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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/117548
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dc.contributor.authorDong, H.-
dc.contributor.authorYao, D.-
dc.contributor.authorZhou, Q.-
dc.contributor.authorZhang, L.-
dc.contributor.authorTian, Y.-
dc.date.issued2019-
dc.identifier.citationChemical Communications, 2019; 55(12):1730-1733-
dc.identifier.issn1359-7345-
dc.identifier.issn1364-548X-
dc.identifier.urihttp://hdl.handle.net/2440/117548-
dc.description.abstractIt is significant to in situ monitor membrane proteins at the singlecell level for understanding the cell function. Herein, an integrated platform was designed and constructed for highly efficient cell capture and in situ sensitive SERS determination of HER2 activity in cells through rational spatial organization of multi-functional cyclic RGD nanopatterns at a disordered mesoporous gold film via electrochemical activation.-
dc.description.statementofresponsibilityHui Dong, Dazhi Yao, Qi Zhou, Limin Zhang and Yang Tian-
dc.language.isoen-
dc.publisherRoyal Society of Chemistry-
dc.rightsThis journal is © The Royal Society of Chemistry 2019-
dc.source.urihttp://dx.doi.org/10.1039/c8cc09108k-
dc.subjectCell Line, Tumor-
dc.subjectHumans-
dc.subjectGold-
dc.subjectPeptides, Cyclic-
dc.subjectReceptor, erbB-2-
dc.subjectMicroscopy, Electron, Transmission-
dc.subjectMicroscopy, Fluorescence-
dc.subjectSpectrum Analysis, Raman-
dc.subjectPorosity-
dc.subjectNeoplastic Cells, Circulating-
dc.titleAn integrated platform for capture of circulating tumor cells and in situ SERS profiling of membrane proteins through rational spatial organization of multi-functional cyclic RGD nanopatterns-
dc.typeJournal article-
dc.identifier.doi10.1039/C8CC09108K-
pubs.publication-statusPublished-
dc.identifier.orcidYao, D. [0000-0002-8019-0160]-
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Chemical Engineering publications

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