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Open AccessArticle

Dual-Color Fluorescence Imaging of EpCAM and EGFR in Breast Cancer Cells with a Bull’s Eye-Type Plasmonic Chip

1
School of Science and Technology, Kwansei Gakuin University, 2-1 Gakuen, Sanda, Hyōgo 669-1337, Japan
2
Health Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), 2217-14, Hayashi-cho, Takamatsu, Kagawa 761-0395, Japan
*
Author to whom correspondence should be addressed.
Sensors 2017, 17(12), 2942; https://doi.org/10.3390/s17122942
Received: 6 October 2017 / Revised: 11 December 2017 / Accepted: 15 December 2017 / Published: 19 December 2017
Surface plasmon field-enhanced fluorescence microscopic observation of a live breast cancer cell was performed with a plasmonic chip. Two cell lines, MDA-MB-231 and Michigan Cancer Foundation-7 (MCF-7), were selected as breast cancer cells, with two kinds of membrane protein, epithelial cell adhesion molecule (EpCAM) and epidermal growth factor receptor (EGFR), observed in both cells. The membrane proteins are surface markers used to differentiate and classify breast cancer cells. EGFR and EpCAM were detected with Alexa Fluor® 488-labeled anti-EGFR antibody (488-EGFR) and allophycocyanin (APC)-labeled anti-EpCAM antibody (APC-EpCAM), respectively. In MDA-MB231 cells, three-fold plus or minus one and seven-fold plus or minus two brighter fluorescence of 488-EGFR were observed on the 480-nm pitch and the 400-nm pitch compared with that on a glass slide. Results show the 400-nm pitch is useful. Dual-color fluorescence of 488-EGFR and APC-EpCAM in MDA-MB231 was clearly observed with seven-fold plus or minus two and nine-fold plus or minus three, respectively, on the 400-nm pitch pattern of a plasmonic chip. Therefore, the 400-nm pitch contributed to the dual-color fluorescence enhancement for these wavelengths. An optimal grating pitch of a plasmonic chip improved a fluorescence image of membrane proteins with the help of the surface plasmon-enhanced field. View Full-Text
Keywords: surface plasmon; fluorescence microscopic observation; breast cancer cell; membrane protein surface plasmon; fluorescence microscopic observation; breast cancer cell; membrane protein
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MDPI and ACS Style

Izumi, S.; Yamamura, S.; Hayashi, N.; Toma, M.; Tawa, K. Dual-Color Fluorescence Imaging of EpCAM and EGFR in Breast Cancer Cells with a Bull’s Eye-Type Plasmonic Chip. Sensors 2017, 17, 2942. https://doi.org/10.3390/s17122942

AMA Style

Izumi S, Yamamura S, Hayashi N, Toma M, Tawa K. Dual-Color Fluorescence Imaging of EpCAM and EGFR in Breast Cancer Cells with a Bull’s Eye-Type Plasmonic Chip. Sensors. 2017; 17(12):2942. https://doi.org/10.3390/s17122942

Chicago/Turabian Style

Izumi, Shota; Yamamura, Shohei; Hayashi, Naoko; Toma, Mana; Tawa, Keiko. 2017. "Dual-Color Fluorescence Imaging of EpCAM and EGFR in Breast Cancer Cells with a Bull’s Eye-Type Plasmonic Chip" Sensors 17, no. 12: 2942. https://doi.org/10.3390/s17122942

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