<?xml version="1.0" encoding="UTF-8"?>

<?xml-stylesheet type="text/xsl" href="/static/oaitohtml.xsl"?>

<!--
<?xml-stylesheet type="text/xsl" href="/oaitohtml.xsl"?>
-->

<OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
    <responseDate>2026-10-14T23:06:46Z</responseDate>
    <request verb="GetRecord" metadataPrefix="oai_dc" identifier="10.57760/sciencedb.12428" >https://www.scidb.cn/oai</request>
<GetRecord>
    <record>
    <header >
    <identifier>10.57760/sciencedb.12428</identifier>
    <datestamp>2024-09-25T17:13:41Z</datestamp>
</header>
    <metadata>
        
<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:date>2024-09-25</dc:date>
  <dc:title>A dataset of Zr-NMOF Tagged with Heterobifunctionalized Aptamers for Highly Sensitive, Multiplexed and Rapid Imaging Mass Cytometry</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.12428</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Imaging&amp;nbsp;mass cytometry (IMC) permits high-dimensional single-cell spatial proteomics by harnessing mass tags to replace conventional fluorescence tags. However, the current IMC technique commonly adopts metal-chelated polymer (MCP) tags, which are limited in sensitivity, multiplicity and data acquisition speed. Here, we demonstrate&amp;nbsp;nanometal-organic framework (NMOF) tags, which could&amp;nbsp;concurrently augment IMC&amp;rsquo;s sensitivity, multiplicity and acquisition speed. We designed and synthesized&amp;nbsp;uniform-sized Zr-NMOFs (~&amp;nbsp;31 nm, PDI&amp;nbsp;&amp;lt;&amp;nbsp;0.1), and then functionalized them&amp;nbsp;with&amp;nbsp;heterobifunctionalized aptamers&amp;nbsp;containing&amp;nbsp;phosphate groups&amp;nbsp;and fluorescent moieties to generate Zr-NMOF_Aptamer probe. Such&amp;nbsp;functionalization enabled&amp;nbsp;direct ligand exchange with zirconium ions&amp;nbsp;on Zr-NMOFs, thus allowing for concurrent fluorescence and mass signal acquisitions.&amp;nbsp;The fluorescent signal enabled large-scale rapid imaging to quickly locate region-of-interest, therefore significantly&amp;nbsp;reducing IMC's blind scanning time and compensating for IMC&amp;rsquo;s lower resolution.&amp;nbsp;Meanwhile, the Zr-NMOF_Aptamer&amp;nbsp;probe exhibited specific molecular recognition and a fourfold enhancement in signal amplification over&amp;nbsp;the commercial MCP probe.&amp;nbsp;Additionally, we showed&amp;nbsp;that Zr-NMOF_Aptamer&amp;nbsp;probes were compatible with commercial MCP probes&amp;nbsp;for high-multiplex co-staining in IMC analysis. Zr-NMOF_Aptamer&amp;nbsp;probe represents a promising development of next-generation molecular probes for spatial proteomics with IMC.</dc:description>
  <dc:subject>IMC; NMOF; probes</dc:subject>
  <dc:creator>Kevin Bao</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
</oai_dc:dc>

    </metadata>
</record>
</GetRecord>
</OAI-PMH>