SASDFP8

Carbonic anhydrase 2 from bovine erythrocytes - 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

Carbonic anhydrase underwent pre-purification prior to SEC-SAXS using the following method. All procedures were performed at 4 oC. The protein (from Sigma; Gel Filtration Markers Kit MWGF1000) was made to approximately 25 mg/ml 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 Superdex 75 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 (3 kDa centrifuge spin filter) to a final concentration of 11.9 mg/ml (the concentration was determined from triplicate UV A280 measurements using an E0.1% of 1.732 (= 1 g/l) calculated from the amino acid sequence (ProtParam)). Approximately 50 μl aliquots were snap-frozen in liquid nitrogen then stored at -80oC 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 2.4 nm.

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1. Samples, Components and Experimental Conditions Sample & Experiment

Sample 1 · Carbonic anhydrase 2 from bovine erythrocytes - SEC-SAXS coupled to multiangle laser and quasi-elastic light scattering (MALLS and QELS)

Concentration— – 11.9 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 × 41

Molecular Components

ComponentType / organismUniProt and ConstructOligomeric StateMolecular weight
Carbonic anhydrase 2
View sequence
MSHHWGYGKHNGPEHWHKDFPIANGERQSPVDIDTKAVVQDPALKPLALVYGEATSRRMVNNGHSFNVEYDDSQDKAVLKDGPLTGTYRLVQFHFHWGSSDDQGSEHTVDRKKYAAELHLVHWNTKYGDFGTAAQQPDGLAVVGVFLKVGDANPALQKVLDALDSIKTKGKSTDFPNFDPGSLLPNVLDYWTYPGSLTTPPLLESVTWIVLKEPISVSSQQMLKFRTLNFNAEGEPELLMLANWRPAQPLKNRQVRGFPK
proteinBos taurusP009211–260monomerMolecule count 129.113 kDa

Experimental Curves

CurvePoints / columnsq rangeUncertainty qualityNegative-intensity pointsSource file
12584[3]0.072981–7.21299 1/nmHas uncertainty columnMissing 016sasbdb/entries/p8/sasdfp8/source/SASDFP8.dat
▼

2. Measurements Reported by SASBDB Reported Results

MetricMethodValueUncertaintyUnit
dmaxP(r)5.05—nm
i0Guinier7753.83.15arbitrary
i0P(r)7744.02.5arbitrary
mwExperimental28.3—kDa
mwPorod23.0—kDa
porod_volumePorod36.7—nm³
rgGuinier1.82—nm
rgP(r)1.7920.001nm

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

▼

3. Source Fits and Models Source Fits & Models

Fit 1 · DAMMIN

χ²: 1.02CorMap p: 0.448891Unit: 1/A

Fit of refined DAMMIN model obtained from the spatial alignment of 10 individual models that fit the SAXS data.

ModelName / TypeSoftwareSymmetryModel MWPDB DeclarationSource file
1—dummyDAMMIN SUPCOMB 23 (r9988)P122.648—Model Image
2—dummyDAMFILT DAMFILT 5.0 (r10552)P122.209—Model Image

Fit 2 · CRYSOL CRYSOL_30

χ²: 1.095CorMap p: 0.269894Unit: 1/A

CRYSOL_30 fit calculated with 30 harmonics and 300 points

ModelName / TypeSoftwareSymmetryModel MWPDB DeclarationSource file
1—atomicPDB (Protein Data Bank) P128.965A25Model 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 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 time1.0Frames41
Wavelength0.123982Sample-to-detector distance3.0
SourceX-ray synchrotronDetectorPilatus 6M
Facility / beamlinePETRA III / EMBL P12 · DESY; Hamburg, Germany
q range0.073 – 7.213Sample volume / flow rate100.0 / 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

