Literature DB >> 14662390

Protein fragment complementation strategies for biochemical network mapping.

Stephen W Michnick1.   

Abstract

The organization of biochemical networks that make up the living cell can be defined by studying the dynamics of protein-protein interactions. To this end, experimental strategies based on protein fragment complementation assays (PCAs) have been used to map biochemical networks and to identify novel components of these networks. Pharmacological perturbations of the interactions can be observed, and the resulting pharmacological profiles and subcellular locations of interactions allow each gene product to be 'placed' at its relevant point in a network. Network mapping by PCA could be used with, or instead of, traditional target-based drug discovery strategies to increase the quantity and quality of information about the actions of small molecules on living cells and the intricate networks that make up their chemical machinery.

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Year:  2003        PMID: 14662390     DOI: 10.1016/j.copbio.2003.10.014

Source DB:  PubMed          Journal:  Curr Opin Biotechnol        ISSN: 0958-1669            Impact factor:   9.740


  17 in total

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7.  Common and specific properties of herpesvirus UL34/UL31 protein family members revealed by protein complementation assay.

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Journal:  Nucleic Acids Res       Date:  2014-04-11       Impact factor: 16.971

9.  Functional interactions between Mldp (LSDP5) and Abhd5 in the control of intracellular lipid accumulation.

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10.  Small-molecule-based nanoassemblies as inducible nanoprobes for monitoring dynamic molecular interactions inside live cells.

Authors:  Sangkyu Lee; Kyoung Hu Lee; Jae-Seok Ha; Seung-Goo Lee; Tae K Kim
Journal:  Angew Chem Int Ed Engl       Date:  2011-07-27       Impact factor: 15.336

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