SASDFN8

Apoferritin from horse spleen - SEC-SAXS coupled to multiangle laser and quasi-elastic light scattering (MALLS and QELS)

Data type: SASBDB experimental data Status: Published Curve type: SEC-SAS Last updated: 2023-06-21T07:55:24.740692+02:00

Apoferritin underwent pre-purification prior SEC-SAXS using the following method. All procedures were performed at 4 oC. An apoferritin stock solution (from equine spleen supplied in ca. 50% v/v glycerol; Sigma Gel Filtration Markers Kit MWGF1000) was diluted two-fold in 25 mM HEPES, 50 mM NaCl, 5 mM urea, 1% v/v glycerol, pH 7. Approximately 200 μl of sample were loaded onto a Superose 6 Increase 10/300 column (GE Healthcare) equilibrated in the same buffer (flow rate = 0.4 ml/min). Fractionated aliquots corresponding to the highest absorbing peak (estimated using UV A280 and UV A245 nm) were pooled and concentrated (30 kDa centrifuge spin filter) to a final concentration of 11 mg/ml (the concentration was determined from triplicate UV A280 measurements using an E0.1% of 0.729 (= 1 g/l) calculated from the amino acid sequence (ProtParam)). Approximately 50 μl aliquots were snap-frozen in liquid nitrogen then stored at -80 oC prior to the SEC-SAXS analysis that was performed at room temperature in 50 mM HEPES, 150 mM NaCl, 2% v/v glycerol, pH 7. The Rg-correlation through the SEC-SAXS peak, the individual unsubtracted SEC-SAXS frames as well as the results from coupled MALLS and QELS analysis are included in the full entry zip archive. The quoted experimental molecular weight was determined using MALLS in combination with refractive-index (RI) measurements that were recorded from the same sample eluting from the column using a split-flow SEC-SAXS-light scattering configuration (Graewert et al., (2015) Sci. Reports. 5, 10734: doi: 10.1038/srep10734). The average hydrodynamic radius of the protein is 6.7 nm.

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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · Apoferritin from horse spleen - SEC-SAXS coupled to multiangle laser and quasi-elastic light scattering (MALLS and QELS)

Concentration— – 11.0 Buffer / pH50 mM HEPES, 150 mM NaCl, 2% v/v glycerol / 7.0
Experimental temperature20.0 Facility / beamlinePETRA III / EMBL P12
Wavelength0.123982 nmExposure1.0 s × 85

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
Apoferritin light chain
View sequence
MSSQIRQNYSTEVEAAVNRLVNLYLRASYTYLSLGFYFDRDDVALEGVCHFFRELAEEKREGAERLLKMQNQRGGRALFQDLQKPSQDEWGTTLDAMKAAIVLEKSLNQALLDLHALGSAQADPHLCDFLESHFLDEEVKLIKKMGDHLTNIQRLVGSQAGLGEYLFERLTLKHD
proteinEquus caballusP027911–17524-merMolecule count 2419.977 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
12577[3]0.0923306–7.21299 1/nmHas uncertainty columnMissing 02sasbdb/entries/n8/sasdfn8/source/SASDFN8.dat
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2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)12.5—nm
i0Guinier50957.821.0arbitrary
i0P(r)50700.0—arbitrary
mwExperimental454.0—kDa
mwPorod424.0—kDa
porod_volumePorod679.0—nm³
rgGuinier5.35—nm
rgP(r)5.222—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

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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 name50 mM HEPES, 150 mM NaCl, 2% v/v glycerolBuffer concentration—
pH7.0Additives—
Buffer descriptionRunning buffer for SEC-SAXS
Purity measurement method—Extinction coefficient—
Absorbance—Scattering contrast—
Specific volume / dry volume— / —Mixture / deuteration— / —

Acquisition Conditions and Instrument

Measurement date2019-04-05Storage / measurement temperature20.0 / 20.0
Exposure time1.0Frames85
Wavelength0.123982Sample-to-detector distance3.0
SourceX-ray synchrotronDetectorPilatus 6M
Facility / beamlinePETRA III / EMBL P12 · DESY; Hamburg, Germany
q range0.092 – 7.213Sample volume / flow rate50.0 / 0.5

