<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Zhang Y</submitter><funding>Chan Zuckerberg Biohub</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><funding>Japan Society for the Promotion of Science</funding><pubmed_abstract>Extracellular signal-regulated kinase (ERK) signaling is essential to regulated cell behaviors, including cell proliferation, differentiation, and apoptosis. The influence of cell-cell contacts on ERK signaling is central to epithelial cells, yet few studies have sought to understand the same in cancer cells, particularly with single-cell resolution. To acquire same-cell measurements of both phenotypic (cell-contact state) and targeted-protein (ERK phosphorylation) profiles, we prepend high-content, whole-cell imaging prior to end-point cellular-resolution Western blot analyses for each of hundreds of individual HeLa cancer cells cultured on that same chip, which we call &lt;i>contact&lt;/i>Blot. By indexing the phosphorylation level of ERK in each cell or cell cluster to the imaged cell-contact</pubmed_abstract><journal>Analytical chemistry</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11447967</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>&amp;lt;i&amp;gt;Contact&amp;lt;/i&amp;gt;Blot: Microfluidic Control and Measurement of the Cell-Cell Contact State to Assess Contact-Inhibited ERK Signaling.</pubmed_title><pmcid>PMC11447967</pmcid><funding_grant_id>R01CA203018</funding_grant_id><funding_grant_id>R33 CA225296</funding_grant_id><funding_grant_id>JP22H02761</funding_grant_id><funding_grant_id>JP18H02569</funding_grant_id><funding_grant_id>R01 CA203018</funding_grant_id><funding_grant_id>R33CA225296</funding_grant_id><funding_grant_id>JP15KK0297</funding_grant_id><pubmed_authors>Herr AE</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Naguro I</pubmed_authors><pubmed_authors>Ryuno H</pubmed_authors></additional><is_claimable>false</is_claimable><name>&amp;lt;i&amp;gt;Contact&amp;lt;/i&amp;gt;Blot: Microfluidic Control and Measurement of the Cell-Cell Contact State to Assess Contact-Inhibited ERK Signaling.</name><description>Extracellular signal-regulated kinase (ERK) signaling is essential to regulated cell behaviors, including cell proliferation, differentiation, and apoptosis. The influence of cell-cell contacts on ERK signaling is central to epithelial cells, yet few studies have sought to understand the same in cancer cells, particularly with single-cell resolution. To acquire same-cell measurements of both phenotypic (cell-contact state) and targeted-protein (ERK phosphorylation) profiles, we prepend high-content, whole-cell imaging prior to end-point cellular-resolution Western blot analyses for each of hundreds of individual HeLa cancer cells cultured on that same chip, which we call &lt;i>contact&lt;/i>Blot. By indexing the phosphorylation level of ERK in each cell or cell cluster to the imaged cell-contact</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Sep</publication><modification>2025-04-26T10:24:15.944Z</modification><creation>2025-04-06T13:23:04.313Z</creation></dates><accession>S-EPMC11447967</accession><cross_references><pubmed>39254112</pubmed><doi>10.1021/acs.analchem.4c02936</doi></cross_references></HashMap>