Document Detail


The hard cell: from proteomics to a whole cell model.
MedLine Citation:
PMID:  17555749     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Proteomics has provided a wealth of data related to the nature of the proteome, including subcellular location, copy number, interaction partners and protein complexes. This raises the question of whether it is feasible to combine these data, together with other data related to overall cellular structure, to construct a static picture of the cell. In this minireview, we discuss these data, and the issues of turning them into whole cell models.
Authors:
Matthew J Betts; Robert B Russell
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Review     Date:  2007-05-30
Journal Detail:
Title:  FEBS letters     Volume:  581     ISSN:  0014-5793     ISO Abbreviation:  FEBS Lett.     Publication Date:  2007 Jun 
Date Detail:
Created Date:  2007-06-11     Completed Date:  2007-08-30     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0155157     Medline TA:  FEBS Lett     Country:  Netherlands    
Other Details:
Languages:  eng     Pagination:  2870-6     Citation Subset:  IM    
Affiliation:
Structural and Computational Biology Unit, European Molecular Biology Laboratory, Meyerhofstrasse 1, 69117 Heidelberg, Germany.
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MeSH Terms
Descriptor/Qualifier:
Cells / metabolism*
Genomics
Humans
Models, Biological*
Multiprotein Complexes
Proteomics*
Two-Hybrid System Techniques
Chemical
Reg. No./Substance:
0/Multiprotein Complexes

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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