Moco-dependent localization of SO

Slides:



Advertisements
Similar presentations
ERCC6L2 Mutations Link a Distinct Bone-Marrow-Failure Syndrome to DNA Repair and Mitochondrial Function  Hemanth Tummala, Michael Kirwan, Amanda J. Walne,
Advertisements

Fig. 3. A dynamic STUB1-TF interaction depends on the uremic status.
Volume 22, Issue 5, Pages (May 2012)
TAT-mediated Delivery of LAD Restores Pyruvate Dehydrogenase Complex Activity in the Mitochondria of Patients with LAD Deficiency  Matan Rapoport, Ann.
Volume 16, Issue 5, Pages (December 2004)
Insulin regulates the expression and intra-membrane proteolysis of the recombinant HA-pSREBP-1c-Flag protein in McA-RH7777 cells Insulin regulates the.
Enhancing 1α-Hydroxylase Activity with the 25-Hydroxyvitamin D-1α-Hydroxylase Gene in Cultured Human Keratinocytes and Mouse Skin  Tai C. Chen, Xue Hong.
Volume 14, Issue 1, Pages (January 2004)
Coiled Coils Direct Assembly of a Cold-Activated TRP Channel
Volume 20, Issue 5, Pages (August 2017)
A JNK-Dependent Pathway Is Required for TNFα-Induced Apoptosis
Fig. 2 Fas controls IL-1RA–sEV secretion in murine MSCs.
Volume 20, Issue 14, Pages (July 2010)
Volume 18, Issue 10, Pages (March 2017)
Volume 17, Issue 5, Pages (November 2002)
ZBTB48 is required for MTFP1 expression
The CHCH domain is necessary for mitochondrial import of CHCHD10
Volume 62, Issue 4, Pages (May 2016)
Evaluation of LC3 and ATG13 dynamics in AS-stimulated microglial cells using live-imaging. Evaluation of LC3 and ATG13 dynamics in AS-stimulated microglial.
The histidine-rich loop regulates accessibility of the active site and RDEL motif in vivo. The histidine-rich loop regulates accessibility of the active.
A highly conserved six-amino-acid region in the C-terminal CT domain of MARCH8 is responsible for its ability to downregulate TfR. A highly conserved six-amino-acid.
The C-terminal membrane-proximal region of MARCH8 interacts with TfR.
Fig. 5. Expression of either dFMRP or human FMRP does not induce eIF2α phosphorylation.(A) Analysis of eIF2α phosphorylation upon dFMRP expression. Expression.
Fig. 3. Characterization of unclassified cells (UCs).
ICAM-1 forms distinct complexes with filamin B, α-actinin-4 and cortactin. ICAM-1 forms distinct complexes with filamin B, α-actinin-4 and cortactin. (A)
GFP–Sec61b mRNA competes with t-ftz mRNA for the ribosome-binding sites on the ER. (A,B) COS7 cells were transfected with plasmid containing a test gene.
Figure 4 DNM1 mutations affect protein levels and self-dimerization (A) HeLa cells were transfected with green fluorescent protein (GFP)-tagged mutant.
ArfGAP1 expression alters GBF1 recruitment to Golgi membranes.
Reconstitution of GBF1 recruitment to Golgi membranes in a cell-free assay. Reconstitution of GBF1 recruitment to Golgi membranes in a cell-free assay.
Crim1 colocalizes with integrin and activates the integrin-FAK-ERK signaling pathway. Crim1 colocalizes with integrin and activates the integrin-FAK-ERK.
Transbilayer distribution of cholesterol in the plasma membrane is defective in staurosporine-treated cells. Transbilayer distribution of cholesterol in.
High-affinity mutants of β3 integrin fail to stimulate RhoA activity and fibronectin fibrillogenesis. High-affinity mutants of β3 integrin fail to stimulate.
Interaction of periostin with ECM molecules.
Ezrin in its open, activated conformation binds and colocalizes with MISP at the cell cortex. Ezrin in its open, activated conformation binds and colocalizes.
N-cadherin deficient cells do not adhere or migrate.
