Key result
Tagging NCX1 with CFP or YFP preserves exchanger properties and sensitivity to cytoplasmic ions.
Insertion of CFP or YFP into the large intracellular loop of the NCX1 protein does not impair exchanger properties, providing a useful tool for studying its biological properties in intact cells.
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Supports fluorescent NCX1 constructs for intact-cell studies; leaves open translation to in vivo or clinical models.
The cardiac sarcolemmal Na+-Ca2+ exchanger (NCX1) influences cardiac contractility by extruding Ca2+ from myocytes. As a Ca2+ efflux mechanism, the exchanger plays a prominent role in Ca2+ homeostasis. To track NCX1 and study changes in conformation, NCX1 was tagged with derivatives of green fluorescent protein. Cyan (CFP) and yellow (YFP) fluorescent proteins were used for both visualization of the protein in HEK cells and fluorescent resonance energy transfer (FRET). CFP or YFP was inserted at position 266, 371, 467, or 548 of the large intracellular loop of NCX1 located between transmembrane segments 5 and 6. These constructs were tested for functional activity and visualized for cell surface expression. All constructs were targeted to the plasma membrane. Transport properties were assessed by both 45Ca2+ uptake and electrophysiological measurements. The fluorescent-tagged exchangers had similar biophysical properties to the wild type NCX1. Unexpectedly, all constructs retain their sensitivity to regulation by cytoplasmic Na+ and Ca2+ ions. FRET analysis indicates the proximity of NCX1 to plasma membrane phosphatidylinositol 4,5-bisphosphate. These results indicate that insertion of CFP or YFP into the large intracellular loop of NCX1 protein does not impair exchanger properties. These constructs will be useful to further characterize the biological properties of the exchanger in intact cells.
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Ottolia et al. (2006) studied this question. Fluorescent-tagged NCX1 (CFP or YFP) vs. Wild type NCX1 was evaluated on Functional activity, cell surface expression, and transport properties. Insertion of CFP or YFP into the large intracellular loop of the NCX1 protein did not impair exchanger properties, retaining sensitivity to regulation by cytoplasmic Na+ and Ca2+ ions.
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