The Kahn Dynamic Proteomics project aims at monitoring the position and
amounts of endogenous proteins in individual living human cells. This is based on the
Library of Annotated
Reporter Cell-clones (LARC). Each cell-line clone contains an endogenous protein fused to yellow fluorescent protein (YFP),
expressed from its endogenous chromosomal location with its natural regulation. Labeling with YFP was done
by exon-tagging (also known as
CD-tagging), where YFP, flanked by splice signals, was delivered into the genome
using a retrovirus. YFP is then
spliced into the protein as a new exon. Protein identity was established by
sequencing the cDNA. The cell line used is the H1299 non-small lung cell carcinoma line which stably expressed
the viral receptor. This is a robust cell-line with a nicely spread cell morphology that is highly photogenic for
microscopy purposes. Several lines of evidence indicate that over 2/3 of the tagged proteins retain their proper
functionality and localization.
The amount and location of each tagged protein is monitored by means of
automated time-lapse
fluorescence microscopy in controlled CO2 and humidity conditions. Movies of the cells are automatically processed using
dedicated image analysis software. This yields quantitative traces of protein amounts and localization over time
for each individual cell in a response to the chemotheraphy drug Camptothecin (C9911 Sigma).
This site contains a database of the proteins tagged by YFP. Each protein entry
includes detailed
sequence and functional annotation, images of
protein localization,
movies and protein dynamics and links to other
databases: InterPro, GeneCards, Ensembl, Entrez, UniProt.
Sequence Analysis tools are available for up to 70 sequences provided by a user within all the cDNA sequences in
the database. The Search and Comparison of protein
dynamics are offered for all unique proteins with high-quality time-lapse fluorescence movies available in the
database.
The site is updated regularly as new clones are added to the protein library.
Supported by the Kahn Family Foundation.
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