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    <admin>
        <current_status>
            <date>2026-02-25</date>
            <code>REL</code>
            <processing_site>RCSB</processing_site>
        </current_status>
        <revision_history>
            <revision version="1.0" date="2026-02-25">
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                    <metadata>
                        <revision_type>INITIAL_RELEASE</revision_type>
                        <provider>REPOSITORY</provider>
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                    <image>
                        <revision_type>INITIAL_RELEASE</revision_type>
                        <provider>REPOSITORY</provider>
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                        <revision_type>INITIAL_RELEASE</revision_type>
                        <provider>REPOSITORY</provider>
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            </revision>
        </revision_history>
        <sites>
            <deposition>RCSB</deposition>
            <last_processing>RCSB</last_processing>
        </sites>
        <key_dates>
            <deposition>2025-02-18</deposition>
            <header_release>2026-02-25</header_release>
            <map_release>2026-02-25</map_release>
            <update>2026-02-25</update>
        </key_dates>
        <grant_support>
            <grant_reference>
                <funding_body>Department of Energy (DOE, United States)</funding_body>
                <code>DE-AC02-05CH11231</code>
                <country>United States</country>
            </grant_reference>
            <grant_reference>
                <funding_body>National Institutes of Health/National Heart, Lung, and Blood Institute (NIH/NHLBI)</funding_body>
                <code>R01HL115153</code>
                <country>United States</country>
            </grant_reference>
            <grant_reference>
                <funding_body>National Institutes of Health/National Institute of General Medical Sciences (NIH/NIGMS)</funding_body>
                <code>R01GM104427</code>
                <country>United States</country>
            </grant_reference>
            <grant_reference>
                <funding_body>National Institutes of Health/National Institute of Mental Health (NIH/NIMH)</funding_body>
                <code>R01MH077303</code>
                <country>United States</country>
            </grant_reference>
            <grant_reference>
                <funding_body>National Institutes of Health/National Institute of Diabetes and Digestive and Kidney Disease (NIH/NIDDK)</funding_body>
                <code>R01DK042667</code>
                <country>United States</country>
            </grant_reference>
        </grant_support>
        <title>A 3D density map of a 2D lattice formed by octahedral DNA origami with 70% loaded ferritin, was revealed by IMOD (Tomo #3).</title>
        <authors_list>
            <author ORCID="0000-0001-6786-8873">Liu J</author>
            <author ORCID="0000-0002-8036-2321">Ren G</author>
        </authors_list>
        <keywords>Non-averaged structure, individual particle cryo-electron tomography, IPET, cryo-ET, structural flexibility, DNA origami, 2D lattice, DNA-protein lattice, DNA</keywords>
    </admin>
    <crossreferences>
        <citation_list>
            <primary_citation>
                <journal_citation published="false">
                    <author ORCID="0000-0001-6786-8873" order="1">Liu J</author>
                    <author order="2">Zhang M</author>
                    <author order="3">Wang S</author>
                    <author order="4">Hu Z</author>
                    <author order="5">Wu H</author>
                    <author order="6">Gang O</author>
                    <author ORCID="0000-0002-8036-2321" order="7">Ren G</author>
                    <title>Non-averaged 3D structure of low-ordered 2D lattice revealed by individual-particle cryo-electron tomography</title>
                    <journal_abbreviation>To Be Published</journal_abbreviation>
                    <external_references type="CSD">0353</external_references>
                </journal_citation>
            </primary_citation>
        </citation_list>
        <other_db_list>
            <db_reference>
                <db_name>EMDB</db_name>
                <accession_id>EMD-49288</accession_id>
                <content_type>associated EM volume</content_type>
            </db_reference>
        </other_db_list>
    </crossreferences>
    <sample>
        <name>2D lattice of octahedral DNA origami with 70% loaded ferritin</name>
        <supramolecule_list>
            <complex_supramolecule supramolecule_id="1">
                <name>2D lattice of octahedral DNA origami with 70% loaded ferritin</name>
                <parent>0</parent>
                <details>The octahedral DNA origami was folded by mixing 20 nM of M13mp18 scaffold DNA with 100 nM of each staple oligonucleotide in TAE buffer containing 12.5 mM MgCl2. The mixed solution was then slowly cooled down and purified. Subsequently, the octahedral DNA origami was combined with ferritin in TAE/MgCl2 buffer, and the mixed solution was slowly cooled to room temperature.</details>
                <natural_source database="NCBI">
                    <organism ncbi="32630">synthetic construct</organism>
                </natural_source>
            </complex_supramolecule>
        </supramolecule_list>
    </sample>
    <structure_determination_list>
        <structure_determination structure_determination_id="1">
            <method>tomography</method>
            <aggregation_state>twoDArray</aggregation_state>
            <specimen_preparation_list>
                <tomography_preparation preparation_id="1">
                    <buffer>
                        <ph>8.6</ph>
                        <component>
                            <concentration units="mM">40.0</concentration>
                            <name>Tris</name>
                        </component>
                        <component>
                            <concentration units="mM">20.0</concentration>
                            <name>Acetate</name>
                        </component>
                        <component>
