human)
Molecular weightTheoretical: 140 KDa

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Macromolecule #1: Insulin receptor-related protein

MacromoleculeName: Insulin receptor-related protein / type: protein_or_peptide / ID: 1 / Number of copies: 2 / Enantiomer: LEVO / EC number: receptor protein-tyrosine kinase
Source (natural)Organism: Homo sapiens (human)
Molecular weightTheoretical: 143.879547 KDa
Recombinant expressionOrganism: Homo sapiens (human)
SequenceString: MAVPSLWPWG ACLPVIFLSL GFGLDTVEVC PSLDIRSEVA ELRQLENCSV VEGHLQILLM FTATGEDFRG LSFPRLTQVT DYLLLFRVY GLESLRDLFP NLAVIRGTRL FLGYALVIFE MPHLRDVALP ALGAVLRGAV RVEKNQELCH LSTIDWGLLQ P APGANHIV ...String:
MAVPSLWPWG ACLPVIFLSL GFGLDTVEVC PSLDIRSEVA ELRQLENCSV VEGHLQILLM FTATGEDFRG LSFPRLTQVT DYLLLFRVY GLESLRDLFP NLAVIRGTRL FLGYALVIFE MPHLRDVALP ALGAVLRGAV RVEKNQELCH LSTIDWGLLQ P APGANHIV GNKLGEECAD VCPGVLGAAG EPCAKTTFSG HTDYRCWTSS HCQRVCPCPH GMACTARGEC CHTECLGGCS QP EDPRACV ACRHLYFQGA CLWACPPGTY QYESWRCVTA ERCASLHSVP GRASTFGIHQ GSCLAQCPSG FTRNSSSIFC HKC EGLCPK ECKVGTKTID SIQAAQDLVG CTHVEGSLIL NLRQGYNLEP QLQHSLGLVE TITGFLKIKH SFALVSLGFF KNLK LIRGD AMVDGNYTLY VLDNQNLQQL GSWVAAGLTI PVGKIYFAFN PRLCLEHIYR LEEVTGTRGR QNKAEINPRT NGDRA ACQT RTLRFVSNVT EADRILLRWE RYEPLEARDL LSFIVYYKES PFQNATEHVG PDACGTQSWN LLDVELPLSR TQEPGV TLA SLKPWTQYAV FVRAITLTTE EDSPHQGAQS PIVYLRTLPA APTVPQDVIS TSNSSSHLLV RWKPPTQRNG NLTYYLV LW QRLAEDGDLY LNDYCHRGLR LPTSNNDPRF DGEDGDPEAE MESDCCPCQH PPPGQVLPPL EAQEASFQKK FENFLHNA I TIPISPWKVT SINKSPQRDS GRHRRAAGPL RLGGNSSDFE IQEDKVPRER AVLSGLRHFT EYRIDIHACN HAAHTVGCS AATFVFARTM PHREADGIPG KVAWEASSKN SVLLRWLEPP DPNGLILKYE IKYRRLGEEA TVLCVSRLRY AKFGGVHLAL LPPGNYSAR VRATSLAGNG SWTDSVAFYI LGPEEEDAGG LHVLLTATPV GLTLLIVLAA LGFFYGKKRN RTLYASVNPE Y FSASDMYV PDEWEVPREQ ISIIRELGQG SFGMVYEGLA RGLEAGEEST PVALKTVNEL ASPRECIEFL KEASVMKAFK CH HVVRLLG VVSQGQPTLV IMELMTRGDL KSHLRSLRPE AENNPGLPQP ALGEMIQMAG EIADGMAYLA ANKFVHRDLA ARN CMVSQD FTVKIGDFGM TRDVYETDYY RKGGKGLLPV RWMAPESLKD GIFTTHSDVW SFGVVLWEIV TLAEQPYQGL SNEQ VLKFV MDGGVLEELE GCPLQLQELM SRCWQPNPRL RPSFTHILDS IQEELRPSFR LLSFYYSPEC RGARGSLPTT DAEPD SSPT PRDCSPQNGG PGH

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Experimental details

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Structure determination

Methodcryo EM
Processingsingle particle reconstruction
Aggregation stateparticle

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Sample preparation

Concentration6 mg/mL
BufferpH: 7
VitrificationCryogen name: ETHANE / Chamber humidity: 100 %

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Electron microscopy

MicroscopeFEI TITAN KRIOS
Electron beamAcceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN
Electron opticsIllumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELDBright-field microscopy / Nominal defocus max: 2.6 µm / Nominal defocus min: 1.6 µm
Specialist opticsEnergy filter - Name: GIF Bioquantum / Energy filter - Slit width: 20 eV
Sample stageSpecimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN
Image recordingFilm or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Average electron dose: 60.0 e/Å2
Experimental equipment
Model: Titan Krios / Image courtesy: FEI Company

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Image processing

Particle selectionNumber selected: 4993810
Startup modelType of model: OTHER
Initial angle assignmentType: PROJECTION MATCHING / Software - Name: RELION
Final 3D classificationSoftware - Name: RELION
Final angle assignmentType: PROJECTION MATCHING / Software - Name: RELION
Final reconstructionApplied symmetry - Point group: C2 (2 fold cyclic) / Resolution.type: BY AUTHOR / Resolution: 3.5 Å / Resolution method: FSC 0.143 CUT-OFF / Software - Name: RELION / Number images used: 129384

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Atomic model buiding 1

RefinementSpace: REAL / Protocol: AB INITIO MODEL
Output model

PDB-7tyk:
Cryo-EM Structure of insulin receptor-related receptor (IRR) in apo-state captured at pH 7. The 3D refinement was applied with C2 symmetry

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