<entry xmlns="http://pdbe.org/empiar" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="https://ftp.ebi.ac.uk/pub/databases/emtest/empiar/schema/empiar.xsd" accessionCode="EMPIAR-12794" schemaVersion="0.65" public="true">
    <admin>
        <currentStatus>REL</currentStatus>
        <keyDates>
            <depositionDate>2025-01-27</depositionDate>
            <releaseDate>2025-07-25</releaseDate>
            <updateDate>2025-07-25</updateDate>
        </keyDates>
        <title>Cryo-electron tomography on synaptic vesicles isolated from mouse brain (part 1)</title>
        <correspondingAuthor private="true">
            <authorORCID>0000-0003-3550-6274</authorORCID>
            <firstName>Mikhail</firstName>
            <lastName>Kudryashev</lastName>
            <organization type="academic">Max Delbrück Center for Molecular Medicine</organization>
            <townOrCity>Berlin</townOrCity>
            <country>Germany</country>
            <postOrZipCode>13125</postOrZipCode>
        </correspondingAuthor>
        <principalInvestigator private="true">
            <authorORCID>0000-0003-3550-6274</authorORCID>
            <firstName>Mikhail</firstName>
            <lastName>Kudryashev</lastName>
            <organization type="academic">Max Delbrück Center for Molecular Medicine</organization>
            <townOrCity>Berlin</townOrCity>
            <country>Germany</country>
            <postOrZipCode>13125</postOrZipCode>
        </principalInvestigator>
        <authorsList>
            <author authorORCID="0009-0004-7176-8444">Kravcenko U</author>
            <author authorORCID="0009-0000-7220-406X">Ruwolt M</author>
            <author authorORCID="0000-0003-4243-4088">Kroll J</author>
            <author authorORCID="0000-0002-8729-9281">Yushkevich A</author>
            <author>Zenkner M</author>
            <author authorORCID="0009-0007-0524-6885">Ruta J</author>
            <author>Lotfy R</author>
            <author authorORCID="0000-0001-8072-1630">Wanker EE</author>
            <author authorORCID="0000-0002-3905-2444">Rosenmund C</author>
            <author>Liu F</author>
            <author authorORCID="0000-0003-3550-6274">Kudryashev M</author>
        </authorsList>
        <grantSupport>
            <grantReference>
                <fundingBody>German Research Foundation (DFG)</fundingBody>
                <code>KU3222/3-1</code>
                <country>Germany</country>
            </grantReference>
            <grantReference>
                <fundingBody>German Research Foundation (DFG)</fundingBody>
                <code>458275811</code>
                <country>Germany</country>
            </grantReference>
            <grantReference>
                <fundingBody>German Research Foundation (DFG)</fundingBody>
                <code>436260754</code>
                <country>Germany</country>
            </grantReference>
            <grantReference>
                <fundingBody>European Research Council (ERC)</fundingBody>
                <code>ERC-STG No. 949184</code>
                <country>Germany</country>
            </grantReference>
        </grantSupport>
        <datasetSize units="TB">1.4</datasetSize>
        <entryDOI>10.6019/EMPIAR-12794</entryDOI>
        <experimentType>EMDB</experimentType>
        <scale>molecule</scale>
    </admin>
    <crossReferences>
        <relatedEMDBEntries>
            <emdbEntry>EMD-18556</emdbEntry>
            <emdbEntry>EMD-18557</emdbEntry>
            <emdbEntry>EMD-18572</emdbEntry>
            <emdbEntry>EMD-18568</emdbEntry>
            <emdbEntry>EMD-18578</emdbEntry>
        </relatedEMDBEntries>
        <citationList>
            <universalCitation>
                <journalCitation published="true" preprint="false">
                    <author authorORCID="0009-0004-7176-8444" order="1">Kravcenko U</author>
                    <author authorORCID="0000-0003-3550-6274" order="2">Kudryashev M</author>
                    <title>Molecular architecture of synaptic vesicles</title>
                    <journal>Proceedings of the National Academy of Sciences</journal>
                    <journalAbbreviation>PNAS</journalAbbreviation>
                    <country>United States</country>
                    <issue>49</issue>
                    <volume>121</volume>
                    <year>2024</year>
                    <language>English</language>
                    <externalReferences type="doi">10.1073/pnas.2407375121</externalReferences>
                    <externalReferences type="pubmed">39602275</externalReferences>
                </journalCitation>
            </universalCitation>
        </citationList>
    </crossReferences>
    <imageSet>
        <name>Source unaligned micrographs (.tif) of synaptic vesicles isolated from mouse brain (part I)</name>
        <directory>/data/frames_1</directory>
        <category>micrographs - multiframe</category>
        <headerFormat>TIFF</headerFormat>
        <dataFormat>TIFF</dataFormat>
        <numImagesOrTiltSeries>48</numImagesOrTiltSeries>
        <framesPerImage>10</framesPerImage>
        <voxelType>UNSIGNED BYTE</voxelType>
        <dimensions>
            <imageWidth>11520</imageWidth>
            <pixelWidth>0.84</pixelWidth>
            <imageHeight>8184</imageHeight>
            <pixelHeight>0.84</pixelHeight>
        </dimensions>
        <details>The naming correspondence between raw micrographs and tilt series/tomograms can be found in frames2tomos.txt.
