SASDWV6

SEC-SAXS data for the monomeric (24mer) fraction of horse spleen apoferritin

数据类型:SASBDB 实验数据 状态:Published 曲线类型:SEC-SAS 最后更新:2026-02-04T12:11:49.985403+01:00

The preparation and analysis of horse spleen apoferritin were conducted to isolate its monomeric (24mer) and dimeric (2 x 24mer) forms and enable detailed structural characterization. Sample Preparation: Horse spleen apoferritin (purchased from Sigma-Aldrich, Merck KGaA, Germany), supplied with 50% v/v glycerol, was dialyzed overnight against 200 mM sodium acetate (pH 5.0). The dialyzed sample was then heated at 50°C for 5 hours, followed by centrifugation at 20,000 rcf for 15 minutes. The resulting supernatant was injected into a Superose 6 column (24 ml). Fractionation and Concentration: Fractions corresponding to apoferritin 24mer monomers were pooled and neutralized by adding an appropriate volume of 1M Tris (pH 8.0). The sample was concentrated to a final concentration of 22 mg/ml using a 100 kDa centrifuge spin filter and centrifuged again at 10,000 rcf for 10 minutes. Size Exclusion Chromatography and SAXS Analysis: Approximately 65 μl of the supernatant were loaded onto a Superose 6 Increase 10/300 column (GE Healthcare), equilibrated in DPBS buffer (137 mM NaCl, 2.7 mM KCl, 10 mM phosphate buffer, pH 7.4, 0.9 mM CaCl2, 0.5 mM MgCl2). The flow rate was set at 0.5 ml/min. SAXS frames corresponding to the monomeric 24mer fraction of apoferritin (elution volume range: 14.5–14.75 ml) with a constant Rg value were selected for further analysis.

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1. 样品、组分与实验条件 Sample & Experiment

样品 1 · SEC-SAXS data for the monomeric (24mer) fraction of horse spleen apoferritin

浓度— – 22.3 缓冲液 / pH137 mM NaCl, 2.7 mM KCl, 10 mM phosphate buffer, 0.9 mM CaCl2, 0.5 mM MgCl2 / 7.4
实验温度20.0 设备 / 束线Shanghai Synchrotron Radiation Facility (SSRF) / BL19U2
波长0.1033 nm曝光1.0 s × 40

分子组分

组分类型 / 物种UniProt 与构建体寡聚状态分子量
Ferritin light chain
查看序列
SSQIRQNYSTEVEAAVNRLVNLYLRASYTYLSLGFYFDRDDVALEGVCHFFRELAEEKREGAERLLKMQNQRGGRALFQDLQKPSQDEWGTTLDAMKAAIVLEKSLNQALLDLHALGSAQADPHLCDFLESHFLDEEVKLIKKMGDHLTNIQRLVGSQAGLGEYLFERLTLKHD
proteinEquus caballusP027912–17524-mer分子数 2419.846 kDa

实验曲线

曲线点数 / 列q 范围误差质量负强度点来源文件
11142[3]0.005798415–0.4067676 1/A含误差列缺失 01sasbdb/entries/v6/sasdwv6/source/SASDWV6.dat
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2. SASBDB 报告的指标 Reported Results

指标方法数值误差单位
dmaxP(r)13.5—Å
i0Guinier0.248256—1/cm
i0P(r)0.2464—1/cm
mwExperimental464.48—kDa
mwPorod537.91—kDa
porod_volumePorod650.81—ų
rgGuinier5.3850.056Å
rgP(r)5.24—Å

这些数值是 SASBDB 来源记录,不是 SAXSdb 对实验曲线重新计算的结果。

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3. 来源拟合与模型 Source Fits & Models

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4. 来源文件索引 Source Files

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5. 实验说明与论文 Experiment & Publication

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6. 完整来源记录 Complete Source Record

下列内容直接来自 SASBDB 条目。字段没有值时显示“—”;未声明的单位不会由 SAXSdb 猜测。

打开 SASBDB 原始条目

缓冲液与样品属性

缓冲液名称137 mM NaCl, 2.7 mM KCl, 10 mM phosphate buffer, 0.9 mM CaCl2, 0.5 mM MgCl2缓冲液浓度—
pH7.4添加剂—
缓冲液说明—
纯度测定方法—消光系数—
吸收值—散射对比度—
比体积 / 干体积— / —混合物 / 氘代— / —

