Phosphatase activity associated with Themis and Shp1 in response to different affinity peptide ligands. Phosphatase activity associated with Themis and.

Slides:



Advertisements
Similar presentations
Volume 6, Issue 4, Pages (April 1997)
Advertisements

A novel SHP-1/Grb2–dependent mechanism of negative regulation of cytokine-receptor signaling: contribution of SHP-1 C-terminal tyrosines in cytokine signaling.
Posttranslational regulation of ETV5 and c-JUN in neurons.
(A) Heat map showing expression changes during in vitro differentiation of nscs to astrocytes. (A) Heat map showing expression changes during in vitro.
Schematic representation of possible effects of different factors on systemic resilience. Schematic representation of possible effects of different factors.
IP-MS identifies FAM49B interacting protein Rac.
DHEA(S) and Allo induced the phosphorylation of PKC in serum-deprived PC12 cells. DHEA(S) and Allo induced the phosphorylation of PKC in serum-deprived.
HDAC3, but not HDAC2 is in complex with tau protein.
Pretreatment of VSV-GPΔ to form VSV-GP19K rescues infection in the α5β1-integrin-negative CHO cells. Pretreatment of VSV-GPΔ to form VSV-GP19K rescues.
RGFP-966 decreases HDAC3 activity and is not cytotoxic.
Structure-based ligand design toward a selective M3R antagonist.
Principal component analysis of the GO category composition of all genes in each genome/transcriptome and WGD paralogs. Principal component analysis of.
DHEA(S) and Allo induced the expression of the antiapoptotic Bcl-2 proteins in serum-deprived PC12 cells. DHEA(S) and Allo induced the expression of the.
WCI evolve as organisms become more complex.
Lyn Physically Associates With the Erythropoietin Receptor and May Play a Role in Activation of the Stat5 Pathway by Hiroshi Chin, Ayako Arai, Hiroshi.
PGAM5 is a protein Ser/Thr phosphatase that activates ASK1.
P110-free p85 is recruited to PDGFRs with higher affinity than the p85-p110 dimers at low levels of receptor activation. p110-free p85 is recruited to.
DHEA(S) and Allo protected rat chromaffin cells in culture against serum deprivation-induced apoptosis. DHEA(S) and Allo protected rat chromaffin cells.
GPR124 promotes cell migration.
Despite a relatively small amount of PI3Kβ being associated with activated PDGFRs, it generates a more substantial proportion of the PIP3 that accumulates.
Phosphatase activity of PGAM5 is required for activation of ASK1.
Antisense oligonucleotides against the Bcl-2 transcript reversed the cytoprotective effects of DHEA(S) and Allo on serum-deprived PC12 cells. Antisense.
PGAM5 associates with and activates ASK1.
Themis acts to increase phosphorylation of Shp1.
Klotho reduction causes macrophage invasion into the CP
Thymic phenotype of Themis−/− Shp1 cKO mice is similar to that of Themis−/− mice. Thymic phenotype of Themis−/− Shp1 cKO mice is similar to that of Themis−/−
Themis interacts with Shp2 when Shp1 is genetically deleted.
Phosphatase activity associated with Themis is due to its association with Shp1. Phosphatase activity associated with Themis is due to its association.
Phosphatase activity associated with Shp1 is reduced in Themis−/− thymocytes. Phosphatase activity associated with Shp1 is reduced in Themis−/− thymocytes.
Volume 22, Issue 2, Pages (February 2005)
RGFP-966 increases H4K12 acetylation in HEK/APPsw cells.
Comparison of cytokine profiles induced by ChiLob 7/4 and TLR ligands in ex vivo whole-blood stimulation assays. Comparison of cytokine profiles induced.
The K594ScFv-SEA-D227A fusion protein targets CTL to lyse EA
Effects of neuropeptide treatment on APC stimulation of Ag-specific T cells. Effects of neuropeptide treatment on APC stimulation of Ag-specific T cells.
Volume 36, Issue 6, Pages (June 2012)
Expression of NCoR1∆ID in PAX8−/− mice does not reverse repression of T3-positive target genes. qPCR on the indicated pituitary (A) and neuronal (B) genes.
Effect of the temperature-sensitive mutation hsp90G17OD on the activity of the c-src regulatory kinase Csk and on the maturation of c-srcK295M at the semirestrictive.
In vivo BrdUrd incorporation kinetics of KTSL−/lo and KTSL− cells.
Sleep/wake phenotype of S551D mutant mice.
Effect of agonists on receptor mobility.
ICSBP stimulates GAS reporter activity in JAK/STAT-pathway-deficient cells. 2fTGH, U3A, U4A, and γ1A cells were cotransfected with the WT GAS reporter.
TIMP-2 Mediated Inhibition of Angiogenesis
T cell–intrinsic STING inhibits cell cycle progression of T cells.
HDAC11 regulates CCL2 expression by recruiting PU.1.
Activation of Gα subunit chimeras with noncognate C termini.
Excision of N7-methylguanine by AlkZ.
Peptide release is not impacted by phosphorothioate modification at interface of the P-site and A-site codons. Peptide release is not impacted by phosphorothioate.
TRADD is recruited to the TLR4 signaling complex upon LPS stimulation.
Acquisition of eyelid CRs during peripheral (vibrissae) followed by central (S1 areas for vibrissae or hind limb) CS, or vice versa. Acquisition of eyelid.
C-terminal JM-B of EGFR is required for EGF-induced recruitment of TRAF4 to EGFR. (A) The HSQC spectra of 100 μM 15N-labeled TRAF4-TRAF in the absence.
Activation of PKR by the PBM decoy peptide.
AMRs in the turnover of secreted proteins.
Structure and receptor-binding properties of SCH-C.
ZFAND5 stimulates proteasomes and promotes overall protein degradation in MEF, HeLa, and HEK293 cells. ZFAND5 stimulates proteasomes and promotes overall.
TNAP and IAP t1/2s and N-glycan remodeling following zanamivir treatment. TNAP and IAP t1/2s and N-glycan remodeling following zanamivir treatment. (A.
Stimulation of H2O2 production in L. stagnalis haemocytes by laminarin
BAP1 deficiency results in thymic atrophy and loss of thymocyte populations. BAP1 deficiency results in thymic atrophy and loss of thymocyte populations.
Model of Shp2-Ras-Sprouty2 signaling in lens and lacrimal gland development. Model of Shp2-Ras-Sprouty2 signaling in lens and lacrimal gland development.
Fluorescence assays of diameter dependent cellular toxicity.
Induction of IL-3–secreting CD4+ T cells.
Result of coincubation assays with peptide-loaded target cells, Jurkat effector cells, and bs-868Z11-CD3 at six different concentrations. Result of coincubation.
Vaginal CD11c+ DCs from IL-17A−/− mice are impaired in potentiating Th17 responses because of diminished IL-1β production. Vaginal CD11c+ DCs from IL-17A−/−
Cytotoxicity of p5399–107-induced CTL cells.
The differential susceptibility to CTL-induced lysis does not involve Melan-A antigen expression. The differential susceptibility to CTL-induced lysis.
TET2 interacts with KLF1 transcription factor.
PAP- and PA2024-specific CTLs at week 0 (prior to sipuleucel-T infusion) and at weeks 6 and 26 post–sipuleucel-T treatment. PAP- and PA2024-specific CTLs.
ABT-100 inhibits PI3K activity and p85 tyrosine phosphorylation.
Induction of OVA-specific CTLs by DCs
VEGF165 stimulates migration of HMVECs
Varying the MHC-I affinity, TCR affinity or antigen dose alters the phenotype of CD8 T cells ex vivo. Varying the MHC-I affinity, TCR affinity or antigen.
Presentation transcript:

