RRC ID 38577
Author Sun F, Mikuni S, Kinjo M.
Title Monitoring the caspase cascade in single apoptotic cells using a three-color fluorescent protein substrate.
Journal Biochem Biophys Res Commun
Abstract Fluorescence cross-correlation spectroscopy (FCCS) reveals information about the spatiotemporal coincidence of two spectrally well-defined fluorescent molecules in a small observation area at the level of single-molecule sensitivity. To simultaneously evaluate the activities of caspase-3 and caspase-9, we constructed a chimeral protein that consisted of tandemly fused enhanced cyan fluorescent protein (ECFP), monomeric red fluorescent protein (mCherry) and monomeric yellow fluorescent protein (Venus). In HeLa cell lysates, a combination of tumor necrosis factor-α (TNF-α)- and cycloheximide (CHX-)-induced apoptosis was monitored. In this, decreases of cross-correlation amplitudes were observed between ECFP and mCherry and between mCherry and Venus. Moreover, time-dependent monitoring of single cells revealed decreases in the cross-correlation amplitudes between ECFP and mCherry and between mCherry and Venus before morphologic changes were observed by laser scanning fluorescence microscopy (LSM). Thus, our method could predict the fate of the cell in the early apoptotic stage.
Volume 404(2)
Pages 706-10
Published 2011-1-14
DOI 10.1016/j.bbrc.2010.12.047
PII S0006-291X(10)02285-0
PMID 21156159
MeSH Apoptosis* Bacterial Proteins / analysis Bacterial Proteins / genetics Caspase 3 / analysis* Caspase 3 / biosynthesis Caspase 9 / analysis* Caspase 9 / biosynthesis Fluorescent Dyes / analysis Green Fluorescent Proteins / analysis Green Fluorescent Proteins / genetics HeLa Cells Humans Luminescent Proteins / analysis Luminescent Proteins / genetics Recombinant Fusion Proteins / analysis Recombinant Fusion Proteins / genetics Spectrometry, Fluorescence / methods* Tumor Necrosis Factor-alpha / pharmacology
IF 2.985
Times Cited 4
WOS Category BIOPHYSICS BIOCHEMISTRY & MOLECULAR BIOLOGY
Resource
Human and Animal Cells