Fig. 2.
Fig. 2. Surface expression of αvβ3mutants in transiently transfected 293 cells. / (A) The surface expression of transfected αvβ3 was analyzed 2 days after transfection by flow cytometry. Cells expressing WT or mutant αvβ3 were incubated with 5 μg/mL αvβ3 complex-specific mAb LM609 for 30 minutes on ice and then washed once. Bound antibodies were detected by FITC-conjugated goat F(ab′)2 antimouse IgG. Relative amounts of the binding were normalized to a 100% value for LM609 binding to cells expressing WT αvβ3. The results are representative of 3 separate experiments. (B) Immunoprecipitation showing the surface expression of transfected αvβ3. Transiently transfected cells were surface-labeled with sulfo-NHS-biotin and lysed in the lysing buffer containing 1% Triton X-100. WT or mutant αvβ3 was precipitated with LM609 (specific for the αvβ3 complex) and separated on a 6% sodium dodecyl sulfate polyacrylamide gel under reducing conditions. After transfer, a membrane was incubated with peroxidase-conjugated avidin and developed with chemiluminescence. The results are representative of 3 separate experiments.

Surface expression of αvβ3mutants in transiently transfected 293 cells.

(A) The surface expression of transfected αvβ3 was analyzed 2 days after transfection by flow cytometry. Cells expressing WT or mutant αvβ3 were incubated with 5 μg/mL αvβ3 complex-specific mAb LM609 for 30 minutes on ice and then washed once. Bound antibodies were detected by FITC-conjugated goat F(ab′)2 antimouse IgG. Relative amounts of the binding were normalized to a 100% value for LM609 binding to cells expressing WT αvβ3. The results are representative of 3 separate experiments. (B) Immunoprecipitation showing the surface expression of transfected αvβ3. Transiently transfected cells were surface-labeled with sulfo-NHS-biotin and lysed in the lysing buffer containing 1% Triton X-100. WT or mutant αvβ3 was precipitated with LM609 (specific for the αvβ3 complex) and separated on a 6% sodium dodecyl sulfate polyacrylamide gel under reducing conditions. After transfer, a membrane was incubated with peroxidase-conjugated avidin and developed with chemiluminescence. The results are representative of 3 separate experiments.

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