采集条件与仪器

测量日期2024-05-24储存 / 测量温度4.0 / 20.0
曝光时间1.0帧数40
波长0.1033样品-探测器距离2.696
光源X-ray synchrotron探测器Pilatus 1M
机构 / 束线Shanghai Synchrotron Radiation Facility (SSRF) / BL19U2 · Shanghai, China
q 范围0.058 – 4.068样品体积 / 流速65.0 / 0.5

SASBDB 原始图

实验 I(q)
实验 I(q)
实验 I(q) log-log
实验 I(q) log-log
Guinier 图
Guinier 图
Kratky 图
Kratky 图
P(r) 图
P(r) 图

可下载文件

类别文件状态大小校验值下载与查看
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pddfsasbdb/entries/v6/sasdwv6/source/SASDWV6.outdownloaded66742f4721445053dca45855cda221b3deb0f79bf9b21b2cd7712338c17c40a65ceae下载查看原文件源站
sascifsasbdb/entries/v6/sasdwv6/source/SASDWV6.sascifnot_available——下载查看原文件源站
summarysasbdb/entries/v6/sasdwv6/source/summary.jsondownloaded88528ed939d6afff5113bd1cbedc4fdfebef797d8fbdc61c947c546b3535af6df3b2下载查看原文件源站
curve:来源记录
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full_entry_zip:来源记录与 ZIP 内部目录(4 项)
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pddf:来源记录
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sascif:来源记录
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summary:来源记录
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全部来源字段(无筛选)

