Abstract
To explore the relative roles of protein-binding partners vs. lipid modifications in controlling membrane targeting of a typical peripheral membrane protein, Galpha(z), we directed its binding partner, betagamma, to mislocalize on mitochondria. Mislocalized betagamma directed wild-type Galpha(z) and a palmitate-lacking Galpha(z) mutant to mitochondria but did not alter localization of a Galpha(z) mutant lacking both myristate and palmitate. Thus, in this paradigm, a protein-protein interaction controls targeting of a peripheral membrane protein to the proper compartment, whereas lipid modifications stabilize interactions of proteins with membranes and with other proteins.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Amino Acid Substitution
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Animals
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Biological Transport
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CHO Cells
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Cricetinae
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Cricetulus
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GTP-Binding Protein alpha Subunits*
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GTP-Binding Protein beta Subunits*
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GTP-Binding Protein gamma Subunits*
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GTP-Binding Proteins / metabolism*
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Heterotrimeric GTP-Binding Proteins / genetics
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Heterotrimeric GTP-Binding Proteins / metabolism*
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Intracellular Membranes / metabolism*
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MAP Kinase Signaling System
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Membrane Lipids / metabolism
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Membrane Proteins / metabolism*
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Microscopy, Fluorescence
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Mitochondria / metabolism
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Mutagenesis, Site-Directed
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Myristic Acid / metabolism
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Palmitates / metabolism
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Recombinant Fusion Proteins / metabolism
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Transfection
Substances
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G-protein Beta gamma
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GTP-Binding Protein alpha Subunits
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GTP-Binding Protein beta Subunits
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GTP-Binding Protein gamma Subunits
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Membrane Lipids
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Membrane Proteins
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Palmitates
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Recombinant Fusion Proteins
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Myristic Acid
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GTP-Binding Proteins
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Heterotrimeric GTP-Binding Proteins