Viewing. doi:10.1371/journal.pone.0061300.gtoxin b (CTxb), which binds to the common lipid raft constituent ganglioside GM1 of eukaryotic cell membranes. The cell suspension was incubated on ice for 4 h after which 40 ml of 25 TX100 was added and mixed 22948146 thoroughly (final concentration 1 TX100). The mixture was incubated an additional 1 h on ice. The solution was passed through a small gauge needle 20 times and then centrifuged at 10,000 x g for 5 min at 4uC. The supernatant was transferred to a new microcentrifuge tube, and 70 sucrose was added to a final concentration of 40 sucrose. The sample was layered under a 10?0 discontinuous sucrose gradient in a 5 ml ultracentrifuge tube at a ratio of 1.5:2.5:1. The gradient was centrifuged at 4uC for 18 h at 300,000 x g. Fractions were collected from the top in 400 ml increments. Fractions were spotted on a nitrocellulose membrane, blocked with 5 skim milk in NP-40 buffer for 1 h, and labeled with either HRP-conjugated streptavidin to detect CTxb, or anti-Ply rabbit polyclonal serum followed by HRP-conjugated goat anti-rabbit IgG to detect Ply. The blot was visualized using Pierce ECL western blotting substrate.ResultsPrevious studies that focused on Pfo, a related CDC that shares 42 amino acid homology with Ply, have pinpointed several important amino acids that are involved in interacting with the lipid environment of the host membrane during initial Teriparatide web binding [26,45]. These residues include A401, A437, W464, and L491, and correspond to A370, A406, W433, and L460 in Ply [26,46]. In Pfo, each of these amino acid residues are located at the tip of one of 4 loops structures found in domain 4 which extend out from the protein to interact with the host membrane. A sequence alignment of domain 4 from Ply and Pfo reveals that the loop residues from Pfo are conserved in Ply, and many of the surrounding residues around both A370 and L460 are also conserved (Figure 1E). Structural diagrams show the positions of the domain 4 loops relative to one another (Figure 1A-D). The R-groups from the highlighted amino acids of L1-L3 extend away from the interior of the molecule and presumably enter the lipophilic environment of the host cell membrane. Based on the observed homology and relative positions of each amino acid, we engineered 2 amino acid substitution mutants at the apex of each loop structure. We chose to substitute both glutamate and glycine in order to 1.) prevent the loop from entering the lipid environment of the host membrane (glutamate), and 
2.) observe the effect of removing the R-group from each mutation site (glycine). We also included PlyW433F since this mutation is classically studied and a wide array of information is readily available on its lytic PD1-PDL1 inhibitor 1 behavior in various models. Each PlyStatistical AnalysesExperimental results were analyzed using the statistical analysis system (SAS) for computers (SAS Institute, Cary, NC) version 9.2. All experimental groups were compared using a nonparametric one-way analysis of variance, and any P-value , 0.05 was considered significant.Pneumolysin Binds to Lipid Rafts of Corneal CellsFigure 5. Ply Oligomerization Behavior. Ply molecules were incubated either in the presence or absence of HCECs in a total volume of 20 ml before being directly mixed with SDS loading buffer and electrophoresed through a 6 SDS polyacrylamide gel with or without boiling. The gel was ??blotted to a PVDF membrane, blocked in 5 skim milk, and sequentially labeled with 1.Viewing. doi:10.1371/journal.pone.0061300.gtoxin b (CTxb), which binds to the common lipid raft constituent ganglioside GM1 of eukaryotic cell membranes. The cell suspension was incubated on ice for 4 h after which 40 ml of 25 TX100 was added and mixed 22948146 thoroughly (final concentration 1 TX100). The mixture was incubated an additional 1 h on ice. The solution was passed through a small gauge needle 20 times and then centrifuged at 10,000 x g for 5 min at 4uC. The supernatant was transferred to a new microcentrifuge tube, and 70 sucrose was added to a final concentration of 40 sucrose. The sample was layered under a 10?0 discontinuous sucrose gradient in a 5 ml ultracentrifuge tube at a ratio of 1.5:2.5:1. The gradient was centrifuged at 4uC for 18 h at 300,000 x g. Fractions were collected from the top in 400 ml increments. Fractions were spotted on a nitrocellulose membrane, blocked with 5 skim milk in NP-40 buffer for 1 h, and labeled with either HRP-conjugated streptavidin to detect CTxb, or anti-Ply rabbit polyclonal serum followed by HRP-conjugated goat anti-rabbit IgG to detect Ply. The blot was visualized using Pierce ECL western blotting substrate.ResultsPrevious studies that focused on Pfo, a related CDC that shares 42 amino acid homology with Ply, have pinpointed several important amino acids that are involved in interacting with the lipid environment of the host membrane during initial binding [26,45]. These residues include A401, A437, W464, and L491, and correspond to A370, A406, W433, and L460 in Ply [26,46]. In Pfo, each of these amino acid residues are located at the tip of one of 4 loops structures found in domain 4 which extend out from the protein to interact with the host membrane. A sequence alignment of domain 4 from Ply and Pfo reveals that the loop residues from Pfo are conserved in Ply, and many of the surrounding residues around both A370 and L460 are also conserved (Figure 1E). Structural diagrams show the positions of the domain 4 loops relative to one another (Figure 1A-D). The R-groups from the highlighted amino acids of L1-L3 extend away from the interior of the molecule and presumably enter the lipophilic environment of the host cell membrane. Based on the observed homology and relative positions of each amino acid, we engineered 2 amino acid substitution mutants at the apex of each loop structure. We chose to substitute both glutamate and glycine in order to 1.) prevent the loop from entering the lipid environment of the host membrane (glutamate), and 2.) observe the effect of removing the R-group from each mutation site (glycine). We also included PlyW433F since this mutation is classically studied and a wide array of information is readily available on its lytic behavior in various models. Each PlyStatistical AnalysesExperimental results were analyzed using the statistical analysis system (SAS) for computers (SAS 
Institute, Cary, NC) version 9.2. All experimental groups were compared using a nonparametric one-way analysis of variance, and any P-value , 0.05 was considered significant.Pneumolysin Binds to Lipid Rafts of Corneal CellsFigure 5. Ply Oligomerization Behavior. Ply molecules were incubated either in the presence or absence of HCECs in a total volume of 20 ml before being directly mixed with SDS loading buffer and electrophoresed through a 6 SDS polyacrylamide gel with or without boiling. The gel was ??blotted to a PVDF membrane, blocked in 5 skim milk, and sequentially labeled with 1.
