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.

Slides:



Advertisements
Similar presentations
Calculating Percentages using a Calculator © T Madas.
Advertisements

CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS BiC BioCentrum-DTU Technical University of Denmark Cleavage sites and binding affinities.
Transglutaminase-mediated oligomerization of the fibrin(ogen) αC domains promotes integrin-dependent cell adhesion and signaling by Alexey M. Belkin, Galina.
SPR characterization of the specific interaction between AuNP–Pep1 and HEWL. (A) Binding of AuNPs functionalized with 20 Pep1 and different numbers of.
Inhibition of PDGFR-β downstream signaling events by flavones.
Generation of a dual-labeled fluorescence biosensor for Crk-II phosphorylation using solid-phase expressed protein ligation  Graham J Cotton, Tom W Muir 
ORF2S antigenically overlaps with virions and interferes with antibody-mediated neutralization but not entry of HEV. (A) Location of six distinct antigenic.
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.
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.
The interaction of FAM49B and Rac.
p110-free p85 is present in MEFs and certain murine tissues.
DHEA(S) and Allo protected rat chromaffin cells in culture against serum deprivation-induced apoptosis. DHEA(S) and Allo protected rat chromaffin cells.
Despite a relatively small amount of PI3Kβ being associated with activated PDGFRs, it generates a more substantial proportion of the PIP3 that accumulates.
P85α and p110δ, but not other subunits, interact preferentially in vivo. p85α and p110δ, but not other subunits, interact preferentially in vivo. (A) Compares.
PGAM5 associates with and activates ASK1.
Themis acts to increase phosphorylation of Shp1.
Phosphatase activity associated with Themis and Shp1 in response to different affinity peptide ligands. Phosphatase activity associated with Themis and.
Themis interacts with Shp2 when Shp1 is genetically deleted.
Absolute quantitation of class IA PI3K subunits and heterodimers in MEFs. (A) Immunoblot of endogenous p85α in lysates of MEFs (clones 1 or 2, genotypes.
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.
Human osteoarthritic chondrocytes are impaired in matrix metalloproteinase-13 inhibition by IFN-γ due to reduced IFN-γ receptor levels  R. Ahmad, M. El.
ATP-Dependent Effector-like Functions of RIG-I-like Receptors
S534 phosphorylation affects DNA binding and gene expression by NF-κB at late time points through regulation of p65 stability. S534 phosphorylation affects.
IRS1-Independent Defects Define Major Nodes of Insulin Resistance
PDGFRα GBM primary cultures demonstrate titratable and temporal DOX-inducible expression of hPDGF-A and receptor activation. PDGFRα GBM primary cultures.
Feng Zhang, Jiazhong Shi, Chunjing Bian, Xiaochun Yu  Cell Reports 
Effect of mutations on GS-E affinity, ATPase activity.
Distinct Roles for CTD Ser-2 and Ser-5 Phosphorylation in the Recruitment and Allosteric Activation of Mammalian mRNA Capping Enzyme  C.Kiong Ho, Stewart.
Volume 41, Issue 2, Pages (January 2011)
Volume 17, Issue 6, Pages (December 1996)
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.
Calcium induced CHGB aggregation and single particle analysis of CHGB dimers. Calcium induced CHGB aggregation and single particle analysis of CHGB dimers.
Neurotensin receptor–1 and –3 complex modulates the cellular signaling of neurotensin in the HT29 cell line  Stéphane Martin, Valérie Navarro, Jean Pierre.
Effect of agonists on receptor mobility.
Longitudinal analysis of ZIKV E–specific memory B cell responses in the DENV-experienced donors. Longitudinal analysis of ZIKV E–specific memory B cell.
Volume 8, Issue 5, Pages (November 2001)
The Relationship of MHC-Peptide Binding and T Cell Activation Probed Using Chemically Defined MHC Class II Oligomers  Jennifer R Cochran, Thomas O Cameron,
The B2′B3 region confers the binding phenotype of full-length TcdB.
Volume 9, Issue 4, Pages (April 2011)
Volume 8, Issue 5, Pages (November 2001)
UBA1 is recruited to DNA and promotes Chk1 phosphorylation.
Volume 11, Issue 4, Pages (April 2003)
Rescue of the sel-12 Egl phenotype by PS1 and PS1ΔE9 expressed from arrays formed at a concentration of 2 μg/ml. Rescue of the sel-12 Egl phenotype by.
(Upper) Blind-to-controls generalization performance: prediction accuracies observed when the classifier was trained on the auditory trials from the blind.
dsRBDs 3 and 4 of hStau1 dimerize on the RNA.
TRADD is recruited to the TLR4 signaling complex upon LPS stimulation.
TRAF4 is required for EGFR activation in response to EGF stimulation.
CKL family is involved in the circadian clock.
ZFAND5 associates with 26S proteasomes and slows their migration in native PAGE. (A) Purified 26S proteasomes bind directly to ZFAND5. 26S proteasomes.
Activation of PKR by the PBM decoy peptide.
Distribution of phosphosites and PDGFRα activity in primary cultures.
Structure and receptor-binding properties of SCH-C.
Accumulation of asialoglycoproteins, agalactoglycoproteins, and Man-terminated N-glycans during blood protein aging. Accumulation of asialoglycoproteins,
ZFAND5 stimulates proteasomes and promotes overall protein degradation in MEF, HeLa, and HEK293 cells. ZFAND5 stimulates proteasomes and promotes overall.
The interaction of Toll ECD with hcSpätzle supports an asymmetric binding mode of Spätzle C106. The interaction of Toll ECD with hcSpätzle supports an.
Fig. 5. Expression of either dFMRP or human FMRP does not induce eIF2α phosphorylation.(A) Analysis of eIF2α phosphorylation upon dFMRP expression. Expression.
hStau1 dimerizes on the RNA.
FAK tyrosine phosphorylation is unaffected by loss of LAR activity.
Figure 4 DNM1 mutations affect protein levels and self-dimerization (A) HeLa cells were transfected with green fluorescent protein (GFP)-tagged mutant.
Loss of LAR phosphatase activity is associated with decreased adhesion complex formation. Loss of LAR phosphatase activity is associated with decreased.
FACT has moderate nucleosome assembly activity.
How upland and lowland alleles contribute to the optimal genotype at each field site. How upland and lowland alleles contribute to the optimal genotype.
Fig. 3 BIC1 and BIC2 inhibit early photoreactions of cryptochromes.
Synergistic WNT1 and WNT7B signaling is downstream of LRP6 phosphorylation and β-catenin stabilization. Synergistic WNT1 and WNT7B signaling is downstream.
Efficient and preferential pairing of cysteine-modified TCRs
PKCζ is tyrosine phosphorylated by EGF and contributes to EGF-induced activation of ERK in Mef cells. PKCζ is tyrosine phosphorylated by EGF and contributes.
Volume 47, Issue 1, Pages e4 (October 2018)
The Relationship of MHC-Peptide Binding and T Cell Activation Probed Using Chemically Defined MHC Class II Oligomers  Jennifer R Cochran, Thomas O Cameron,
Presentation transcript:

