SASDXH4

Mouse complex murine Immunoglobulin E (IgE) antibody with profilin (without HisTAG)

Data type: SASBDB experimental data Status: Published Curve type: SEC-SAS Last updated: 2025-09-17T10:13:06.720266+02:00

The molecular weight estimate is an approximation; the actual molecular weight can vary depending on the specific glycosylation patterns and modifications of the IgE molecule. In this way, the estimated MW for the complex (including the theProfilin) is approximately 240 kDa. For the model for IgE structure, we developed a hybrid model inspired by Jansen et al., 2020. This model incorporates two Fab regions (allergen excluded) from the crystallographic structure (PDB entry 7SBD), combined with an extended human Fc fragment (CH2-CH3-CH4) from PDB entry 4J4P. The hybrid model was manually fitted into a low-resolution SAXS envelope obtained by using the DAMMIF, DAMAVER, and DAMMIN programs (SASBDB entry SASDVG9). This model for IgE was used to generate the IgE complex with the allergen (Profilin) using crystallographic structure (PDB entry 7SBD) fitting a low-resolution SAXS envelope obtained by DAMMIN program. Further refinement of the hybrid model was conducted through Normal Mode Analysis (NMA) using the SREFLEX program based on experimental SAXS data.

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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · Mouse complex murine Immunoglobulin E (IgE) antibody with profilin (without HisTAG)

Concentration— – 6.0 Buffer / pH20 mM Tris, 50 mM NaCl / 8.4
Experimental temperature20.0 Facility / beamlinePETRA III / EMBL P12
Wavelength0.124 nmExposure1.0 s × 3000

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
Murine Immunoglobulin E (IgE) antibodies
View sequence
EVQLVESGGGLVQPKGSLKLSCAASGFTFNTYAMNWVRQAPGKGLEWVARIRTKTNNYVTYYADSVKDRFTISRDDSQSMLYLQMNNLKTEDTAMYYCVRHVGDYWGQGTSVTVSSASIRNPQLYPLKPCKSMTLGCLVKDYFPGPVTVTWYSDSLNMSTVNFPALGSELKVTTSQVTSWGKSAKNFTCHVTHPPSFNESRTILVRPVNITEPTLELLHSSCDPNAFHSTIQLYCFIYGHILNDVSVSWLMDDREITDTLAQTVLIKEEGKLASTCSKLNITEQQWMSESTFTCKVTSQGVDYLAHTRRCPDHEPRGVITYLIPPSPLDLYQNGAPKLTCLVVDLESEKNVNVTWNQEKKTSVSASQWYTKHHNNATTSITSILPVVAKDWIEGYGYQCIVDHPDFPKPIVRSITKTPGQRSAPEVYVFPPPEEESEDKRTLTCLIQNFFPEDISVQWLGDGKLISNSQHSTTTPLKSNGSNQGFFIFSRLEVAKTLWTQRKQFTCQVIHEALQKPRKLEKTISTSDIQMTQSPASLSASVGETVTITCRASGNIHNYLAWFQQKQGKSPQLLVYNAKTLADGVPSRFSGSGSGTQYSLKINSLQPEDFGSYYCQHFWSTPYTFGGGTKLEIKRADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPKDINVKWKIDGSERQNGVLNSWTDQDSKDSTYSMSSTLTLTKDEYERHNSYTCEATHKTSTSPIVKSFNRNEEVQLVESGGGLVQPKGSLKLSCAASGFTFNTYAMNWVRQAPGKGLEWVARIRTKTNNYVTYYADSVKDRFTISRDDSQSMLYLQMNNLKTEDTAMYYCVRHVGDYWGQGTSVTVSSASIRNPQLYPLKPCKSMTLGCLVKDYFPGPVTVTWYSDSLNMSTVNFPALGSELKVTTSQVTSWGKSAKNFTCHVTHPPSFNESRTILVRPVNITEPTLELLHSSCDPNAFHSTIQLYCFIYGHILNDVSVSWLMDDREITDTLAQTVLIKEEGKLASTCSKLNITEQQWMSESTFTCKVTSQGVDYLAHTRRCPDHEPRGVITYLIPPSPLDLYQNGAPKLTCLVVDLESEKNVNVTWNQEKKTSVSASQWYTKHHNNATTSITSILPVVAKDWIEGYGYQCIVDHPDFPKPIVRSITKTPGQRSAPEVYVFPPPEEESEDKRTLTCLIQNFFPEDISVQWLGDGKLISNSQHSTTTPLKSNGSNQGFFIFSRLEVAKTLWTQRKQFTCQVIHEALQKPRKLEKTISTSLDIQMTQSPASLSASVGETVTITCRASGNIHNYLAWFQQKQGKSPQLLVYNAKTLADGVPSRFSGSGSGTQYSLKINSLQPEDFGSYYCQHFWSTPYTFGGGTKLEIKRADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPKDINVKWKIDGSERQNGVLNSWTDQDSKDSTYSMSSTLTLTKDEYERHNSYTCEATHKTSTSPIVKSFNRNE
proteinMus musculus——–—monomerMolecule count 1165.383 kDa
Profilin-2
View sequence
MGSSHHHHHHSSGLVPRGSHMASMTGGQQMGRGSDDDDKMSWQAYVDDHLMCEIEGNHLSAAAIIGQDGSVWAQSANFPQFKSEEITGIMSDFHEPGTLAPTGLYIGGTKYMVIQGEPGAVIRGKKGPGGVTVKKTNQALIIGIYDEPMTPGQCNMIVERLGDYLIDQGY
proteinHevea brasiliensisQ9STB61–131monomerMolecule count 118.283 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
12591[3]0.02255827–7.269159 1/nmHas uncertainty columnMissing 0613sasbdb/entries/h4/sasdxh4/source/SASDXH4.dat
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2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)19.94—nm
i0Guinier0.0336798—1/cm
i0P(r)0.03409—1/cm
mwExperimental249.0—kDa
mwPorod260.0—kDa
porod_volumePorod450.0—nm³
rgGuinier5.7370.026nm
rgP(r)5.937—nm