                            <concentration units="mM">1.0</concentration>
                            <name>EDTA</name>
                        </component>
                        <component>
                            <concentration units="mM">12.5</concentration>
                            <formula>MgCl2</formula>
                            <name>Magnesium dichloride</name>
                        </component>
                    </buffer>
                    <vitrification>
                        <cryogen_name>ETHANE</cryogen_name>
                        <chamber_humidity units="percentage">90</chamber_humidity>
                        <chamber_temperature units="K">277</chamber_temperature>
                        <instrument>LEICA EM GP</instrument>
                    </vitrification>
                    <details>The octahedral DNA origami was folded by mixing 20 nM of M13mp18 scaffold DNA and 100 nM of each staple oligonucleotide in TAE buffer containing 12.5 mM MgCl2. The mixed solution was slowly cooled down and purified. The octahedral DNA origami was mixed with ferritin in TAE/MgCl2 buffer, then the mixed solution was slowly cooled to room temperature.</details>
                    <sectioning>
                        <other_sectioning>NO SECTIONING</other_sectioning>
                    </sectioning>
                </tomography_preparation>
            </specimen_preparation_list>
            <microscopy_list>
                <tomography_microscopy microscopy_id="1">
                    <microscope>ZEISS LIBRA120PLUS</microscope>
                    <illumination_mode>FLOOD BEAM</illumination_mode>
                    <imaging_mode>BRIGHT FIELD</imaging_mode>
                    <electron_source>LAB6</electron_source>
                    <acceleration_voltage units="kV">120</acceleration_voltage>
                    <nominal_cs units="mm">2.2</nominal_cs>
                    <nominal_defocus_min units="µm">7.0</nominal_defocus_min>
                    <nominal_defocus_max units="µm">7.0</nominal_defocus_max>
                    <nominal_magnification>80000.0</nominal_magnification>
                    <specimen_holder_model>GATAN 626 SINGLE TILT LIQUID NITROGEN CRYO TRANSFER HOLDER</specimen_holder_model>
                    <cooling_holder_cryogen>NITROGEN</cooling_holder_cryogen>
                    <temperature>
                        <temperature_min units="K">79.0</temperature_min>
                        <temperature_max units="K">80.0</temperature_max>
                    </temperature>
                    <alignment_procedure>
                        <basic/>
                    </alignment_procedure>
                    <image_recording_list>
                        <image_recording image_recording_id="1">
                            <film_or_detector_model>GATAN ULTRASCAN 4000 (4k x 4k)</film_or_detector_model>
                            <number_grids_imaged>1</number_grids_imaged>
                            <number_real_images>33</number_real_images>
                            <average_exposure_time units="s">1.0</average_exposure_time>
                            <average_electron_dose_per_image units="e/Å^2">2.0</average_electron_dose_per_image>
                        </image_recording>
                    </image_recording_list>
                </tomography_microscopy>
            </microscopy_list>
            <tomography_processing image_processing_id="1">
                <image_recording_id>1</image_recording_id>
                <details>The tilt series of whole micrographs were initially aligned with IMOD.</details>
                <final_reconstruction>
                    <software_list>
                        <software>
                            <name>IPET</name>
                        </software>
                    </software_list>
                    <number_images_used>33</number_images_used>
                </final_reconstruction>
                <ctf_correction>
                    <software_list>
                        <software>
                            <name>Gctf</name>
                        </software>
                        <software>
                            <name>TOMOCTF</name>
                        </software>
                    </software_list>
                    <details>The Contrast Transfer Function (CTF) was determined by Gctf and then corrected by TOMOCTF.</details>
                    <type>PHASE FLIPPING AND AMPLITUDE CORRECTION</type>
                </ctf_correction>
            </tomography_processing>
        </structure_determination>
    </structure_determination_list>
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        <file>emd_49288.map.gz</file>
        <symmetry>
            <space_group>1</space_group>
        </symmetry>
        <data_type>IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES)</data_type>
        <dimensions>
            <col>1024</col>
            <row>1024</row>
            <sec>250</sec>
        </dimensions>
        <origin>
            <col>-512</col>
            <row>-512</row>
            <sec>-125</sec>
        </origin>
        <spacing>
            <x>1024</x>
            <y>1024</y>
            <z>250</z>
        </spacing>
        <cell>
            <a units="Å">6062.08</a>
            <b units="Å">6062.08</b>
            <c units="Å">1480.0</c>
            <alpha units="deg">90.0</alpha>
            <beta units="deg">90.0</beta>
            <gamma units="deg">90.0</gamma>
        </cell>
        <axis_order>
            <fast>X</fast>
            <medium>Y</medium>
            <slow>Z</slow>
        </axis_order>
        <statistics>
            <minimum>-331.947240000000022</minimum>
            <maximum>350.984800000000007</maximum>
            <average>0.000000003730435</average>
            <std>50.041415999999998</std>
        </statistics>
        <pixel_spacing>
            <x units="Å">5.92</x>
            <y units="Å">5.92</y>
            <z units="Å">5.92</z>
        </pixel_spacing>
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            <contour primary="true">
                <source>AUTHOR</source>
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        <label>::::EMDATABANK.org::::EMD-49288::::</label>
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