Phosphatase activity associated with Themis and Shp1 in response to different affinity peptide ligands. Phosphatase activity associated with Themis and Shp1 in response to different affinity peptide ligands. Tyrosine phosphatase activity assay with (A) immunoprecipitated Themis from OT-I CTLs in response to different affinity peptide ligands using Themis−/− thymocytes as a negative control. (B) Immunoprecipitated Shp1 from OT-I CTLs in response to the use of different affinity peptide ligands along with unstimulated CTLs. (C) Immunoprecipitated Shp1 from CTLs made from OT-I Themis+/+ and OT-I Themis−/−, comparing unstimulated and OVA-stimulated cells. (D) Immunoprecipitated Shp1, showing reduction in Shp1 activity in OT-I β2m−/−Themis−/− thymocytes compared with OT-I β2m−/−Themis+/+ thymocytes in response to different stimulations along with unstimulated control. (E) Immunoprecipitated Themis in OT-I β2m−/−Themis+/+ thymocytes in response to stimulations using different affinity peptide ligands and OT-I β2m−/−Themis−/− thymocytes as a negative control. All of the stimulations were done for 90 s. Data are representative of three independent experiments. Unpaired t test with mean ± SD. *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001. Monika Mehta et al. PNAS 2018;115:48:E11331-E11340 ©2018 by National Academy of Sciences