These values are reported by SASBDB; SAXSdb did not recalculate them from the experimental curve.

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3. Source Fits and Models Source Fits & Models

Fit 1 · SREFLEX 4.0

χ²: 1.073CorMap p: 0.1937Unit: 1/A
ModelName / TypeSoftwareSymmetryModel MWPDB DeclarationSource file
1—atomicSREFLEX —182.8—Model Image
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4. Source File Index Source Files

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5. Experiment Description and Publication Experiment & Publication

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6. Complete Source Record Complete Source Record

The following content comes directly from the SASBDB entry. Missing values are shown as “—”; SAXSdb does not infer undeclared units.

Open the original SASBDB entry

Buffer and Sample Properties

Buffer name20 mM Tris, 50 mM NaClBuffer concentration—
pH8.4Additives—
Buffer description—
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2025-04-11Storage / measurement temperature4.0 / 20.0
Exposure time1.0Frames3000
Wavelength0.124Sample-to-detector distance3.0
SourceX-ray synchrotronDetectorPilatus 6M
Facility / beamlinePETRA III / EMBL P12 · DESY; Hamburg, Germany
q range0.023 – 7.269Sample volume / flow rate50.0 / 0.75

Original SASBDB Plots

Experimental I(q)
Experimental I(q)
Experimental I(q), log-log
Experimental I(q), log-log
Guinier plot
Guinier plot
Kratky plot
Kratky plot
P(r) plot
P(r) plot

Downloadable Files

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All source fields (unfiltered)

Every source field is expanded here, including empty values, list members and fields already shown above.