The respective gain-reference file is SuperCDSRef_A_000_0.0.dm4
For this dataset raw micrographs were collected in 10 frames with a total dose per tilt view of 4.1391 e−/Å2 and the total dose distributed equally among all tilt images.
See top-level README.txt for contents location details.</details>
        <segmentationList/>
        <micrographsFilePattern></micrographsFilePattern>
        <pickedParticlesFilePattern></pickedParticlesFilePattern>
        <pickedParticlesDirectory></pickedParticlesDirectory>
    </imageSet>
    <imageSet>
        <name>Source unaligned micrographs (.tif) of synaptic vesicles isolated from mouse brain (part II)</name>
        <directory>/data/frames_2</directory>
        <category>micrographs - multiframe</category>
        <headerFormat>TIFF</headerFormat>
        <dataFormat>TIFF</dataFormat>
        <numImagesOrTiltSeries>64</numImagesOrTiltSeries>
        <framesPerImage>10</framesPerImage>
        <voxelType>UNSIGNED BYTE</voxelType>
        <dimensions>
            <imageWidth>11520</imageWidth>
            <pixelWidth>0.84</pixelWidth>
            <imageHeight>8184</imageHeight>
            <pixelHeight>0.84</pixelHeight>
        </dimensions>
        <details>The naming correspondence between raw micrographs and tilt series/tomograms can be found in frames2tomos.txt.
The respective gain-reference file is SuperCDSRef_ts_051_000_-0.0.dm4
For this dataset raw micrographs were collected using high-dose zero-tilt scheme. Thus, a zero-tilt micrographs were collected in 75 frames with a total dose per image of 31.077 e−/Å2 and other tilt micrographs were collected in 10 frames with a total dose per image of 4.1391 e−/Å2.
See top-level README.txt for contents location details.</details>
        <segmentationList/>
        <micrographsFilePattern></micrographsFilePattern>
        <pickedParticlesFilePattern></pickedParticlesFilePattern>
        <pickedParticlesDirectory></pickedParticlesDirectory>
    </imageSet>
    <imageSet>
        <name>Unaligned unbinned tilt stacks (.st) with metadata (.xf, .tlt, .defocus) of synaptic vesicles isolated from mouse brain</name>
        <directory>/data/Stacks</directory>
        <category>tilt series</category>
        <headerFormat>MRC</headerFormat>
        <dataFormat>MRC</dataFormat>
        <numImagesOrTiltSeries>99</numImagesOrTiltSeries>
        <framesPerImage>10</framesPerImage>
        <voxelType>32 BIT FLOAT</voxelType>
        <dimensions>
            <imageWidth>11520</imageWidth>
            <pixelWidth>0.84</pixelWidth>
            <imageHeight>8184</imageHeight>
            <pixelHeight>0.84</pixelHeight>
        </dimensions>
        <details>The metadata files could be used to align tilt stacks (.tlt and .xf), correct CTF (.defocus) and perform 3D reconstruction (.tlt), e.g. using IMOD.</details>
        <segmentationList/>
        <micrographsFilePattern></micrographsFilePattern>
        <pickedParticlesFilePattern></pickedParticlesFilePattern>
        <pickedParticlesDirectory></pickedParticlesDirectory>
    </imageSet>
    <imageSet>
        <name>CTF-corrected binned tomograms (.rec) of synaptic vesicles isolated from mouse brain</name>
        <directory>/data/tomograms</directory>
        <category>reconstructed volumes</category>
        <headerFormat>MRC</headerFormat>
        <dataFormat>MRC</dataFormat>
        <numImagesOrTiltSeries>99</numImagesOrTiltSeries>
        <framesPerImage>10</framesPerImage>
        <voxelType>32 BIT FLOAT</voxelType>
        <dimensions>
            <imageWidth>512</imageWidth>
            <pixelWidth>13.44</pixelWidth>
            <imageHeight>720</imageHeight>
            <pixelHeight>13.44</pixelHeight>
        </dimensions>
        <details>Particle coordinates and orientations could be found in the subfolder "/data/particle_tables/" of this deposition.
For additional info see file prtcls_description_dataset_1.txt</details>
        <segmentationList/>
        <micrographsFilePattern></micrographsFilePattern>
        <pickedParticlesFilePattern></pickedParticlesFilePattern>
        <pickedParticlesDirectory></pickedParticlesDirectory>
    </imageSet>
</entry>
