Multi-Color Enhanced Fluorescence Imaging of a Breast Cancer Cell with A Hole-Arrayed Plasmonic Chip.
Makiko YoshidaHinako ChidaFukiko KimuraShohei YamamuraKeiko TawaPublished in: Micromachines (2020)
Breast cancer cells of MDA-MB-231 express various types of membrane proteins in the cell membrane. In this study, two types of membrane proteins in MDA-MB-231 cells were observed using a plasmonic chip with an epifluorescence microscope. The targeted membrane proteins were epithelial cell adhesion molecules (EpCAMs) and epidermal growth factor receptor (EGFR), and Alexa®488-EGFR antibody and allophycocyanin (APC)-labeled EpCAM antibody were applied to the fluorescent detection. The plasmonic chip used in this study is composed of a two-dimensional hole-array structure, which is expected to enhance the fluorescence at different resonance wavelengths due to two kinds of grating pitches in a square side and a diagonal direction. As a result of multi-color imaging, the enhancement factor of Alexa®488-EGFR and APC-EpCAM was 13 ± 2 and 12 ± 2 times greater on the plasmonic chip, respectively. The excited wavelength or emission wavelength of each fluorescent agent is due to consistency with plasmon resonance wavelength in the hole-arrayed chip. The multi-color fluorescence images of breast cancer cells were improved by the hole-arrayed plasmonic chip.
Keyphrases
- energy transfer
- epidermal growth factor receptor
- circulating tumor cells
- breast cancer cells
- quantum dots
- high throughput
- cell adhesion
- tyrosine kinase
- single molecule
- label free
- small cell lung cancer
- fluorescence imaging
- advanced non small cell lung cancer
- perovskite solar cells
- single cell
- induced apoptosis
- high resolution
- solar cells
- living cells
- stem cells
- deep learning
- oxidative stress
- mesenchymal stem cells
- cell therapy
- machine learning
- convolutional neural network
- mass spectrometry
- bone marrow
- endoplasmic reticulum stress
- high density
- cell death