Ow the R620W polymorphism modifies the function of this complex and contributes to the induction ofRegulation of TCR Signaling by LYP/CSK Complexautoimmunity, in this work we have analyzed LYP/CSK interaction and its relevance for TCR signaling.Materials and Methods Antibodies and ReagentsTissue culture 117793 reagents were from Lonza (Verviers, Belgium). The 25033180 anti-hemagglutinin (HA) mAb was from Covance (Berkely, CA, USA). The anti-LCK mouse Ab (3A5), anti-GST Ab, antimyc Ab (9E10), anti-Erk2 Ab (C154), anti-Fyn Ab (6A406) and anti-CSK rabbit polyclonal Ab (C-20) were from Santa Cruz Biotechnology Inc. (Santa Cruz, CA, USA). The anti-CD3 (UCHT1), anti-CD28 (clone CD28.2), anti-Abl and anti-CSK mouse Ab were from BD Pharmingen (Franklin Lakes, NJ, USA). The anti-phosphotyrosine 4G10 mAb was from Millipore (Billerica, MA, USA).The anti-LYP goat polyclonal Ab was from R D Systems, Inc. (Minneapolis, MN, USA). The anti-phospho-p38 Ab was from Cell Signaling Technology Inc., (Beverly, MA, USA).The anti-phospho-Erk Ab was from Promega (Fitchburg, WI, USA).Pull-down of GST fusion Finafloxacin proteins was done with Glutathion sepharose beads (GE Healthcare, Buckinghamshire, UK.) incubated with the clarified lysates for 2 h. The complexes were then washed and processed as explained above for the IP. Blots were scanned with the GS-800 Densitometer (Bio-Rad Laboratories, CA, USA) and analyzed with the image analysis software Quantity One (Bio-Rad Laboratories, CA, USA). Data are reported as arbitrary units.Luciferase AssaysTransfection of Jurkat T cells and assays for LUC activity were performed as 
described previously [19,20]. Briefly, 206106 Jurkat cells were transfected with 20 mg empty pEF vector or the indicated plasmids, along with 3 mg of NFAT/AP-1-luc (or other reporters) and 0.5 mg of a Renilla luciferase reporter for normalization. Cells were stimulated with anti-CD3 plus anti-CD28 Abs 24 h after transfection for the last 6 h. Cells were lysed then and processed to measure the LUC activity with the Dual Luciferase system (Promega, CA USA) according to the manufacturer’s instructions.Plasmids and MutagenesisStandard molecular biology techniques were used to generate the different constructions used in this study. Site-directed mutagenesis was done with the QuickChange Mutagenesis Kit (Agilent-Stratagene, CA, USA) following the manufacturer instructions. All constructions and mutations were verified by nucleotide sequencing.Flow Cytometry and ImmunohistochemistryJurkat cells were stimulatd with soluble anti-CD3 plus antiCD28 Abs for 24 hours and were stained with Phycoerythrin (PE)labeled anti-CD25 or PE-IgG2b isotype control (Immunostep, Salamanca, Spain). Data were acquired on a Gallios Flow Cytometer instrument (Beckman Coulter, Inc. CA, USA) and analysis was carried out with WinMDI software.Cell Culture and TransfectionsHEK293 were maintained at 37uC in Dulbecco’s modified Eagle’s medium supplemented with 10 FBS, 2 mM L-glutamine, 100 16574785 U/ml penicillin G, and 100 mg/ml streptomycin. Transient transfection of HEK293 cells was carried out using the calcium phosphate precipitation method [18]. JCam1.6, P116 and Jurkat T leukemia 
