Abstract
Containing four LIM domains and an N-terminal half LIM domain, FHL2 has been predicted to have an adaptor function in the formation of higher order molecular complexes in the nucleus and the cytoplasm of cells. We expressed recombinant FHL2 in insect cells using the baculovirus system and used it to isolate direct or indirect interaction partners from the cytosolic fraction of fibroblasts by affinity chromatography. These were identified by their peptide mass fingerprints using MALDI-TOF mass spectrometry. Cytoskeleton-associated proteins present among the bound proteins were shown to co-localise with FHL2 in cell lamellipodia by indirect immunofluorescence staining.
Copyright 2004 Wiley-Liss, Inc.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Animals
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Cell Line
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Chromatography, Affinity
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Circular Dichroism
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Cytoplasm / chemistry
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Cytoplasm / metabolism
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Homeodomain Proteins / chemistry*
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Homeodomain Proteins / genetics
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Homeodomain Proteins / isolation & purification*
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Homeodomain Proteins / metabolism
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Humans
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Insecta
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LIM-Homeodomain Proteins
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Molecular Sequence Data
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Muscle Proteins / chemistry*
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Muscle Proteins / genetics
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Muscle Proteins / isolation & purification*
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Muscle Proteins / metabolism
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Protein Binding
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Protein Structure, Tertiary
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Proteins / analysis
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Proteins / chemistry
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Proteins / isolation & purification
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Pseudopodia / metabolism
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Recombinant Fusion Proteins / chemistry
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Recombinant Fusion Proteins / genetics
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Recombinant Fusion Proteins / isolation & purification
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Recombinant Fusion Proteins / metabolism
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Transcription Factors / chemistry*
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Transcription Factors / genetics
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Transcription Factors / isolation & purification*
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Transcription Factors / metabolism
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Transfection
Substances
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FHL2 protein, human
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Homeodomain Proteins
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LIM-Homeodomain Proteins
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Muscle Proteins
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Proteins
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Recombinant Fusion Proteins
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Transcription Factors