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. 2013 Apr 1;110(16):6406–6411. doi: 10.1073/pnas.1219909110

Fig. 2.

Fig. 2.

SGMS1GT cells are defective in influenza viral particles production. (A) Equal numbers of KBM7 and SGMS1GT cells were infected with influenza virus (A/WSN/33) at an MOI of 0.1. At 24 h after infection, cells were pulse-labeled with [35S]-methionine/cysteine for 30 min and total cell lysates were analyzed by SDS/PAGE and autoradiography. (B) Cells were infected as described in A, and viral titers from the supernatant were measured by a fluorescent focus assay on MDCK cells. (C) Cells were incubated at different MOIs with Alexa 647-labeled influenza virus for 30 min on ice, followed by cytofluorimetry. (D) Flow cytometry of Alexa 647-positive cells upon exposure of KBM7, SGMS1GT, and SLC25A2GT with CTx-Alexa647 for 15 min on ice. SLC25A2GT cells are defective in GM1 biosynthesis and hence CTx is unable to bind to these cells. (E) Confocal images of KBM7 and SGMS1GT cells incubated with Alexa 647-labeled influenza virus and Alexa 488-CTx for 30 min on ice. FFU, focus-forming unit.