这里自动展开来源记录中的每一个字段,包括空值、列表成员和页面上方已展示过的字段。

summary.json:154 个字段值
字段路径原始值
codeSASDWV6
statusPublished
type_of_curveSEC-SAS
angular_unit1/A
project.titleStructural insights into the nature of static and dynamic apoferritin dimers
project.publicationnull
project.statusreleased
project.submitted_date2025-01-28
project.released_date2026-01-28
pddf_datahttps://www.sasbdb.org/media/p_of_R_files/SASDWV6.out
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intensities_guinier_plothttps://www.sasbdb.org/media/intensities_files/scattering_plots/SASDWV6_guinier_img.png
sascif_datahttps://www.sasbdb.org/media/sascif/sascif_files/SASDWV6.sascif
experiment.instrument.detector.typeDectris
experiment.instrument.detector.namePilatus 1M
experiment.instrument.detector.resolution172.0
experiment.instrument.nameShanghai Synchrotron Radiation Facility (SSRF)
experiment.instrument.cityShanghai
experiment.instrument.countryChina
experiment.instrument.beamline_nameBL19U2
experiment.instrument.beam_geometry
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_nameFerritin light chain
experiment.sample.molecule[0].short_nameApoferritin monomer
experiment.sample.molecule[0].sequenceSSQIRQNYSTEVEAAVNRLVNLYLRASYTYLSLGFYFDRDDVALEGVCHFFRELAEEKREGAERLLKMQNQRGGRALFQDLQKPSQDEWGTTLDAMKAAIVLEKSLNQALLDLHALGSAQADPHLCDFLESHFLDEEVKLIKKMGDHLTNIQRLVGSQAGLGEYLFERLTLKHD
experiment.sample.molecule[0].organismEquus caballus
experiment.sample.molecule[0].uniprot_codeP02791
experiment.sample.molecule[0].uniprot_range_first2
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].mw19.846
experiment.sample.molecule[0].total_mw476.304
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_descriptionMonomer of horse spleen apoferritin
experiment.sample.buffer.name137 mM NaCl, 2.7 mM KCl, 10 mM phosphate buffer, 0.9 mM CaCl2, 0.5 mM MgCl2
experiment.sample.buffer.concentration_unitnull
experiment.sample.buffer.commentnull
experiment.sample.buffer.additivenull
experiment.sample.buffer.concentrationnull
experiment.sample.buffer.pkanull
experiment.sample.buffer.ph7.4
experiment.sample.buffer.deuterationnull
experiment.sample.purity_methodnull
experiment.sample.nameSEC-SAXS data for the monomeric (24mer) fraction of horse spleen apoferritin
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].addressnull
experiment.contributor[0].affiliation[0].full_nameUniversity of Groningen
experiment.contributor[0].affiliation[0].webpagenull
experiment.contributor[0].contributor_nameAleksei
experiment.contributor[0].contributor_surnameTsarenko
experiment.contributor[0].orcidhttps://orcid.org/0000-0002-4221-3317
experiment.concentration_methodnull
experiment.concentration_unitnull
experiment.date2024-05-24
experiment.storage_temperature4.0
experiment.cell_temperature20.0
experiment.exposure_time1.0
experiment.number_of_frames40
experiment.wavelength0.1033
experiment.sample_detector_distance2.696
experiment.concentration_minnull
experiment.concentration_max22.3
experiment.sample_volume65.0
experiment.flow_rate0.5
experiment.s_min0.058
experiment.s_max4.068
experiment.total_exposure_timenull
experiment.seccolumn5
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fits[0].models[0].softwareChimera
fits[0].models[0].pdb_link[0].pdb_code2w0o
fits[0].models[0].pdb_link[0].ext_code2W0O
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fits[0].models[0].software_version1.14
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fits[0].models[0].model_mw464.5
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].user1173
fits[0].fit_unit1/A
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fits[0].softwareCRYSOL
fits[0].chi_square_value14.583
fits[0].p_value0.0
fits[0].fit_residual_plotSASDWV6_fit1_fitresiduals_img.png
fits[0].fit_datahttps://www.sasbdb.org/media/fitting_files/SASDWV6_fit1.fit
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fits[0].software_version3.0
fits[0].description
estimated_volume_methodnull
pddf_softwareATSAS GNOM
pddf_software_versionnull
i0_calibration_standardnull
descriptionThe preparation and analysis of horse spleen apoferritin were conducted to isolate its monomeric (24mer) and dimeric (2 x 24mer) forms and enable detailed structural characterization. Sample Preparation: Horse spleen apoferritin (purchased from Sigma-Aldrich, Merck KGaA, Germany), supplied with 50% v/v glycerol, was dialyzed overnight against 200 mM sodium acetate (pH 5.0). The dialyzed sample was then heated at 50°C for 5 hours, followed by centrifugation at 20,000 rcf for 15 minutes. The resulting supernatant was injected into a Superose 6 column (24 ml). Fractionation and Concentration: Fractions corresponding to apoferritin 24mer monomers were pooled and neutralized by adding an appropriate volume of 1M Tris (pH 8.0). The sample was concentrated to a final concentration of 22 mg/ml using a 100 kDa centrifuge spin filter and centrifuged again at 10,000 rcf for 10 minutes. Size Exclusion Chromatography and SAXS Analysis: Approximately 65 μl of the supernatant were loaded onto a Superose 6 Increase 10/300 column (GE Healthcare), equilibrated in DPBS buffer (137 mM NaCl, 2.7 mM KCl, 10 mM phosphate buffer, pH 7.4, 0.9 mM CaCl2, 0.5 mM MgCl2). The flow rate was set at 0.5 ml/min. SAXS frames corresponding to the monomeric 24mer fraction of apoferritin (elution volume range: 14.5–14.75 ml) with a constant Rg value were selected for further analysis.
