SASDVG9

Mouse murine Immunoglobulin E (IgE) antibodies

Data type: SASBDB experimental data Status: Published Curve type: SEC-SAS Last updated: 2025-09-17T10:12:44.328913+02:00

Synchrotron SAXS data from solutions of murine IgE in 20 mM Tris, 50 mM NaCl, pH 8.4 were collected on the B21 beamline at Diamond (Didcot, UK) using an EigerX 4M-Detrics detector at a sample-detector distance of 3.7 m and the wavelength of 0.95 A. In-line size-exclusion chromatography (SEC) SAXS was employed. The SEC parameters were as follows: A 50.00 μl sample at 6.4 mg/ml was injected at a 0.075 ml/min flow rate onto a GE Superdex 200 Increase 10/300 column at 15°C and 620 successive 3-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. The molecular weight of a murine IgE, considering glycosylation, is approximately 190-198 kDa (protein 180 kDa + 10-18 kDa glycosylation). This estimate is an approximation; the actual molecular weight can vary depending on the specific glycosylation patterns and modifications of the IgE molecule.

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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · Mouse murine Immunoglobulin E (IgE) antibodies

Concentration— – 6.4 Buffer / pH20 mM Tris, 50 mM NaCl / 8.4
Experimental temperature15.0 Facility / beamlineDiamond Light Source / B21
Wavelength0.094 nmExposure3.0 s × 620

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
Murine Immunoglobulin E (IgE) antibodies
View sequence
EVQLVESGGGLVQPKGSLKLSCAASGFTFNTYAMNWVRQAPGKGLEWVARIRTKTNNYVTYYADSVKDRFTISRDDSQSMLYLQMNNLKTEDTAMYYCVRHVGDYWGQGTSVTVSSASIRNPQLYPLKPCKSMTLGCLVKDYFPGPVTVTWYSDSLNMSTVNFPALGSELKVTTSQVTSWGKSAKNFTCHVTHPPSFNESRTILVRPVNITEPTLELLHSSCDPNAFHSTIQLYCFIYGHILNDVSVSWLMDDREITDTLAQTVLIKEEGKLASTCSKLNITEQQWMSESTFTCKVTSQGVDYLAHTRRCPDHEPRGVITYLIPPSPLDLYQNGAPKLTCLVVDLESEKNVNVTWNQEKKTSVSASQWYTKHHNNATTSITSILPVVAKDWIEGYGYQCIVDHPDFPKPIVRSITKTPGQRSAPEVYVFPPPEEESEDKRTLTCLIQNFFPEDISVQWLGDGKLISNSQHSTTTPLKSNGSNQGFFIFSRLEVAKTLWTQRKQFTCQVIHEALQKPRKLEKTISTSDIQMTQSPASLSASVGETVTITCRASGNIHNYLAWFQQKQGKSPQLLVYNAKTLADGVPSRFSGSGSGTQYSLKINSLQPEDFGSYYCQHFWSTPYTFGGGTKLEIKRADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPKDINVKWKIDGSERQNGVLNSWTDQDSKDSTYSMSSTLTLTKDEYERHNSYTCEATHKTSTSPIVKSFNRNEEVQLVESGGGLVQPKGSLKLSCAASGFTFNTYAMNWVRQAPGKGLEWVARIRTKTNNYVTYYADSVKDRFTISRDDSQSMLYLQMNNLKTEDTAMYYCVRHVGDYWGQGTSVTVSSASIRNPQLYPLKPCKSMTLGCLVKDYFPGPVTVTWYSDSLNMSTVNFPALGSELKVTTSQVTSWGKSAKNFTCHVTHPPSFNESRTILVRPVNITEPTLELLHSSCDPNAFHSTIQLYCFIYGHILNDVSVSWLMDDREITDTLAQTVLIKEEGKLASTCSKLNITEQQWMSESTFTCKVTSQGVDYLAHTRRCPDHEPRGVITYLIPPSPLDLYQNGAPKLTCLVVDLESEKNVNVTWNQEKKTSVSASQWYTKHHNNATTSITSILPVVAKDWIEGYGYQCIVDHPDFPKPIVRSITKTPGQRSAPEVYVFPPPEEESEDKRTLTCLIQNFFPEDISVQWLGDGKLISNSQHSTTTPLKSNGSNQGFFIFSRLEVAKTLWTQRKQFTCQVIHEALQKPRKLEKTISTSLDIQMTQSPASLSASVGETVTITCRASGNIHNYLAWFQQKQGKSPQLLVYNAKTLADGVPSRFSGSGSGTQYSLKINSLQPEDFGSYYCQHFWSTPYTFGGGTKLEIKRADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPKDINVKWKIDGSERQNGVLNSWTDQDSKDSTYSMSSTLTLTKDEYERHNSYTCEATHKTSTSPIVKSFNRNE
proteinMus musculus——–—monomerMolecule count 1165.383 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
12573[3]0.0045–0.34 1/AHas uncertainty columnMissing 0111sasbdb/entries/g9/sasdvg9/source/SASDVG9.dat
▼

