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Mechanism and Cellular Applications of a Green Fluorescent Protein-based Halide Sensor

Jayaraman, Sujatha, Haggie, Peter, Wachter, Rebekka M., Remington, S.James, Verkman, A.S.·2000·Journal of Biological Chemistry

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FIG. 1 Sensitivity of YFP-H148Q spectral properties to Cl 2 . A , dependence of YFP-H148Q fluorescence on pH at indicated [Cl 2 ]. B , dependence of relative YFP-H148Q fluorescence on [Cl 2 ] or [I 2 ] at pH 7.5. C , influence of Cl 2 on YFP-H148Q absorption spectrum at pH 6.4. D , influence of fluoride on YFP-H148Q CD spectrum.
FIG. 1 Sensitivity of YFP-H148Q spectral properties to Cl 2 . A , dependence of YFP-H148Q fluorescence on pH at indicated [Cl 2 ]. B , dependence of relative YFP-H148Q fluorescence on [Cl 2 ] or [I 2 ] at pH 7.5. C , influence of Cl 2 on YFP-H148Q absorption spectrum at pH 6.4. D , influence of fluoride on YFP-H148Q CD spectrum.CC-BY · From the PDF
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FIG. 3 YFP-H148Q expression in transfected Swiss 3T3 fibroblasts. A , fluorescence confocal micrograph showing expression in cytoplasm and nucleus. B , dependence of intracellular YFP-H148Q fluorescence on pH. Fluorescence pH titration (at 0 Cl 2 ) in Swiss 3T3 fibroblasts expressing YFP-H148Q and CFTR. Cells were perfused with high K 1 buffer containing ionophores at indicated pH (see 'Materials and Methods'). C , fluorescence Cl 2 titration (at pH 7.4) using high K 1 buffer containing ionophores and indicated [Cl 2 ] (see 'Materials and Methods').
FIG. 3 YFP-H148Q expression in transfected Swiss 3T3 fibroblasts. A , fluorescence confocal micrograph showing expression in cytoplasm and nucleus. B , dependence of intracellular YFP-H148Q fluorescence on pH. Fluorescence pH titration (at 0 Cl 2 ) in Swiss 3T3 fibroblasts expressing YFP-H148Q and CFTR. Cells were perfused with high K 1 buffer containing ionophores at indicated pH (see 'Materials and Methods'). C , fluorescence Cl 2 titration (at pH 7.4) using high K 1 buffer containing ionophores and indicated [Cl 2 ] (see 'Materials and Methods').CC-BY · From the PDF
FIG. 4 CFTR-mediated Cl 2 transport detected by changes in intracellular YFP-H148Q fluorescence. A , CFTR-expressing cells were perfused with PBS containing forskolin to activate CFTR. Where indicated Cl 2 was replaced with gluconate ( top ), NO3 2 ( middle ), or I 2 ( bottom ). B , forskolin-stimulated Cl 2 /I 2 transport. Cells ( top , CFTRexpressing; bottom , control) were initially perfused with a phosphate buffer containing 100 mM I 2 followed by perfusion with PBS and then addition of 20 m M forskolin as indicated.
FIG. 4 CFTR-mediated Cl 2 transport detected by changes in intracellular YFP-H148Q fluorescence. A , CFTR-expressing cells were perfused with PBS containing forskolin to activate CFTR. Where indicated Cl 2 was replaced with gluconate ( top ), NO3 2 ( middle ), or I 2 ( bottom ). B , forskolin-stimulated Cl 2 /I 2 transport. Cells ( top , CFTRexpressing; bottom , control) were initially perfused with a phosphate buffer containing 100 mM I 2 followed by perfusion with PBS and then addition of 20 m M forskolin as indicated.CC-BY · From the PDF

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Metadata

Authors
Jayaraman, S., Haggie, P., Wachter, R. M., Remington, S. J., & Verkman, A. S.
Venue
Journal of Biological Chemistry
Publisher
Elsevier BV
Published
2000-03
Volume
275
Issue
9
Pages
6047-6050
ISSN
0021-9258
Cited by
264
References
0
Language
en

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CoChat. (2026). Citation check: Mechanism and Cellular Applications of a Green Fluorescent Protein-based Halide Sensor. https://app.cochat.ai/papers/10.1074/jbc.275.9.6047
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Jayaraman, S., Haggie, P., Wachter, R. M., Remington, S. J., & Verkman, A. S. (2000). Mechanism and Cellular Applications of a Green Fluorescent Protein-based Halide Sensor. Journal of Biological Chemistry. https://doi.org/10.1074/jbc.275.9.6047