(A) Sensitised acceptor emission FRET analysis of positive and negative control cell lines. The positive BGJ398 control consisted of cells expressing CFP coupled to YFP. The negative control consisted of cells expressing individual CFP and YFP proteins encoded by different plasmids. While the positive control cells demonstrated high FRET efficiency (47.4%±1.6), the negative control showed 0% FRET efficiency. (B) Equal amount of WT YFP-ζ and MUT YFP-ζ proteins were expressed in COS-7 cells upon transfection as detected by anti-YFP Western blot analysis. (C) Acceptor photobleaching FRET analysis was performed using images collected in three independent experiments,
as described in the supplementary methods section. *P<0.0001. Figure S5. Mutations in the ζ RRR motifs do not affect its conformation but impair its association with actin. (A) Mutations in the RRR motifs restore TCR cell surface expression. ζ-deficient T-cell clones stably expressing the WT (17 and 14) or MUT (8 and 15) ζ were tested for cell surface NVP-BEZ235 TCR expression using anti-CD3e antibodies and FACS analysis. WT and MUT ζ expressing T-cell clones were lysed and immunoprecipitated with four different antibodies directed against various epitopes (“a”-“d”) localized within the ζ intracytoplasmic domain (B). Samples were separated on reduced SDS-PAGE
and immunoblotted for ζ (C). (D) T-cells expressing the MUT ζ failed to undergone percipitataion with actin. WT and MUT transfected T-cell clones or splenocytes from WT and transgenic (ζD66–150), mice were lysed, immunoprecipitated with anti-actin antibodies. Samples were immunoblotted with
pheromone antibodies directed against the indicated proteins. Ab = antibody with no lysate. Figure S6. WT and MUT T-cell clones exhibit a similar immediate TCR-mediated activation pattern. (A) WT and MUT T-cell clones exhibit a similar pattern of ζ isoforms induced upon short activation. Cells were activated with anti-CDe and anti-CD28 antibodies, lysed, and the non-cska fraction was subjected to immunoblotting with anti-ζ antibodies. (B) A similar ZAP-70 phosphorylation pattern was observed in both WT and MUT T-cell clones upon brief activation. The cells were activated as described in (A), lysed, immunoprecipitated with anti-ZAP-70 antibodies, separated on reduced SDS-PAGE and immunoblotted with anti-ZAP-70 or anti-phosphotyrosine antibodies. (C) A similar LAT phosphorylation pattern was observed in both WT and MUT T-cell clones upon brief activation. The cells were activated as described in (A), lysed, separated on reduced SDS-PAGE and immunoblotted with anti-LAT or anti-pLAT antibodies. Figure S7. Cska and non-cska expression during T-cell activation. (A) Total cska and non-cska ζ expression during T-cell activation. Mouse splenocytes were activated with anti-CD antibodies for various intervals, lysed, the cska and non-cska fractions were separated and subjected to immunoblotting with anti-ζ antibodies.
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