experiment_descriptionSynchrotron SAXS data from solutions of horse spleen apoferritin in 137 mM NaCl, 2.7 mM KCl, 10 mM phosphate buffer, 0.9 mM CaCl2, 0.5 mM MgCl2, pH 7.4 were collected on the BL19U2 beam line at the Shanghai Synchrotron Radiation Facility (SSRF; Shanghai, China) using a Pilatus 1M detector at a sample-detector distance of 2.7 m and at a wavelength of λ = 0.1033 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 65.00 μl sample at 22.3 mg/ml was injected at a 0.50 ml/min flow rate onto a GE Superose 6 Increase 10/300 column at 20°C. 40 successive 1 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
experimental_mw464.48
experimental_mw_errornull
guinier_i0_mwnull
guinier_i0_mw_errornull
porod_mw537.91
porod_mw_errornull
pddf_i00.2464
pddf_i0_errornull
guinier_i00.248256
guinier_i0_errornull
pddf_rg5.24
pddf_rg_errornull
guinier_rg5.385
guinier_rg_error0.056
pddf_dmax13.5
pddf_dmax_errornull
porod_volume650.81
porod_volume_errornull
estimated_volumenull
estimated_volume_errornull
guinier_point_first4
guinier_point_last52
pddf_point_firstnull
pddf_point_lastnull
i0_calibration_standard_datanull
intensities_log_log_plotSASDWV6_datloglog_img.png
symmetrynull
last_modified2026-02-04T12:11:49.985403+01:00
bragg_peak[]
manifest.json:34 个字段值
字段路径原始值
codeSASDWV6
statussuccess
started_at2026-08-11T15:17:00.539149+00:00
finished_at2026-08-11T15:17:09.442710+00:00
source_last_modified2026-02-04T12:11:49.985403+01:00
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查看完整 summary.json 原文
{
  "code": "SASDWV6",
  "status": "Published",
  "type_of_curve": "SEC-SAS",
  "angular_unit": "1/A",
  "project": {
    "title": "Structural insights into the nature of static and dynamic apoferritin dimers",
    "publication": null,
    "status": "released",
    "submitted_date": "2025-01-28",
    "released_date": "2026-01-28"
  },
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  "intensities_data": "https://www.sasbdb.org/media/intensities_files/SASDWV6.dat",
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          "sequence": "SSQIRQNYSTEVEAAVNRLVNLYLRASYTYLSLGFYFDRDDVALEGVCHFFRELAEEKREGAERLLKMQNQRGGRALFQDLQKPSQDEWGTTLDAMKAAIVLEKSLNQALLDLHALGSAQADPHLCDFLESHFLDEEVKLIKKMGDHLTNIQRLVGSQAGLGEYLFERLTLKHD",
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          "oligomerization": "24-mer",
          "molecular_type": "protein",
          "uniprot_sequence": "MSSQIRQNYSTEVEAAVNRLVNLYLRASYTYLSLGFYFDRDDVALEGVCHFFRELAEEKR\nEGAERLLKMQNQRGGRALFQDLQKPSQDEWGTTLDAMKAAIVLEKSLNQALLDLHALGSA\nQADPHLCDFLESHFLDEEVKLIKKMGDHLTNIQRLVGSQAGLGEYLFERLTLKHD",
          "mw": 19.846,
          "total_mw": 476.304,
          "number_molecules": 24,
          "complex_state": false,
          "deuteration": null,
          "molecule_source": "biological",
          "molecule_description": "Monomer of horse spleen apoferritin"
        }
      ],
      "buffer": {
        "name": "137 mM NaCl, 2.7 mM KCl, 10 mM phosphate buffer, 0.9 mM CaCl2, 0.5 mM MgCl2",
        "concentration_unit": null,
        "comment": null,
        "additive": null,
        "concentration": null,
        "pka": null,
        "ph": 7.4,
        "deuteration": null
      },
      "purity_method": null,
      "name": "SEC-SAXS data for the monomeric (24mer) fraction of horse spleen apoferritin",
      "ext_coefficient": null,
      "contrast": null,
      "specific_vol": null,
      "dry_vol": null,
      "absorbption": null,
      "deuteration": null,
      "mixture": null
    },
    "contributor": [
      {
        "affiliation": [
          {
            "short_name": null,
            "address": null,
            "full_name": "University of Groningen",
            "webpage": null
          }
        ],
        "contributor_name": "Aleksei",
        "contributor_surname": "Tsarenko",
        "orcid": "https://orcid.org/0000-0002-4221-3317"
      }
    ],
    "concentration_method": null,
    "concentration_unit": null,
    "date": "2024-05-24",
    "storage_temperature": 4.0,
    "cell_temperature": 20.0,
    "exposure_time": 1.0,
    "number_of_frames": 40,
    "wavelength": 0.1033,
    "sample_detector_distance": 2.696,
    "concentration_min": null,
    "concentration_max": 22.3,