CategoryFileStatusSizeChecksumDownload and View
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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:202 field values
Field pathRaw value
codeSASDFP8
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/SASDFP8.out
intensities_datahttps://www.sasbdb.org/media/intensities_files/SASDFP8.dat
intensities_log_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDFP8_dat_img.png
intensities_kratky_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDFP8_kratky_img.png
pddf_plothttps://www.sasbdb.org/media/p_of_R_files/pofr_images/SASDFP8_pofr_img.png
intensities_guinier_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDFP8_guinier_img.png
sascif_datahttps://www.sasbdb.org/media/sascif/sascif_files/SASDFP8.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_nameCarbonic anhydrase 2
experiment.sample.molecule[0].short_nameCA2
experiment.sample.molecule[0].sequenceMSHHWGYGKHNGPEHWHKDFPIANGERQSPVDIDTKAVVQDPALKPLALVYGEATSRRMV NNGHSFNVEYDDSQDKAVLKDGPLTGTYRLVQFHFHWGSSDDQGSEHTVDRKKYAAELHL VHWNTKYGDFGTAAQQPDGLAVVGVFLKVGDANPALQKVLDALDSIKTKGKSTDFPNFDP GSLLPNVLDYWTYPGSLTTPPLLESVTWIVLKEPISVSSQQMLKFRTLNFNAEGEPELLM LANWRPAQPLKNRQVRGFPK
experiment.sample.molecule[0].organismBos taurus
experiment.sample.molecule[0].uniprot_codeP00921
experiment.sample.molecule[0].uniprot_range_first1
experiment.sample.molecule[0].uniprot_range_last260
experiment.sample.molecule[0].oligomerizationmonomer
experiment.sample.molecule[0].molecular_typeprotein
experiment.sample.molecule[0].uniprot_sequenceMSHHWGYGKHNGPEHWHKDFPIANGERQSPVDIDTKAVVQDPALKPLALVYGEATSRRMV NNGHSFNVEYDDSQDKAVLKDGPLTGTYRLVQFHFHWGSSDDQGSEHTVDRKKYAAELHL VHWNTKYGDFGTAAQQPDGLAVVGVFLKVGDANPALQKVLDALDSIKTKGKSTDFPNFDP GSLLPNVLDYWTYPGSLTTPPLLESVTWIVLKEPISVSSQQMLKFRTLNFNAEGEPELLM LANWRPAQPLKNRQVRGFPK
experiment.sample.molecule[0].mw29.113
experiment.sample.molecule[0].total_mw29.113
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_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.nameCarbonic anhydrase 2 from bovine erythrocytes - 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_frames41
experiment.wavelength0.123982
experiment.sample_detector_distance3.0
experiment.concentration_minnull
experiment.concentration_max11.9
experiment.sample_volume100.0
experiment.flow_rate0.5
experiment.s_min0.073
experiment.s_max7.213
experiment.total_exposure_timenull
experiment.seccolumn3
fits[0].models[0].model_plothttps://www.sasbdb.org/media/pdb_file/images/SASDFP8_fit1_model1_img.png
fits[0].models[0].softwareDAMMIN
fits[0].models[0].pdb_link[]
fits[0].models[0].model_titlenull
fits[0].models[0].type_of_modeldummy
fits[0].models[0].software_versionSUPCOMB 23 (r9988)
fits[0].models[0].model_datahttps://www.sasbdb.org/media/pdb_file/SASDFP8_fit1_model1.pdb
fits[0].models[0].model_mw22.648
fits[0].models[0].bead_radius1.5
fits[0].models[0].lognull
fits[0].models[0].symmetryP1
fits[0].models[0].commentRefined DAMMIN model obtained from the spatial alignment of 10 individual models (DAMSTART)
fits[0].models[0].user9
fits[0].models[1].model_plothttps://www.sasbdb.org/media/pdb_file/images/SASDFP8_fit1_model2_img.png
fits[0].models[1].softwareDAMFILT
fits[0].models[1].pdb_link[]
fits[0].models[1].model_titlenull
fits[0].models[1].type_of_modeldummy
fits[0].models[1].software_versionDAMFILT 5.0 (r10552)
fits[0].models[1].model_datahttps://www.sasbdb.org/media/pdb_file/SASDFP8_fit1_model2.pdb
fits[0].models[1].model_mw22.209
fits[0].models[1].bead_radius1.5
fits[0].models[1].lognull
fits[0].models[1].symmetryP1
fits[0].models[1].commentDAMFILT spatially aligned and volume occupancy corrected (averaged) model from 10 individual models
fits[0].models[1].user9
fits[0].fit_unit1/A
fits[0].fit_plothttps://www.sasbdb.org/media/fitting_files/scattering_plots/SASDFP8_fit1_fixed_fit_img.png
fits[0].softwareDAMMIN
fits[0].chi_square_value1.02
fits[0].p_value0.448891
fits[0].fit_residual_plotSASDFP8_fit1_fitresiduals_img.png
fits[0].fit_datahttps://www.sasbdb.org/media/fitting_files/SASDFP8_fit1.fir
fits[0].fit_loghttps://www.sasbdb.org/media/fitting_files/log_files/refine_0U0OuhM.log
fits[0].software_versionnull
fits[0].descriptionFit of refined DAMMIN model obtained from the spatial alignment of 10 individual models that fit the SAXS data.
fits[1].models[0].model_plothttps://www.sasbdb.org/media/pdb_file/images/SASDFP8_fit2_model1_img.png
fits[1].models[0].softwarePDB (Protein Data Bank)
fits[1].models[0].pdb_link[0].pdb_code5a25
fits[1].models[0].pdb_link[0].ext_code5A25
fits[1].models[0].pdb_link[0].ext_typepdb