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:225 field values
Field pathRaw value
codeSASDFN8
statusPublished
type_of_curveSEC-SAS
angular_unit1/nm
project.titleAdding Size Exclusion Chromatography (SEC) and Light Scattering (LS) Devices to Obtain High-Quality Small Angle X-Ray Scattering (SAXS) Data
project.publication.titleAdding Size Exclusion Chromatography (SEC) and Light Scattering (LS) Devices to Obtain High-Quality Small Angle X-Ray Scattering (SAXS) Data
project.publication.author_listGraewert M, Da Vela S, Gräwert T, Molodenskiy D, Blanchet C, Svergun D, Jeffries C
project.publication.journalCrystals
project.publication.doi10.3390/cryst10110975
project.publication.pmidnull
project.publication.published_date2020 Oct 27
project.statusreleased
project.submitted_date2019-07-10
project.released_date2019-07-10
pddf_datahttps://www.sasbdb.org/media/p_of_R_files/SASDFN8.out
intensities_datahttps://www.sasbdb.org/media/intensities_files/SASDFN8.dat
intensities_log_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDFN8_dat_img.png
intensities_kratky_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDFN8_kratky_img.png
pddf_plothttps://www.sasbdb.org/media/p_of_R_files/pofr_images/SASDFN8_pofr_img.png
intensities_guinier_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDFN8_guinier_img.png
sascif_datahttps://www.sasbdb.org/media/sascif/sascif_files/SASDFN8.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_nameApoferritin light chain
experiment.sample.molecule[0].short_namenull
experiment.sample.molecule[0].sequenceMSSQIRQNYSTEVEAAVNRLVNLYLRASYTYLSLGFYFDRDDVALEGVCHFFRELAEEKR EGAERLLKMQNQRGGRALFQDLQKPSQDEWGTTLDAMKAAIVLEKSLNQALLDLHALGSA QADPHLCDFLESHFLDEEVKLIKKMGDHLTNIQRLVGSQAGLGEYLFERLTLKHD
experiment.sample.molecule[0].organismEquus caballus
experiment.sample.molecule[0].uniprot_codeP02791
experiment.sample.molecule[0].uniprot_range_first1
experiment.sample.molecule[0].uniprot_range_last175
experiment.sample.molecule[0].oligomerization24-mer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMSSQIRQNYSTEVEAAVNRLVNLYLRASYTYLSLGFYFDRDDVALEGVCHFFRELAEEKR EGAERLLKMQNQRGGRALFQDLQKPSQDEWGTTLDAMKAAIVLEKSLNQALLDLHALGSA QADPHLCDFLESHFLDEEVKLIKKMGDHLTNIQRLVGSQAGLGEYLFERLTLKHD
experiment.sample.molecule[0].mw19.977
experiment.sample.molecule[0].total_mw479.448
experiment.sample.molecule[0].number_molecules24
experiment.sample.molecule[0].complex_stateFalse
experiment.sample.molecule[0].deuterationnull
experiment.sample.molecule[0].molecule_sourcebiological
experiment.sample.molecule[0].molecule_descriptionnull
experiment.sample.buffer.name50 mM HEPES, 150 mM NaCl, 2% v/v glycerol
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentRunning buffer for SEC-SAXS
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph7.0
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameApoferritin from horse spleen - SEC-SAXS coupled to multiangle laser and quasi-elastic light scattering (MALLS and QELS)
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_nameEMBL-Hamburg
experiment.contributor[0].affiliation[0].addressNotkestraße 85, Geb. 25A, 22607 Hamburg, Deutschland, Germany
experiment.contributor[0].affiliation[0].full_nameEuropean Molecular Biology Laboratory (EMBL) - Hamburg outstation
experiment.contributor[0].affiliation[0].webpagehttp://www.embl-hamburg.de/index.php
experiment.contributor[0].contributor_nameMelissa
experiment.contributor[0].contributor_surnameGraewert
experiment.contributor[0].orcidnull
experiment.contributor[1].affiliation[0].short_nameEMBL-Hamburg
experiment.contributor[1].affiliation[0].addressNotkestraße 85, Geb. 25A, 22607 Hamburg, Deutschland, Germany
experiment.contributor[1].affiliation[0].full_nameEuropean Molecular Biology Laboratory (EMBL) - Hamburg outstation
experiment.contributor[1].affiliation[0].webpagehttp://www.embl-hamburg.de/index.php
experiment.contributor[1].contributor_nameCy M
experiment.contributor[1].contributor_surnameJeffries
experiment.contributor[1].orcidnull
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2019-04-05
experiment.storage_temperature20.0
experiment.cell_temperature20.0
experiment.exposure_time1.0
experiment.number_of_frames85
experiment.wavelength0.123982
experiment.sample_detector_distance3.0
experiment.concentration_minnull
experiment.concentration_max11.0
experiment.sample_volume50.0
experiment.flow_rate0.5
experiment.s_min0.092
experiment.s_max7.213
experiment.total_exposure_timenull
experiment.seccolumn1
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fits[0].models[1].lognull
fits[0].models[1].symmetrynull
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fits[0].chi_square_value1.074
fits[0].p_value0.57789
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fits[0].description
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fits[1].models[0].model_mwnull
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fits[1].models[0].lognull
fits[1].models[0].symmetryP432
fits[1].models[0].commentnull