summary.json:196 field values
Field pathRaw value
codeSASDXH4
statusPublished
type_of_curveSEC-SAS
angular_unit1/nm
project.titleAllergen-induced structural rearrangements in IgE: insights from SAXS and molecular dynamics.
project.publication.titleAllergen-induced structural rearrangements in IgE: insights from SAXS and molecular dynamics.
project.publication.author_listGómez-Velasco H, García-Ramírez B, Siliqi D, Graewert MA, Quintero-Martinez A, Ortega E, Rodríguez-Romero A
project.publication.journalInt J Biol Macromol
project.publication.doi10.1016/j.ijbiomac.2025.147658
project.publication.pmid40953619
project.publication.published_date2025 Sep 13
project.statusreleased
project.submitted_date2025-05-07
project.released_date2025-09-17
pddf_datahttps://www.sasbdb.org/media/p_of_R_files/SASDXH4.out
intensities_datahttps://www.sasbdb.org/media/intensities_files/SASDXH4.dat
intensities_log_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDXH4_dat_img.png
intensities_kratky_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDXH4_kratky_img.png
pddf_plothttps://www.sasbdb.org/media/p_of_R_files/pofr_images/SASDXH4_pofr_img.png
intensities_guinier_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDXH4_guinier_img.png
sascif_datahttps://www.sasbdb.org/media/sascif/sascif_files/SASDXH4.sascif
experiment.instrument.detector.typenull
experiment.instrument.detector.namePilatus 6M
experiment.instrument.detector.resolutionnull
experiment.instrument.namePETRA III
experiment.instrument.cityDESY; Hamburg
experiment.instrument.countryGermany
experiment.instrument.beamline_nameEMBL P12
experiment.instrument.beam_geometrynull
experiment.instrument.type_of_sourceX-ray synchrotron
experiment.instrument.point_sourcenull
experiment.instrument.line_collimationnull
experiment.instrument.sample_path_lengthnull
experiment.instrument.line_collimation_slitlengthnull
experiment.instrument.line_collimation_integrationwidthnull
experiment.instrument.xray_energynull
experiment.instrument.beam_profile_ahnull
experiment.instrument.beam_profile_alnull
experiment.sample.molecule[0].long_nameMurine Immunoglobulin E (IgE) antibodies
experiment.sample.molecule[0].short_nameIgE
experiment.sample.molecule[0].sequenceEVQLVESGGGLVQPKGSLKLSCAASGFTFNTYAMNWVRQAPGKGLEWVARIRTKTNNYVTYYADSVKDRFTISRDDSQSM LYLQMNNLKTEDTAMYYCVRHVGDYWGQGTSVTVSSASIRNPQLYPLKPCKSMTLGCLVKDYFPGPVTVTWYSDSLNMST VNFPALGSELKVTTSQVTSWGKSAKNFTCHVTHPPSFNESRTILVRPVNITEPTLELLHSSCDPNAFHSTIQLYCFIYGH ILNDVSVSWLMDDREITDTLAQTVLIKEEGKLASTCSKLNITEQQWMSESTFTCKVTSQGVDYLAHTRRCPDHEPRGVIT YLIPPSPLDLYQNGAPKLTCLVVDLESEKNVNVTWNQEKKTSVSASQWYTKHHNNATTSITSILPVVAKDWIEGYGYQCI VDHPDFPKPIVRSITKTPGQRSAPEVYVFPPPEEESEDKRTLTCLIQNFFPEDISVQWLGDGKLISNSQHSTTTPLKSNG SNQGFFIFSRLEVAKTLWTQRKQFTCQVIHEALQKPRKLEKTISTS DIQMTQSPASLSASVGETVTITCRASGNIHNYLAWFQQKQGKSPQLLVYNAKTLADGVPSRFSGSGSGTQYSLKINSLQP EDFGSYYCQHFWSTPYTFGGGTKLEIKRADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPKDINVKWKIDGSERQNGVL NSWTDQDSKDSTYSMSSTLTLTKDEYERHNSYTCEATHKTSTSPIVKSFNRNE EVQLVESGGGLVQPKGSLKLSCAASGFTFNTYAMNWVRQAPGKGLEWVARIRTKTNNYVTYYADSVKDRFTISRDDSQSM LYLQMNNLKTEDTAMYYCVRHVGDYWGQGTSVTVSSASIRNPQLYPLKPCKSMTLGCLVKDYFPGPVTVTWYSDSLNMST