cells were kept at logarithmic growth in RPMI 1640 medium supplemented with 10 FBS, 2 mM Lglutamine, 1 mM sodium pyruvate, non essential aa, 100 U/ml penicillin G, and 100 mg/ml streptomycin. Transfection of Jurkat T cells was performed by electroporation as described previously [19]. PBLs were isolated from buffy coats of healthy d.Ow the R620W polymorphism modifies the function of this complex and contributes to the induction ofRegulation of TCR Signaling by LYP/CSK Complexautoimmunity, in this work we have analyzed LYP/CSK interaction and its relevance for TCR signaling.Materials and Methods Antibodies and ReagentsTissue culture reagents were from Lonza (Verviers, Belgium). The 25033180 anti-hemagglutinin (HA) mAb was from Covance (Berkely, CA, USA). The anti-LCK mouse Ab (3A5), anti-GST Ab, antimyc Ab (9E10), anti-Erk2 Ab (C154), anti-Fyn Ab (6A406) and anti-CSK rabbit polyclonal Ab (C-20) were from Santa Cruz Biotechnology Inc. (Santa Cruz, CA, USA). The anti-CD3 (UCHT1), anti-CD28 (clone CD28.2), anti-Abl and anti-CSK mouse Ab were from BD Pharmingen (Franklin Lakes, NJ, USA). The anti-phosphotyrosine 4G10 mAb was from Millipore (Billerica, MA, USA).The anti-LYP goat polyclonal Ab was from R D Systems, Inc. (Minneapolis, MN, USA). The anti-phospho-p38 Ab was from Cell Signaling Technology Inc., (Beverly, MA, USA).The anti-phospho-Erk Ab was from Promega (Fitchburg, WI, USA).Pull-down of GST fusion proteins was done with Glutathion sepharose beads (GE Healthcare, Buckinghamshire, UK.) incubated with the clarified lysates for 2 h. The complexes were then washed and processed as explained above for the IP. Blots were scanned with the GS-800 Densitometer (Bio-Rad Laboratories, CA, USA) and analyzed with the image analysis software Quantity One (Bio-Rad Laboratories, CA, USA). Data are reported as arbitrary units.Luciferase AssaysTransfection of Jurkat T cells and assays for LUC activity were performed as described previously [19,20]. Briefly, 206106 Jurkat cells were transfected with 20 mg empty pEF vector or the indicated plasmids, along with 3 mg of NFAT/AP-1-luc (or other reporters) and 0.5 mg of a Renilla luciferase reporter for normalization. Cells were stimulated with anti-CD3 plus anti-CD28 Abs 24 h after transfection for the last 6 h. Cells were lysed then and processed to measure the LUC activity with the Dual Luciferase system (Promega, CA USA) according to the manufacturer’s instructions.Plasmids and MutagenesisStandard molecular biology techniques were used to generate the different constructions used in this study. Site-directed mutagenesis was done with the QuickChange Mutagenesis Kit (Agilent-Stratagene, CA, USA) following the manufacturer instructions. All constructions and mutations were verified by nucleotide sequencing.Flow Cytometry and ImmunohistochemistryJurkat cells were stimulatd with soluble anti-CD3 plus antiCD28 Abs for 24 hours and were stained with Phycoerythrin (PE)labeled anti-CD25 or PE-IgG2b isotype control (Immunostep, Salamanca, Spain). Data were acquired on a Gallios Flow Cytometer instrument (Beckman Coulter, Inc. CA, USA) and analysis was carried out with WinMDI software.Cell Culture and TransfectionsHEK293 were maintained at 37uC in Dulbecco’s modified Eagle’s medium supplemented with 10 FBS, 2 mM L-glutamine, 100 16574785 U/ml penicillin G, and 100 mg/ml streptomycin. Transient transfection of HEK293 cells was carried out using the calcium phosphate precipitation method [18]. JCam1.6, P116 and Jurkat T leukemia cells were kept at logarithmic growth in RPMI 1640 medium supplemented with 10 FBS, 2 mM Lglutamine, 1 mM sodium pyruvate, non essential aa, 100 U/ml penicillin G, and 100 mg/ml streptomycin. Transfection of Jurkat T cells was performed by electroporation as described previously [19]. PBLs were isolated from buffy coats of healthy d.