These data identify the JNK1 pathway as an important target in understanding lung immunity

ressed from the T7 promoter in pET19b. Restriction sites are underlined. Both sequences were PCR amplified using Platinum Taq DNA polymerase as directed. PCR products were subcloned into pGEM-T, digested using either NdeI and XhoI or NcoI and XhoI, and ligated into similarly digested pET19b. Final vectors were sequence verified using T7 promoter and T7 terminator primers at the Uniformed Services University Biomedical Instrumentation Center and transformed into E. coli C43 to create E. coli ATM1172 and E. coli ATM1173. C43 carrying pET19b also was constructed for control experiments. diluted 1:1000 was substituted for the anti-Hsp60 antibody. Blots were developed using Supersignal West Pico Chemiluminescent Substrate and visualized using an ImageQuant LAS 4000. 3 H-biotin transport assays Western blot detection of proteins Detection of biotinylated proteins. To detect biotinylated proteins from mid-developmental cycle Chlamydia, confluent L2 cell monolayers grown in 60 mm tissue culture dishes were infected with EBs at an MOI of 1 as previously described. At 20 hours post infection, the medium was removed and cells were washed with PBS. Cells were then lysed by the addition of 200 ml of Laemmli buffer containing 25 units benzonase and 16 Halt LGX818 Protease Inhibitor Cocktail. After incubating for five minutes on ice, samples were collected and b-mercaptoethanol was added prior to boiling. For the detection of biotinylated proteins in EBs, EBs were lysed in Laemmli buffer containing 16 Halt Protease Inhibitor Cocktail and b-mercaptoethanol. E. coli control samples were obtained from cultures grown in Luria Bertani broth, which were harvested by centrifugation and lysed with Laemmli buffer containing 16 Halt Protease Inhibitor Cocktail and b-mercaptoethanol. Samples were run on 12% SDSPAGE gels ) and then transferred to nitrocellulose. Blots were blocked with 1% BSA/PBS, washed with 0.05% Tween 20/ PBS and then incubated with Ultrasensitive Streptavidin-Peroxidase Polymer diluted 1:1000 in 1% BSA/0.05% Tween 20/PBS. After probing for biotinylated proteins, blots were washed with 0.05% Tween 20/PBS, incubated with Supersignal West Pico Chemiluminescent Substrate and visualized using an ImageQuant LAS 4000. Detection of Hsp60 and His-tagged BioY. Samples prepared for biotinylated protein analysis also were used for Hsp60 Western blot analysis. After transferring proteins to nitrocellulose, blots were blocked with 5% milk/TBS and probed with a mouse anti-Hsp60 antibody diluted 1:1000 in 5% milk/ 0.05%Tween-20/TBS. Blots were then washed with 0.05%Tween-20/TBS, probed with a HRP-conjugated goat anti-mouse antibody, and finally washed again in 0.05%Tween-20/TBS. To detect His-tagged BioY, E. coli ATM1172 was grown in 2xTY medium with 100 mg/ ml ampicillin to an OD600 nm of,0.6 and then induced with 1 mM IPTG at 37uC for 2.5 hours. Bacteria were then pelleted and lysed in Laemmli buffer containing 16 Halt Protease Inhibitor Cocktail and b-mercaptoethanol, boiled, and run on 12% SDS-PAGE gels. Protein was transferred to nitrocellulose and blotted as described for Hsp60 with the exception that a mouse anti-His tag antibody To measure biotin transport, E. coli ATM1172, E. coli ATM1173, or E. coli ATM1135 were grown overnight in 2xTY medium with 100 mg/ml ampicillin at 37uC. Bacteria were then subcultured into 2xTY containing 100 mg/ml ampicillin and 0.1 mM IPTG and grown at 37uC to an OD600 nm of,1. Cultures were placed on ice and then pelleted to conc