VNFPALGSELKVTTSQVTSWGKSAKNFTCHVTHPPSFNESRTILVRPVNITEPTLELLHSSCDPNAFHSTIQLYCFIYGH ILNDVSVSWLMDDREITDTLAQTVLIKEEGKLASTCSKLNITEQQWMSESTFTCKVTSQGVDYLAHTRRCPDHEPRGVIT YLIPPSPLDLYQNGAPKLTCLVVDLESEKNVNVTWNQEKKTSVSASQWYTKHHNNATTSITSILPVVAKDWIEGYGYQCI VDHPDFPKPIVRSITKTPGQRSAPEVYVFPPPEEESEDKRTLTCLIQNFFPEDISVQWLGDGKLISNSQHSTTTPLKSNG SNQGFFIFSRLEVAKTLWTQRKQFTCQVIHEALQKPRKLEKTISTSL DIQMTQSPASLSASVGETVTITCRASGNIHNYLAWFQQKQGKSPQLLVYNAKTLADGVPSRFSGSGSGTQYSLKINSLQP EDFGSYYCQHFWSTPYTFGGGTKLEIKRADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPKDINVKWKIDGSERQNGVL NSWTDQDSKDSTYSMSSTLTLTKDEYERHNSYTCEATHKTSTSPIVKSFNRNE
experiment.sample.molecule[0].organismMus musculus
experiment.sample.molecule[0].uniprot_codenull
experiment.sample.molecule[0].uniprot_range_firstnull
experiment.sample.molecule[0].uniprot_range_lastnull
experiment.sample.molecule[0].oligomerizationmonomer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequence
experiment.sample.molecule[0].mw165.383
experiment.sample.molecule[0].total_mw165.383
experiment.sample.molecule[0].number_molecules1
experiment.sample.molecule[0].complex_stateFalse
experiment.sample.molecule[0].deuterationnull
experiment.sample.molecule[0].molecule_sourcebiological
experiment.sample.molecule[0].molecule_descriptionThe molecular weight of a murine IgE, considering glycosylations, is approximately 190-198 kDa (protein 180 kDa + 10-18 kDa glycosylation). This is a rough estimate; the actual molecular weight can vary depending on the specific glycosylation patterns and modifications of the IgE molecule.
experiment.sample.molecule[1].long_nameProfilin-2
experiment.sample.molecule[1].short_namePRF
experiment.sample.molecule[1].sequenceMGSSHHHHHHSSGLVPRGSHMASMTGGQQMGRGSDDDDKMSWQAYVDDHLMCEIEGNHLSAAAIIGQDGSVWAQSANFPQFKSEEITGIMSDFHEPGTLAPTGLYIGGTKYMVIQGEPGAVIRGKKGPGGVTVKKTNQALIIGIYDEPMTPGQCNMIVERLGDYLIDQGY
experiment.sample.molecule[1].organismHevea brasiliensis
experiment.sample.molecule[1].uniprot_codeQ9STB6
experiment.sample.molecule[1].uniprot_range_first1
experiment.sample.molecule[1].uniprot_range_last131
experiment.sample.molecule[1].oligomerizationmonomer
experiment.sample.molecule[1].molecular_typeprotein
experiment.sample.molecule[1].uniprot_sequenceMSWQAYVDDHLMCEIEGNHLSAAAIIGQDGSVWAQSANFPQFKSEEITGIMSDFHEPGTL APTGLYIGGTKYMVIQGEPGAVIRGKKGPGGVTVKKTNQALIIGIYDEPMTPGQCNMIVE RLGDYLIDQGY
experiment.sample.molecule[1].mw18.283
experiment.sample.molecule[1].total_mw18.283
experiment.sample.molecule[1].number_molecules1
experiment.sample.molecule[1].complex_stateFalse
experiment.sample.molecule[1].deuterationnull
experiment.sample.molecule[1].molecule_sourcebiological
experiment.sample.molecule[1].molecule_descriptionAllergen Hev b 8 protein (profilin). The protein construct contains an additional 39 non-native amino acids at the N-terminus (MGSSHHHHHHSSGLVPRGSHMASMTGGQQMGRGSDDDDK).
experiment.sample.buffer.name20 mM Tris, 50 mM NaCl
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentnull
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph8.4
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameMouse complex murine Immunoglobulin E (IgE) antibody with profilin (without HisTAG)
experiment.sample.ext_coefficientnull
