T pictured to prevent obstruction of the data points for viewing.

T pictured to prevent obstruction of the data points for viewing. doi:10.1371/journal.pone.0061300.g2X SDS Loading Buffer (100 mM Tris-HCl, 200 mM dithiothreitol, 4 w/v SDS, 0.2 bromophenol blue, 20 v/v glycerol) and was subjected to 6 SDS-PAGE. The gel was then electroblotted to a PVDF membrane, and blocked in 5 skim milk in NP-40 buffer (50 mM Tris-HCl, 150 mM NaCl, 5 mM EDTA, 0.05 v/v order Indolactam V Nonidet P-40) for 1 h at 25uC. The membrane was rinsed with NP-40 buffer and then labeled with rabbit polyclonal anti-Ply serum (1:200 dilution in NP-40 buffer) produced as described previously [44]. After a 3 h incubation at 25uC, the membrane was washed 3 times in NP-40 buffer and labeled with horseradish peroxidase (HRP) conjugated goat antirabbit IgG for 2 h at 25uC. The membrane was then washed 3 times with NP-40 buffer and developed with Pierce ECL western blotting substrate.Flow CytometryAdherent HCECs were detached from the culture flask with 0.1 trypsin-EDTA for 10 min, washed 2 times with PBS, and fixed in 3.7 paraformaldehyde (PFA) for 15 min at 25uC. The fixed cells were washed 3 times with PBS and suspended in PBS at a concentration of 106 cells/ml. Fluorescent labeling was performed as described above. The fixed cell suspension was divided into 300 ml aliquots and labeled with either AF488-labeled PlyWT, mutant Ply, heat inactivated Ply, or BSA and incubated for 30 min at 37uC. After incubation, the cells were centrifuged at 500 x g for 3 min, and the supernatant was removed. The cells were then washed 3 times with PBS before being suspended in a final 300 ml of PBS and transferred to 5 ml dilution tubes. Ply surface binding was detected using a Gallios flow cytometer with Kaluza software version 1.1 (Beckman Coulter, Miami, FL). Each experimental condition was performed in triplicate with 5,000 events per experiment.Alexa Fluor 488 LabelingBoth PlyWT and mutant Ply molecules were conjugated with Alexa Fluor 488 (AF488) tags in order to facilitate fluorescent detection. The conjugation reactions were carried out using the Alexa Fluor microscale protein labeling kit (Invitrogen Molecular Probes) according to the manufacturers instructions. The degree of labeling for each Ply type was optimized to be 3 AF488 tags per molecule of Ply. No significant difference was observed between the cytotoxicities of AF488-labeled PlyWT and unlabeled PlyWT (data not shown).Sucrose Density Gradient CentrifugationFive x 106 HCECs were collected and washed 3 times in 15755315 Trisbuffered saline (TBS; 25 mM Tris/HCl, 140 mM NaCl, pH 7.5). TBS was removed and the cells were suspended in 1 ml of incubation buffer (25 mM Tris/HCl, 140 mM NaCl, 1 mM EDTA, 1 mM PMSF, Roche Complete Protease Inhibitor cocktail, pH 8) plus 25 mg of Ply and 5 mg of biotinylated choleraPneumolysin Binds to Lipid Rafts of Corneal CellsFigure 4. Ply Surface Binding to HCECs. Flow cytometry was used to assess surface binding to HCECs. Various concentrations of AF488 labeled Ply were incubated in the presence of 3×105 fixed HCECs. AF488 labeled bovine serum albumin (BSA) and AF488 labeled heat inactivated (HI) PlyWT were included as BTZ043 chemical information controls. Data is presented as of cells with Ply surface binding compared to total cells. Each mutant was statistically compared to PlyWT and significant differences (P,0.05) are denoted as either a single asterisk (open squares) or 2 asterisks (closed circles) to account for each group. Error bars are not pictured to prevent obstruction of the data points for.T pictured to prevent obstruction of the data points for viewing. doi:10.1371/journal.pone.0061300.g2X SDS Loading Buffer (100 mM Tris-HCl, 200 mM dithiothreitol, 4 w/v SDS, 0.2 bromophenol blue, 20 v/v glycerol) and was subjected to 6 SDS-PAGE. The gel was then electroblotted to a PVDF membrane, and blocked in 5 skim milk in NP-40 buffer (50 mM Tris-HCl, 150 mM NaCl, 5 mM EDTA, 0.05 v/v Nonidet P-40) for 1 h at 25uC. The membrane was rinsed with NP-40 buffer and then labeled with rabbit polyclonal anti-Ply serum (1:200 dilution in NP-40 buffer) produced as described previously [44]. After a 3 h incubation at 25uC, the membrane was washed 3 times in NP-40 buffer and labeled with horseradish peroxidase (HRP) conjugated goat antirabbit IgG for 2 h at 25uC. The membrane was then washed 3 times with NP-40 buffer and developed with Pierce ECL western blotting substrate.Flow CytometryAdherent HCECs were detached from the culture flask with 0.1 trypsin-EDTA for 10 min, washed 2 times with PBS, and fixed in 3.7 paraformaldehyde (PFA) for 15 min at 25uC. The fixed cells were washed 3 times with PBS and suspended in PBS at a concentration of 106 cells/ml. Fluorescent labeling was performed as described above. The fixed cell suspension was divided into 300 ml aliquots and labeled with either AF488-labeled PlyWT, mutant Ply, heat inactivated Ply, or BSA and incubated for 30 min at 37uC. After incubation, the cells were centrifuged at 500 x g for 3 min, and the supernatant was removed. The cells were then washed 3 times with PBS before being suspended in a final 300 ml of PBS and transferred to 5 ml dilution tubes. Ply surface binding was detected using a Gallios flow cytometer with Kaluza software version 1.1 (Beckman Coulter, Miami, FL). Each experimental condition was performed in triplicate with 5,000 events per experiment.Alexa Fluor 488 LabelingBoth PlyWT and mutant Ply molecules were conjugated with Alexa Fluor 488 (AF488) tags in order to facilitate fluorescent detection. The conjugation reactions were carried out using the Alexa Fluor microscale protein labeling kit (Invitrogen Molecular Probes) according to the manufacturers instructions. The degree of labeling for each Ply type was optimized to be 3 AF488 tags per molecule of Ply. No significant difference was observed between the cytotoxicities of AF488-labeled PlyWT and unlabeled PlyWT (data not shown).Sucrose Density Gradient CentrifugationFive x 106 HCECs were collected and washed 3 times in 15755315 Trisbuffered saline (TBS; 25 mM Tris/HCl, 140 mM NaCl, pH 7.5). TBS was removed and the cells were suspended in 1 ml of incubation buffer (25 mM Tris/HCl, 140 mM NaCl, 1 mM EDTA, 1 mM PMSF, Roche Complete Protease Inhibitor cocktail, pH 8) plus 25 mg of Ply and 5 mg of biotinylated choleraPneumolysin Binds to Lipid Rafts of Corneal CellsFigure 4. Ply Surface Binding to HCECs. Flow cytometry was used to assess surface binding to HCECs. Various concentrations of AF488 labeled Ply were incubated in the presence of 3×105 fixed HCECs. AF488 labeled bovine serum albumin (BSA) and AF488 labeled heat inactivated (HI) PlyWT were included as controls. Data is presented as of cells with Ply surface binding compared to total cells. Each mutant was statistically compared to PlyWT and significant differences (P,0.05) are denoted as either a single asterisk (open squares) or 2 asterisks (closed circles) to account for each group. Error bars are not pictured to prevent obstruction of the data points for.