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dc.contributor.author Le, Phuong -
dc.contributor.author Lim, Sung Jun -
dc.contributor.author Baculis, Brian C. -
dc.contributor.author Chung, Hee Jung -
dc.contributor.author Kilian, Kristopher A. -
dc.contributor.author Smith, Andrew M. -
dc.date.accessioned 2019-03-18T00:47:54Z -
dc.date.available 2019-03-18T00:47:54Z -
dc.date.created 2019-03-15 -
dc.date.issued 2019-02 -
dc.identifier.issn 2041-1723 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/9637 -
dc.description.abstract The distribution of single-cell properties across a population of cells can be measured using diverse tools, but no technology directly quantifies the biochemical stimulation events regulating these properties. Here we report digital counting of growth factors in single cells using fluorescent quantum dots and calibrated three-dimensional deconvolution microscopy (QDC-3DM) to reveal physiologically relevant cell stimulation distributions. We calibrate the fluorescence intensities of individual compact quantum dots labeled with epidermal growth factor (EGF) and demonstrate the necessity of near-infrared emission to overcome intrinsic cellular autofluoresence at the single-molecule level. When applied to human triple-negative breast cancer cells, we observe proportionality between stimulation and both receptor internalization and inhibitor response, reflecting stimulation heterogeneity contributions to intrinsic variability. We anticipate that QDC-3DM can be applied to analyze any peptidic ligand to reveal single-cell correlations between external stimulation and phenotypic variability, cell fate, and drug response. © 2019, The Author(s). -
dc.language English -
dc.publisher Nature Publishing Group -
dc.title Counting growth factors in single cells with infrared quantum dots to measure discrete stimulation distributions -
dc.type Article -
dc.identifier.doi 10.1038/s41467-019-08754-5 -
dc.identifier.scopusid 2-s2.0-85062015994 -
dc.identifier.bibliographicCitation Nature Communications, v.10, no.1 -
dc.description.isOpenAccess TRUE -
dc.subject.keywordPlus FACTOR RECEPTOR -
dc.subject.keywordPlus GENE-EXPRESSION -
dc.subject.keywordPlus EGFR -
dc.subject.keywordPlus MOLECULE -
dc.subject.keywordPlus ORIGINS -
dc.subject.keywordPlus TUMOR -
dc.subject.keywordPlus VARIABILITY -
dc.subject.keywordPlus ACTIVATION -
dc.subject.keywordPlus MECHANISMS -
dc.subject.keywordPlus THERAPIES -
dc.citation.number 1 -
dc.citation.title Nature Communications -
dc.citation.volume 10 -
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Division of Nanotechnology 1. Journal Articles

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