2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)19.2—Å
i0Guinier0.200696—1/cm
i0P(r)1.607836—1/cm
mwExperimental190.0—kDa
mwPorod240.0—kDa
porod_volumePorod422.0—ų
rgGuinier5.50.188Å
rgP(r)5.49—Å

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

▼

3. Source Fits and Models Source Fits & Models

▶

4. Source File Index Source Files

▶

5. Experiment Description and Publication Experiment & Publication

▼

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 date2024-10-03Storage / measurement temperature4.0 / 15.0
Exposure time3.0Frames620
Wavelength0.094Sample-to-detector distance3.7
SourceX-ray synchrotronDetectorEiger 4M
Facility / beamlineDiamond Light Source / B21 · Didcot, UK
q range0.045 – 3.4Sample volume / flow rate50.0 / 0.07

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:156 field values
Field pathRaw value
codeSASDVG9
statusPublished
type_of_curveSEC-SAS
angular_unit1/A
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
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experiment.instrument.detector.typenull
experiment.instrument.detector.nameEiger 4M
experiment.instrument.detector.resolution75.0
experiment.instrument.nameDiamond Light Source
experiment.instrument.cityDidcot
experiment.instrument.countryUK
experiment.instrument.beamline_nameB21
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.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 murine Immunoglobulin E (IgE) antibodies
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.date2024-10-03
experiment.storage_temperature4.0
experiment.cell_temperature15.0
experiment.exposure_time3.0
experiment.number_of_frames620
experiment.wavelength0.094
experiment.sample_detector_distance3.7
experiment.concentration_minnull
experiment.concentration_max6.4
experiment.sample_volume50.0
experiment.flow_rate0.07
experiment.s_min0.045
experiment.s_max3.4
experiment.total_exposure_timenull
experiment.seccolumn1
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fits[0].models[0].softwareDAMMIN
fits[0].models[0].pdb_link[]
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fits[0].models[0].user396
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fits[0].p_value0.0
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fits[0].description
estimated_volume_methodnull
pddf_softwareScÅtter
pddf_software_versionnull
i0_calibration_standardnull
descriptionSynchrotron SAXS data from solutions of murine IgE in 20 mM Tris, 50 mM NaCl, pH 8.4 were collected on the B21 beamline at Diamond (Didcot, UK) using an EigerX 4M-Detrics detector at a sample-detector distance of 3.7 m and the wavelength of 0.95 A. In-line size-exclusion chromatography (SEC) SAXS was employed. The SEC parameters were as follows: A 50.00 μl sample at 6.4 mg/ml was injected at a 0.075 ml/min flow rate onto a GE Superdex 200 Increase 10/300 column at 15°C and 620 successive 3-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. The molecular weight of a murine IgE, considering glycosylation, is approximately 190-198 kDa (protein 180 kDa + 10-18 kDa glycosylation). This estimate is an approximation; the actual molecular weight can vary depending on the specific glycosylation patterns and modifications of the IgE molecule.
experiment_descriptionnull
tags[]
intensity_unit1/cm
experimental_mw190.0
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mw240.0
porod_mw_errornull
pddf_i01.607836
pddf_i0_errornull
guinier_i00.200696
guinier_i0_errornull
pddf_rg5.49
pddf_rg_errornull
guinier_rg5.5
guinier_rg_error0.188
pddf_dmax19.2
pddf_dmax_errornull
porod_volume422.0
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first29
guinier_point_last96
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDVG9_datloglog_img.png
symmetrynull
last_modified2025-09-17T10:12:44.328913+02:00
bragg_peak[]
manifest.json:34 field values
Field pathRaw value
codeSASDVG9
statussuccess
started_at2026-08-11T16:34:35.806892+00:00
finished_at2026-08-11T16:34:43.932300+00:00
source_last_modified2025-09-17T10:12:44.328913+02:00
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View the complete summary.json source
{
  "code": "SASDVG9",
  "status": "Published",
  "type_of_curve": "SEC-SAS",
  "angular_unit": "1/A",
  "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"
    },
    "status": "released",
    "submitted_date": "2025-05-07",
    "released_date": "2025-09-17"
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  "pddf_data": "https://www.sasbdb.org/media/p_of_R_files/SASDVG9.dat",
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          "oligomerization": "monomer",
          "molecular_type": "protein",
          "uniprot_sequence": "",
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      "deuteration": null,
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    "contributor": [
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        "affiliation": [
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            "short_name": null,
            "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",
        "contributor_surname": "Siliqi",
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    "concentration_method": null,
    "concentration_unit": null,
    "date": "2024-10-03",
    "storage_temperature": 4.0,
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  "last_modified": "2025-09-17T10:12:44.328913+02:00",
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}
View the complete manifest.json source
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