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 PDGFRs with higher affinity than the p85-p110 dimers at low levels of receptor activation. (A) The amounts of p110-free p85 associated with PDGFRs following stimulation with PDGF-BB (1 min). Levels are expressed as a percentage of the total p85 associated with PDGFRs (as presented in Fig. 5). (B) Absolute amounts of p110-free p85 recovered with PDGFRs, quantified by mass spec (“measured”) compared with the amount predicted if no difference in affinity, between p110-free and heterodimeric-p85, existed (“expected”). Expected values were calculated by multiplying the amount of total p85 recruited to PDGFR (Fig. 5C) with the percentage p110-unbound p85 in that clone (Fig. 3D). (C) Amounts of p110-free p85β in streptavidin pull-downs from MEFs expressing p85βavi/avi, with (+) or without (−) prior pull-down of PDGFRs. The amount is expressed as a percentage of the total amount of p85β pulled down or as absolute levels. (D) Estimating the apparent affinity of interaction between recombinant, purified, monomeric p85α or p85α-p110α dimers and PYPs using fluorescence polarization. A given protein preparation was equilibrated with a fluorescein-labeled PYP (Fluor-GpYMDMS, 2 nM) and a doubly phosphorylated, nonfluorescent PYP was titrated into the mixture to the indicated concentrations. The data are all means, ±SD, from three independent experiments. Statistically significant at *P < 0.05 and **P < 0.01. N. Tsolakos et al. PNAS 2018;115:48:12176-12181 ©2018 by National Academy of Sciences