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<identifier>oai:icatplus.esrf.fr:inv/2116854002</identifier>
<datestamp>2025-05-30T06:00:17.281Z</datestamp>
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<identifier identifierType="DOI">10.15151/ESRF-ES-2116854002</identifier>
<creators>
<creator>
<creatorName nameType="Personal">Anne-Claire DHAUSSY</creatorName>
<givenName>Anne-Claire</givenName>
<familyName>Dhaussy</familyName>
</creator>
<creator>
<creatorName nameType="Personal">Anne-Claire DHAUSSY</creatorName>
<givenName>Anne-Claire</givenName>
<familyName>Dhaussy</familyName>
</creator>
<creator>
<creatorName nameType="Personal">Mohamed MEZOUAR</creatorName>
<givenName>Mohamed</givenName>
<familyName>Mezouar</familyName>
<nameIdentifier nameIdentifierScheme="ORCID">0000-0001-5336-544X</nameIdentifier>
</creator>
<creator>
<creatorName nameType="Personal">Nicolas COQUELLE</creatorName>
<givenName>Nicolas</givenName>
<familyName>Coquelle</familyName>
</creator>
<creator>
<creatorName nameType="Personal">Nicolas COQUELLE</creatorName>
<givenName>Nicolas</givenName>
<familyName>Coquelle</familyName>
</creator>
<creator>
<creatorName nameType="Personal">Max GERIN</creatorName>
<givenName>Max</givenName>
<familyName>Gerin</familyName>
</creator>
<creator>
<creatorName nameType="Personal">Eric GIRARD</creatorName>
<givenName>Eric</givenName>
<familyName>Girard</familyName>
<nameIdentifier nameIdentifierScheme="ORCID">0000-0002-5758-6095</nameIdentifier>
</creator>
<creator>
<creatorName nameType="Personal">Eric GIRARD</creatorName>
<givenName>Eric</givenName>
<familyName>Girard</familyName>
<nameIdentifier nameIdentifierScheme="ORCID">0000-0002-5758-6095</nameIdentifier>
</creator>
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<titles>
<title>Evaluating serail crystallography approaches for diamond anvil cell data collection.</title>
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<publisher>Example Institute</publisher>
<publicationYear>2028</publicationYear>
<resourceType resourceTypeGeneral="Collection">Data from large facility measurement</resourceType>
<dates>
<date dateType="Collected">2025-05-27T06:00:00Z/2025-05-30T06:00:00Z</date>
<date dateType="Accepted">2025-05-30T06:00:00Z</date>
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<rights rightsIdentifier="CC-BY-4.0" rightsURI="https://creativecommons.org/licenses/by/4.0">CC-BY-4.0</rights>
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<description descriptionType="Abstract">High pressure macromolecular crystallography (HPMX) is an ideal technique to trap high-energy transient conformers of proteins that are essential for biological activity and/or for interaction with partners. Using a diamond anvil cell (DAC) and collecting data at room temperature (RT) ensures that the pressure/temperature of the sample environment is precisely defined and controlled. For proteins, this usually requires large enough crystals to collect a complete data set at high resolution, hopefully radiation damage free. However, growing such crystals remain a challenge. Serial crystallography offers the possibility to collect diffraction data from micron-sized crystals at RT. Indeed, only a single diffraction frame is recorded from a small single crystal, therefore spreading the required X-ray dose to reconstruct a complete dataset over a very large number of micron-sized crystals. we want to evaluate the feasibility to combine SX and DAC techniques to push forward HPMX.</description>
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