    "sample_volume": 65.0,
    "flow_rate": 0.5,
    "s_min": 0.058,
    "s_max": 4.068,
    "total_exposure_time": null,
    "seccolumn": 5
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  "fits": [
    {
      "models": [
        {
          "model_plot": "https://www.sasbdb.org/media/pdb_file/images/SASDWV6_fit1_model1_img.png",
          "software": "Chimera",
          "pdb_link": [
            {
              "pdb_code": "2w0o",
              "ext_code": "2W0O",
              "ext_type": "pdb",
              "difference_with_model": "identical"
            }
          ],
          "model_title": null,
          "type_of_model": "atomic",
          "software_version": "1.14",
          "model_data": "https://www.sasbdb.org/media/pdb_file/SASDWV6_fit1_model1.pdb",
          "model_mw": 464.5,
          "bead_radius": null,
          "log": null,
          "symmetry": null,
          "comment": null,
          "user": 1173
        }
      ],
      "fit_unit": "1/A",
      "fit_plot": "https://www.sasbdb.org/media/fitting_files/scattering_plots/SASDWV6_fit1_fixed_fit_img.png",
      "software": "CRYSOL",
      "chi_square_value": 14.583,
      "p_value": 0.0,
      "fit_residual_plot": "SASDWV6_fit1_fitresiduals_img.png",
      "fit_data": "https://www.sasbdb.org/media/fitting_files/SASDWV6_fit1.fit",
      "fit_log": "https://www.sasbdb.org/media/fitting_files/log_files/24-mer_woH2O03_UzFcVcG.log",
      "software_version": "3.0",
      "description": ""
    }
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  "pddf_software": "ATSAS GNOM",
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  "i0_calibration_standard": null,
  "description": "The preparation and analysis of horse spleen apoferritin were conducted to isolate its monomeric (24mer) and dimeric (2 x 24mer) forms and enable detailed structural characterization.\r\n     Sample Preparation:\r\nHorse spleen apoferritin (purchased from Sigma-Aldrich, Merck KGaA, Germany), supplied with 50% v/v glycerol, was dialyzed overnight against 200 mM sodium acetate (pH 5.0). The dialyzed sample was then heated at 50°C for 5 hours, followed by centrifugation at 20,000 rcf for 15 minutes. The resulting supernatant was injected into a Superose 6 column (24 ml).\r\n     Fractionation and Concentration:\r\nFractions corresponding to apoferritin 24mer monomers were pooled and neutralized by adding an appropriate volume of 1M Tris (pH 8.0). The sample was concentrated to a final concentration of 22 mg/ml using a 100 kDa centrifuge spin filter and centrifuged again at 10,000 rcf for 10 minutes.\r\n     Size Exclusion Chromatography and SAXS Analysis:\r\nApproximately 65 μl of the supernatant were loaded onto a Superose 6 Increase 10/300 column (GE Healthcare), equilibrated in DPBS buffer (137 mM NaCl, 2.7 mM KCl, 10 mM phosphate buffer, pH 7.4, 0.9 mM CaCl2, 0.5 mM MgCl2). The flow rate was set at 0.5 ml/min. SAXS frames corresponding to the monomeric 24mer fraction of apoferritin (elution volume range: 14.5–14.75 ml) with a constant Rg value were selected for further analysis.",
  "experiment_description": "Synchrotron SAXS data from solutions of horse spleen apoferritin in 137 mM NaCl, 2.7 mM KCl, 10 mM phosphate buffer, 0.9 mM CaCl2, 0.5 mM MgCl2, pH 7.4 were collected on the BL19U2 beam line at the Shanghai Synchrotron Radiation Facility (SSRF; Shanghai, China) using a Pilatus 1M detector at a sample-detector distance of 2.7 m and at a wavelength of λ = 0.1033 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 65.00 μl sample at 22.3 mg/ml was injected at a 0.50 ml/min flow rate onto a GE Superose 6 Increase 10/300 column at 20°C. 40 successive 1 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_unit": "1/cm",
  "experimental_mw": 464.48,
  "experimental_mw_error": null,
  "guinier_i0_mw": null,
  "guinier_i0_mw_error": null,
  "porod_mw": 537.91,
  "porod_mw_error": null,
  "pddf_i0": 0.2464,
  "pddf_i0_error": null,
  "guinier_i0": 0.248256,
  "guinier_i0_error": null,
  "pddf_rg": 5.24,
  "pddf_rg_error": null,
  "guinier_rg": 5.385,
  "guinier_rg_error": 0.056,
  "pddf_dmax": 13.5,
  "pddf_dmax_error": null,
  "porod_volume": 650.81,
  "porod_volume_error": null,
  "estimated_volume": null,
  "estimated_volume_error": null,
  "guinier_point_first": 4,
  "guinier_point_last": 52,
  "pddf_point_first": null,
  "pddf_point_last": null,
  "i0_calibration_standard_data": null,
  "intensities_log_log_plot": "SASDWV6_datloglog_img.png",
  "symmetry": null,
  "last_modified": "2026-02-04T12:11:49.985403+01:00",
  "bragg_peak": []
}
查看完整 manifest.json 原文
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  "finished_at": "2026-08-11T15:17:09.442710+00:00",
  "source_last_modified": "2026-02-04T12:11:49.985403+01:00",
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