Luor 488 conjugated goat anti-human IgG fragments (for LipL32) or Alexa Fluor

Luor 488 conjugated goat anti-human IgG fragments (for LipL32) or Alexa Fluor 488 conjugated goat antirabbit IgG fragments (for FlaA2). A DAPI counterstain was used to demonstrate the presence of spirochetes. The identities of individual proteins recognized by the particular antibody reagent are indicated on the top of each column. doi:10.1371/journal.pone.0051025.gFigure 5. Membrane affinity analysis of LipL32, LipL41, LipL46 and 18325633 OmpL1. The membrane fraction of L. interrogans was treated with lysis buffer as a control or 0.1 M Na2CO3 (pH 11), 1.6 M urea, or 0.6 M NaCl for 15 min at 4uC. Samples were pelleted by centrifugation to separate the membrane pellet (P) and soluble supernatant (S), followed by gel electrophoresis (Bis-Tris 4?2 NuPage gel, Novex), and immunoblotting with specific antisera. Lane WC contained the whole cell unfractionated lysate of L. interrogans. The location of individual proteins are indicated on the right, and the positions of molecular mass standard (in kilodaltons) are indicated on the left. doi:10.1371/journal.pone.0051025.gDiscussionLipL32 is the most abundant protein in pathogenic Leptospira [17,20] and arguably the most widely studied protein in leptospirosis research [17,24,25,33?6]. The lipoprotein nature of LipL32 and its presence in outer-membrane fraction was previously reported [17]. Previous studies have also reported that LipL32 is exposed on the leptospiral surface [18]. Here we report surface-proteolysis and immunofluorescence assays performed to re-evaluate the localization of LipL32. We show that LipL32 on intact leptospires is not cleaved by Proteinase K, whereas the enzyme digests the protein efficiently in lysed cells (Fig. 1). When performed with both positive and FCCP chemical information negative controls, as we have done here, this result clearly suggests that the bulk of LipL32 is not surface exposed. To further evaluate LipL32 surface exposure, 1531364 we conducted IFA studies utilizing three different types of LipL32 antibodies. In each case, LipL32 was recognized only after the outer membranes were permeabilized with methanol (Fig. 3). To eliminate the possibility that LipL32 antibodies are recognizing only methanol-denaturated protein, the IFA was performed using different OM-permeabilization methods, showing that regardless of which method was used to perturb the OM, LipL32-specific antibodies recognize the protein only in disrupted cells (Fig. 4). While our surface localization data clearly indicate that LipL32 is not exposed on the leptospiral surface, LipL32 was confirmed as an integral membrane protein (Fig. 5). Although the membrane affinity methods do not discriminate between outer and inner membrane proteins, LipL32 has been previously localized to the outer membrane by Triton X-114 fractionation [17] and membrane vesicle fractionation [12]. LipL32 is completely solubilized by Triton X-114 fractionation, but a significant amount of LipL32 found in protoplasmic cylinder fraction byanti-FlaA2 serum was utilized to assess permeabilization efficiency, demonstrating that while methanol appears to be the most effective permeabilization agent, the three other methods also resulted in OM disruption (Fig. 4).LipL32 is associated with the leptospiral membraneMembrane affinity analysis was performed to determine whether LipL32 is associated with the lipid bilayer. Treatment of bacterial cells with lysozyme and several SPI1005 manufacturer freeze-thaw cycles, followed by centrifugation separates proteins into soluble (cytoplasmic and per.Luor 488 conjugated goat anti-human IgG fragments (for LipL32) or Alexa Fluor 488 conjugated goat antirabbit IgG fragments (for FlaA2). A DAPI counterstain was used to demonstrate the presence of spirochetes. The identities of individual proteins recognized by the particular antibody reagent are indicated on the top of each column. doi:10.1371/journal.pone.0051025.gFigure 5. Membrane affinity analysis of LipL32, LipL41, LipL46 and 18325633 OmpL1. The membrane fraction of L. interrogans was treated with lysis buffer as a control or 0.1 M Na2CO3 (pH 11), 1.6 M urea, or 0.6 M NaCl for 15 min at 4uC. Samples were pelleted by centrifugation to separate the membrane pellet (P) and soluble supernatant (S), followed by gel electrophoresis (Bis-Tris 4?2 NuPage gel, Novex), and immunoblotting with specific antisera. Lane WC contained the whole cell unfractionated lysate of L. interrogans. The location of individual proteins are indicated on the right, and the positions of molecular mass standard (in kilodaltons) are indicated on the left. doi:10.1371/journal.pone.0051025.gDiscussionLipL32 is the most abundant protein in pathogenic Leptospira [17,20] and arguably the most widely studied protein in leptospirosis research [17,24,25,33?6]. The lipoprotein nature of LipL32 and its presence in outer-membrane fraction was previously reported [17]. Previous studies have also reported that LipL32 is exposed on the leptospiral surface [18]. Here we report surface-proteolysis and immunofluorescence assays performed to re-evaluate the localization of LipL32. We show that LipL32 on intact leptospires is not cleaved by Proteinase K, whereas the enzyme digests the protein efficiently in lysed cells (Fig. 1). When performed with both positive and negative controls, as we have done here, this result clearly suggests that the bulk of LipL32 is not surface exposed. To further evaluate LipL32 surface exposure, 1531364 we conducted IFA studies utilizing three different types of LipL32 antibodies. In each case, LipL32 was recognized only after the outer membranes were permeabilized with methanol (Fig. 3). To eliminate the possibility that LipL32 antibodies are recognizing only methanol-denaturated protein, the IFA was performed using different OM-permeabilization methods, showing that regardless of which method was used to perturb the OM, LipL32-specific antibodies recognize the protein only in disrupted cells (Fig. 4). While our surface localization data clearly indicate that LipL32 is not exposed on the leptospiral surface, LipL32 was confirmed as an integral membrane protein (Fig. 5). Although the membrane affinity methods do not discriminate between outer and inner membrane proteins, LipL32 has been previously localized to the outer membrane by Triton X-114 fractionation [17] and membrane vesicle fractionation [12]. LipL32 is completely solubilized by Triton X-114 fractionation, but a significant amount of LipL32 found in protoplasmic cylinder fraction byanti-FlaA2 serum was utilized to assess permeabilization efficiency, demonstrating that while methanol appears to be the most effective permeabilization agent, the three other methods also resulted in OM disruption (Fig. 4).LipL32 is associated with the leptospiral membraneMembrane affinity analysis was performed to determine whether LipL32 is associated with the lipid bilayer. Treatment of bacterial cells with lysozyme and several freeze-thaw cycles, followed by centrifugation separates proteins into soluble (cytoplasmic and per.