fits[1].models[0].user9
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fits[1].softwareGASBOR
fits[1].chi_square_value5.88
fits[1].p_value0.0
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fits[1].description
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fits[2].models[0].softwarePDB (Protein Data Bank)
fits[2].models[0].pdb_link[0].pdb_code1ier
fits[2].models[0].pdb_link[0].ext_code1IER
fits[2].models[0].pdb_link[0].ext_typepdb
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fits[2].models[0].user9
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fits[2].softwareCRYSOL
fits[2].chi_square_value8.846
fits[2].p_value0.0
fits[2].fit_residual_plotSASDFN8_fit3_fitresiduals_img.png
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fits[2].fit_loghttps://www.sasbdb.org/media/fitting_files/log_files/1IER_derivedr00.log
fits[2].software_versionCRYSOL 30
fits[2].descriptionFit of PDB model 1IER
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionApoferritin underwent pre-purification prior SEC-SAXS using the following method. All procedures were performed at 4 oC. An apoferritin stock solution (from equine spleen supplied in ca. 50% v/v glycerol; Sigma Gel Filtration Markers Kit MWGF1000) was diluted two-fold in 25 mM HEPES, 50 mM NaCl, 5 mM urea, 1% v/v glycerol, pH 7. Approximately 200 μl of sample were loaded onto a Superose 6 Increase 10/300 column (GE Healthcare) equilibrated in the same buffer (flow rate = 0.4 ml/min). Fractionated aliquots corresponding to the highest absorbing peak (estimated using UV A280 and UV A245 nm) were pooled and concentrated (30 kDa centrifuge spin filter) to a final concentration of 11 mg/ml (the concentration was determined from triplicate UV A280 measurements using an E0.1% of 0.729 (= 1 g/l) calculated from the amino acid sequence (ProtParam)). Approximately 50 μl aliquots were snap-frozen in liquid nitrogen then stored at -80 oC prior to the SEC-SAXS analysis that was performed at room temperature in 50 mM HEPES, 150 mM NaCl, 2% v/v glycerol, pH 7. The Rg-correlation through the SEC-SAXS peak, the individual unsubtracted SEC-SAXS frames as well as the results from coupled MALLS and QELS analysis are included in the full entry zip archive. The quoted experimental molecular weight was determined using MALLS in combination with refractive-index (RI) measurements that were recorded from the same sample eluting from the column using a split-flow SEC-SAXS-light scattering configuration (Graewert et al., (2015) Sci. Reports. 5, 10734: doi: 10.1038/srep10734). The average hydrodynamic radius of the protein is 6.7 nm.
experiment_descriptionSynchrotron SAXS data from apoferritin in 50 mM HEPES, 150 mM NaCl, 2% v/v glycerol, pH 7 were collected on the EMBL P12 beam line at PETRA III (DESY, Hamburg, Germany) using a Pilatus 6M detector at a sample-detector distance of 3 m and at 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 11 mg/ml was injected at a 0.50 ml/min flow rate onto a GE Superdex 200 Increase 10/300 column at 20°C. 85 successive 1 second frames were collected through the major SEC-elution peak and processed using CHROMIXS. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted.
tags[0]benchmark
intensity_unitarbitrary
experimental_mw454.0
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mw424.0
porod_mw_errornull
pddf_i050700.0
pddf_i0_errornull
guinier_i050957.8
guinier_i0_error21.0
pddf_rg5.222
pddf_rg_errornull
guinier_rg5.35
guinier_rg_errornull
pddf_dmax12.5
pddf_dmax_errornull
porod_volume679.0
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first1
guinier_point_last52
pddf_point_firstnull
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Field pathRaw value
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View the complete summary.json source
{
  "code": "SASDFN8",
  "status": "Published",
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  "angular_unit": "1/nm",
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    "title": "Adding Size Exclusion Chromatography (SEC) and Light Scattering (LS) Devices to Obtain High-Quality Small Angle X-Ray Scattering (SAXS) Data",
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      "title": "Adding Size Exclusion Chromatography (SEC) and Light Scattering (LS) Devices to Obtain High-Quality Small Angle X-Ray Scattering (SAXS) Data",
      "author_list": "Graewert M, Da Vela S, Gräwert T, Molodenskiy D, Blanchet C, Svergun D, Jeffries C",
      "journal": "Crystals",
      "doi": "10.3390/cryst10110975",
      "pmid": null,
      "published_date": "2020 Oct 27"
    },
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    "submitted_date": "2019-07-10",
    "released_date": "2019-07-10"
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            "address": "Notkestraße 85, Geb. 25A, 22607 Hamburg, Deutschland, Germany",
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View the complete manifest.json source
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