experiment.sample.contrastnull
experiment.sample.specific_volnull
experiment.sample.dry_volnull
experiment.sample.absorbptionnull
experiment.sample.deuterationnull
experiment.sample.mixturenull
experiment.contributor[0].affiliation[0].short_namenull
experiment.contributor[0].affiliation[0].addressBari, Italy
experiment.contributor[0].affiliation[0].full_nameCNR - Institute of Crystallography, Bari, Italy
experiment.contributor[0].affiliation[0].webpagehttp://www.ba.ic.cnr.it
experiment.contributor[0].contributor_nameDritan
experiment.contributor[0].contributor_surnameSiliqi
experiment.contributor[0].orcidhttps://orcid.org/0000-0003-1415-8725
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2025-04-11
experiment.storage_temperature4.0
experiment.cell_temperature20.0
experiment.exposure_time1.0
experiment.number_of_frames3000
experiment.wavelength0.124
experiment.sample_detector_distance3.0
experiment.concentration_minnull
experiment.concentration_max6.0
experiment.sample_volume50.0
experiment.flow_rate0.75
experiment.s_min0.023
experiment.s_max7.269
experiment.total_exposure_timenull
experiment.seccolumn1
fits[0].models[0].model_plothttps://www.sasbdb.org/media/pdb_file/images/SASDXH4_fit1_model1_img.png
fits[0].models[0].softwareSREFLEX
fits[0].models[0].pdb_link[]
fits[0].models[0].model_titlenull
fits[0].models[0].type_of_modelatomic
fits[0].models[0].software_versionnull
fits[0].models[0].model_datahttps://www.sasbdb.org/media/pdb_file/SASDXH4_fit1_model1.pdb
fits[0].models[0].model_mw182.8
fits[0].models[0].bead_radiusnull
fits[0].models[0].lognull
fits[0].models[0].symmetrynull
fits[0].models[0].commentnull
fits[0].models[0].user396
fits[0].fit_unit1/A
fits[0].fit_plothttps://www.sasbdb.org/media/fitting_files/scattering_plots/SASDXH4_fit1_fixed_fit_img.png
fits[0].softwareSREFLEX
fits[0].chi_square_value1.073
fits[0].p_value0.1937
fits[0].fit_residual_plotSASDXH4_fit1_fitresiduals_img.png
fits[0].fit_datahttps://www.sasbdb.org/media/fitting_files/SASDXH4_fit1.fit
fits[0].fit_lognull
fits[0].software_version4.0
fits[0].description
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fits[1].models[0].softwareDAMMIN
fits[1].models[0].pdb_link[]
fits[1].models[0].model_titlenull
fits[1].models[0].type_of_modeldummy
fits[1].models[0].software_version3.2.1
fits[1].models[0].model_datahttps://www.sasbdb.org/media/pdb_file/SASDXH4_fit2_model1.cif
fits[1].models[0].model_mwnull
fits[1].models[0].bead_radiusnull
fits[1].models[0].loghttps://www.sasbdb.org/media/log_files/DAMMINon_1983.log
fits[1].models[0].symmetrynull
fits[1].models[0].commentnull
fits[1].models[0].user396
fits[1].fit_unit1/A
fits[1].fit_plothttps://www.sasbdb.org/media/fitting_files/scattering_plots/SASDXH4_fit2_fixed_fit_img.png
fits[1].softwareDAMMIN
fits[1].chi_square_value1.004
fits[1].p_value0.6037
fits[1].fit_residual_plotSASDXH4_fit2_fitresiduals_img.png
fits[1].fit_datahttps://www.sasbdb.org/media/fitting_files/SASDXH4_fit2.fir
fits[1].fit_lognull
fits[1].software_version3.2.1
fits[1].description
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_versionnull
i0_calibration_standardnull
