Spectral imaging and linear un‐mixing enables improved FRET efficiency with a novel GFP2–YFP FRET pair
- 16 October 2002
- journal article
- Published by Wiley in FEBS Letters
- Vol. 531 (2) , 245-249
- https://doi.org/10.1016/s0014-5793(02)03508-1
Abstract
Read the full review for this F1000Prime recommended article: Spectral imaging and linear un-mixing enables improved FRET efficiency with a novel GFP2-YFP FRET pair.Keywords
This publication has 16 references indexed in Scilit:
- Fluorescent indicators for imaging protein phosphorylation in single living cellsNature Biotechnology, 2002
- A variant of yellow fluorescent protein with fast and efficient maturation for cell-biological applicationsNature Biotechnology, 2002
- Resolution of multiple green fluorescent protein color variants and dyes using two-photon microscopy and imaging spectroscopyJournal of Biomedical Optics, 2001
- Systematic subcellular localization of novel proteins identified by large‐scale cDNA sequencingEMBO Reports, 2000
- Using GFP in FRET-based applicationsTrends in Cell Biology, 1999
- Bcl-2 and Bax interactions in mitochondria probed with green fluorescent protein and fluorescence resonance energy transferNature Biotechnology, 1998
- Quantitative Fluorescence Resonance Energy Transfer Measurements Using Fluorescence MicroscopyBiophysical Journal, 1998
- In vivo activation of recombinant cAPK catalytic subunit active site mutants by coexpression of the wild‐type enzyme, evidence for intermolecular cotranslational phosphorylationFEBS Letters, 1996
- Engineering green fluorescent protein for improved brightness, longer wavelengths and fluorescence resonance energy transferCurrent Biology, 1996
- Oligomerization of epidermal growth factor receptors on A431 cells studied by time-resolved fluorescence imaging microscopy. A stereochemical model for tyrosine kinase receptor activation.The Journal of cell biology, 1995