- Abstract:
-
Fluorescent lifetime imaging microscopy (FLIM) has proven to be a valuable tool in beating the Rayleigh criterion for light microscopy by measuring Förster resonance energy transfer (FRET) between two fluorophores. Applying multiphoton FLIM, we previously showed in a human breast cancer cell line that recycling of a membrane receptorgreen fluorescent protein fusion is enhanced concomitantly with the formation of a receptor:protein kinase C a complex in the endosomal compartment. We have exten...
Expand abstract - Publication status:
- Published
- Publisher copy:
- 10.1117/12.817129
-
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- Journal:
- MULTIPHOTON MICROSCOPY IN THE BIOMEDICAL SCIENCES IX
- Volume:
- 7183
- Publication date:
- 2009-01-01
- DOI:
- ISSN:
-
0277-786X
- URN:
-
uuid:b403f554-710b-4e84-9348-ec8c52e0a875
- Source identifiers:
-
95003
- Local pid:
- pubs:95003
- Language:
- English
- Keywords:
- Copyright date:
- 2009
Journal article
Deep-tissue multi-photon fluorescence lifetime microscopy for intravital imaging of protein-protein interactions
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