descriptionThe molecular weight estimate is an approximation; the actual molecular weight can vary depending on the specific glycosylation patterns and modifications of the IgE molecule. In this way, the estimated MW for the complex (including the theProfilin) is approximately 240 kDa. For the model for IgE structure, we developed a hybrid model inspired by Jansen et al., 2020. This model incorporates two Fab regions (allergen excluded) from the crystallographic structure (PDB entry 7SBD), combined with an extended human Fc fragment (CH2-CH3-CH4) from PDB entry 4J4P. The hybrid model was manually fitted into a low-resolution SAXS envelope obtained by using the DAMMIF, DAMAVER, and DAMMIN programs (SASBDB entry SASDVG9). This model for IgE was used to generate the IgE complex with the allergen (Profilin) using crystallographic structure (PDB entry 7SBD) fitting a low-resolution SAXS envelope obtained by DAMMIN program. Further refinement of the hybrid model was conducted through Normal Mode Analysis (NMA) using the SREFLEX program based on experimental SAXS data.
experiment_descriptionSynchrotron SAXS data from solutions of Mouse complex murine Immunoglobulin E (IgE) antibody with profilin (ration 1:3) in 20 mM Tris, 50 mM NaCl, pH 8.4 were collected on the P12 beamline at the DESY (Hamburg, Germany) using a Pilatus 6M-Dectris detector at a sample-detector distance of 3.0 m and a wavelength of λ = 0.124 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). In-line size-exclusion chromatography (SEC) SAS was employed. The SEC parameters were as follows: A 50.00 μl sample at 6.0 mg/ml was injected at a 0.75 ml/min flow rate onto a GE Superdex 200 Increase 10/300 column at 15°C. 3000 successive 1.0-second frames were collected. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted.
tags[]
intensity_unit1/cm
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manifest.json:34 field values
Field pathRaw value
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View the complete summary.json source
{
  "code": "SASDXH4",
  "status": "Published",
  "type_of_curve": "SEC-SAS",
  "angular_unit": "1/nm",
  "project": {
    "title": "Allergen-induced structural rearrangements in IgE: insights from SAXS and molecular dynamics.",
    "publication": {
      "title": "Allergen-induced structural rearrangements in IgE: insights from SAXS and molecular dynamics.",
      "author_list": "Gómez-Velasco H, García-Ramírez B, Siliqi D, Graewert MA, Quintero-Martinez A, Ortega E, Rodríguez-Romero A",
      "journal": "Int J Biol Macromol",
      "doi": "10.1016/j.ijbiomac.2025.147658",
      "pmid": "40953619",
      "published_date": "2025 Sep 13"
    },
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    "submitted_date": "2025-05-07",
    "released_date": "2025-09-17"
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            "address": "Bari, Italy",
            "full_name": "CNR - Institute of Crystallography, Bari, Italy",
            "webpage": "http://www.ba.ic.cnr.it"
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        "contributor_name": "Dritan",
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View the complete manifest.json source
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