fits[1].models[0].pdb_link[0].difference_with_modelderived
fits[1].models[0].model_titlenull
fits[1].models[0].type_of_modelatomic
fits[1].models[0].software_versionnull
fits[1].models[0].model_datahttps://www.sasbdb.org/media/pdb_file/SASDFP8_fit2_model1.pdb
fits[1].models[0].model_mw28.96
fits[1].models[0].bead_radiusnull
fits[1].models[0].lognull
fits[1].models[0].symmetryP1
fits[1].models[0].commentModel-fit calculated using 30 harmonics and 300 points
fits[1].models[0].user9
fits[1].fit_unit1/A
fits[1].fit_plothttps://www.sasbdb.org/media/fitting_files/scattering_plots/SASDFP8_fit2_fixed_fit_img.png
fits[1].softwareCRYSOL
fits[1].chi_square_value1.095
fits[1].p_value0.269894
fits[1].fit_residual_plotSASDFP8_fit2_fitresiduals_img.png
fits[1].fit_datahttps://www.sasbdb.org/media/fitting_files/SASDFP8_fit2.fit
fits[1].fit_loghttps://www.sasbdb.org/media/fitting_files/log_files/5a25_monomerr00.log
fits[1].software_versionCRYSOL_30
fits[1].descriptionCRYSOL_30 fit calculated with 30 harmonics and 300 points
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_version5.0
i0_calibration_standardnull
descriptionCarbonic anhydrase underwent pre-purification prior to SEC-SAXS using the following method. All procedures were performed at 4 oC. The protein (from Sigma; Gel Filtration Markers Kit MWGF1000) was made to approximately 25 mg/ml 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 Superdex 75 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 (3 kDa centrifuge spin filter) to a final concentration of 11.9 mg/ml (the concentration was determined from triplicate UV A280 measurements using an E0.1% of 1.732 (= 1 g/l) calculated from the amino acid sequence (ProtParam)). Approximately 50 μl aliquots were snap-frozen in liquid nitrogen then stored at -80oC 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 2.4 nm.
experiment_descriptionSynchrotron SAXS data from carbonic anhydrase 2 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 100.00 μl sample at 11.9 mg/ml was injected at a 0.50 ml/min flow rate onto a GE Superdex 75 Increase 10/300 column at 20°C. 41 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_mw28.3
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mw23.0
porod_mw_errornull
pddf_i07744.0
pddf_i0_error2.5
guinier_i07753.8
guinier_i0_error3.15
pddf_rg1.792
pddf_rg_error0.001
guinier_rg1.82
guinier_rg_errornull
pddf_dmax5.05
pddf_dmax_errornull
porod_volume36.7
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first1
guinier_point_last231
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDFP8_datloglog_img.png
symmetrynull
last_modified2023-06-21T07:55:24.740692+02:00
bragg_peak[]
manifest.json:36 field values
Field pathRaw value
codeSASDFP8
statussuccess
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View the complete summary.json source
{
  "code": "SASDFP8",
  "status": "Published",
  "type_of_curve": "SEC-SAS",
  "angular_unit": "1/nm",
  "project": {
    "title": "Adding Size Exclusion Chromatography (SEC) and Light Scattering (LS) Devices to Obtain High-Quality Small Angle X-Ray Scattering (SAXS) Data",
    "publication": {
      "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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    "released_date": "2019-07-10"
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          "long_name": "Carbonic anhydrase 2",
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      "name": "Carbonic anhydrase 2 from bovine erythrocytes - SEC-SAXS coupled to multiangle laser and quasi-elastic light scattering (MALLS and QELS)",
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    "contributor": [
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        "affiliation": [
          {
            "short_name": "EMBL-Hamburg",
            "address": "Notkestraße 85, Geb. 25A, 22607 Hamburg, Deutschland, Germany",
            "full_name": "European Molecular Biology Laboratory (EMBL) - Hamburg outstation",
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        "contributor_name": "Melissa ",
        "contributor_surname": "Graewert",
        "orcid": null
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            "short_name": "EMBL-Hamburg",
            "address": "Notkestraße 85, Geb. 25A, 22607 Hamburg, Deutschland, Germany",
            "full_name": "European Molecular Biology Laboratory (EMBL) - Hamburg outstation",
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View the complete manifest.json source
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