Published January 2010 | Version Published
Journal Article Open

Dynamic Proteomics: a database for dynamics and localizations of endogenous fluorescently-tagged proteins in living human cells

Abstract

Recent advances allow tracking the levels and locations of a thousand proteins in individual living human cells over time using a library of annotated reporter cell clones (LARC). This library was created by Cohen et al. to study the proteome dynamics of a human lung carcinoma cell-line treated with an anti-cancer drug. Here, we report the Dynamic Proteomics database for the proteins studied by Cohen et al. Each cell-line clone in LARC has a protein tagged with yellow fluorescent protein, expressed from its endogenous chromosomal location, under its natural regulation. The Dynamic Proteomics interface facilitates searches for genes of interest, downloads of protein fluorescent movies and alignments of dynamics following drug addition. Each protein in the database is displayed with its annotation, cDNA sequence, fluorescent images and movies obtained by the time-lapse microscopy. The protein dynamics in the database represents a quantitative trace of the protein fluorescence levels in nucleus and cytoplasm produced by image analysis of movies over time. Furthermore, a sequence analysis provides a search and comparison of up to 50 input DNA sequences with all cDNAs in the library. The raw movies may be useful as a benchmark for developing image analysis tools for individual-cell dynamic-proteomics. The database is available at http://www.dynamicproteomics.net/.

Additional Information

© The Author(s) 2009. Published by Oxford University Press. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/ by-nc/2.5/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. Received August 15, 2009; Revised December 10, 2009; Accepted September 12, 2009. The authors thank the Kahn Family Foundation and the Israel Science Foundation for the project support. M.F.M. and E.E. are supported by the Horowitz Center for Complexity Science. The authors also thank Pierre Choukroun and Michael Green for the UNIX system administration; Malka Cymbalista and Shlomit Afgin for a technical help in the website and database construction. Funding for open access charge: The Kahn Family Foundation and the Israel Science Foundation.

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Additional details

Identifiers

PMCID
PMC2808965
Eprint ID
18306
Resolver ID
CaltechAUTHORS:20100514-095126619

Funding

Kahn Family Foundation
Israel Science Foundation
Horowitz Center for Complexity Science

Dates

Created
2010-05-24
Created from EPrint's datestamp field
Updated
2021-11-08
Created from EPrint's last_modified field