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Title: FRET measurements between small numbers of molecules identifies subtle changes in receptor interactions
Authors: Özçelik, Serdar
Orr, Galya
Hu, Dehong
Chen, Chii-Shiarng
Reşat, Haluk
Harms, Greg S.
Opresko, Lee K.
John Wiley and Sons Inc., H. Steven
Colson, Steven D.
Keywords: FRET
Issue Date: 8-Oct-2013
Publisher: SPIE
Source: Özçelik, S., Orr, G., Hu, D., Chen, C.-S., Resat, H., Harms, G.S., Opresko, L.K., Wiley, H.S., & Colson, S.D. (June 21, 2004). FRET measurements between small numbers of molecules identifies subtle changes in receptor interactions. Proc. SPIE 5323, Multiphoton Microscopy in the Biomedical Sciences IV, 119. doi:10.1117/12.536770
Abstract: Overexpression of HER2 alters the cellular behavior of EGF receptor (EGFR) and itself,with great implications on cell fate. To understand the molecular interactions underlying these alterations, we quantified the association between the two receptors by looking at efficiency changes in fluorescence resonance energy transfer (FRET) between a small number of molecules at the membrane of living cells. Human mammary epithelial (HME) cells expressing varying degrees of HER2 were studied, to identify and compare the degree of receptors interactions as a function of HER2 overexpression. A high resolution wide-field laser microscope combined with a high sensitivity cooled CCD camera was used to capture simultaneously donor and acceptor emissions. Alternating between green and red lasers every 80 msec, donor, FRET, and acceptor images were acquired and were used to calculate FRET efficiency. Automated image analysis was developed to create FRET efficiency maps from overlapping donor, acceptor and FRET images, and derive FRET efficiency histograms to quantify receptorreceptor interactions pixel by pixel. This approach enabled us to detect subtle changes in the average distance between EGFR molecules, and between EGFR and HER2. We found pre-existing EGFR homoassociations, and EGFR-HER2 heteroassociations in cells overexpressing HER2, and identified the changes in these interactions with ligand stimulation. These observations demonstrate the power of FRET measurements between small numbers of molecules in identifying subtle changes in molecular interactions in living cell.
Appears in Collections:Chemistry / Kimya
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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