14-3-3γ phosphorylated at S59 by Lats2 in response to UV damage.
The K86M mutation in ABCG2 results in a non-functional transporter.
The SIM domain of RAD51 is required for HR
Expression of active Rho partially rescues Erk1/2 activation and peripheral FA phenotype in RIAM-knockdown cells. Expression of active Rho partially rescues.
Lysine residues in the cytoplasmic region of TfR are involved in the MARCH8-induced downregulation of TfR. Lysine residues in the cytoplasmic region of.
Impact of LAMP interaction on TAPL function.
Effect of the siRNA-mediated knockdown of endogenous MARCH8 on the expression levels of MARCH8 substrates, TfR and CD98, in HepG2 cells. Effect of the.
BRG1 interacts with RAD52 and regulates its accumulation at DSB sites during homologous recombination repair. BRG1 interacts with RAD52 and regulates its.
Proliferation on soft matrices is decoupled from myosin light chain phosphorylation, cell tractions, and focal adhesions. Proliferation on soft matrices.
Misfolding mutations impair the BRCA1 nuclear aggregation in yeast and the BRCA1 nuclear localization in human cells. Misfolding mutations impair the BRCA1.
Fig. 1. Rnd2 and Rnd3 induce stress fibres whereas Rnd1 reduces stress fibres in endothelial cells.(A) Rnd mRNAs are expressed in HUVECs. Total RNA was.
Fig. 6. RhoB is required for Rnd3-induced stress fibre formation
Segments R1, R3, R6 and R7, and GTPase activity of Mfn2ΔTM are necessary for mitochondrial fragmentation in COS7 cells. Segments R1, R3, R6 and R7, and.
EPLIN also plays a crucial role in the apical extrusion of RasV12-transformed cells. EPLIN also plays a crucial role in the apical extrusion of RasV12-transformed.
WT MARCH8, but not the CS mutant, specifically ubiquitinates and downregulates TfR. WT MARCH8, but not the CS mutant, specifically ubiquitinates and downregulates.
Fig. 4. Tetracycline-regulated expression of ClC-5 in the HEK293 cells stably expressing gastric H+,K+-ATPase.(A) Alignments of rat ClC-5, human ClC-5,
Fig. 7. Analysis of dFMRP kinetics in dFMRP granules by FRAP
Volume 34, Issue 5, Pages (June 2009)
Expression of IP3R subtypes in HEK cells.
Effect of M-cadherin RNAi on apoptosis in confluent C2C12 myoblasts.
Vps36 interacts with Smo in the absence of Hh
Role of Src and PTP-PEST in upregulation of tyrosine phosphorylation of paxillin and FAK. (A) Mock and D11 cells were pre-incubated with PP2 or PP3 (10 µM,
Generation of an inducible form of FOXN1.
GOLPH3 interacts with COG complex proteins.
Exosomal transfer of sortilin to a target cell.
4E-BP is present in an 80 kDa complex in unfertilized eggs.
Volume 27, Issue 7, Pages e5 (May 2019)
Mutant MFN2 proteins have normal half-lives and are properly localized to mitochondria. Mutant MFN2 proteins have normal half-lives and are properly localized.
Volume 23, Issue 2, Pages (August 2005)
Fig. 3 C9ORF72 interacts with SMCR8 in a DENN domain–dependent manner.
Cdk1 Negatively Regulates Midzone Localization of the Mitotic Kinesin Mklp2 and the Chromosomal Passenger Complex  Stefan Hümmer, Thomas U. Mayer  Current.
Volume 19, Issue 8, Pages (April 2009)
KDM4A levels affect the distribution of translation initiation factors
BRAF in-frame deletions mainly function as BRAF homodimers.
Mitochondrial import of CerS1 from smooth ER mediates lethal mitophagy
Presentation transcript:

Moco-dependent localization of SO Moco-dependent localization of SO. (A,B) Expression of WT-SO in HEK-293 cells (A) and Moco-deficient fibroblasts (B) 48 h after transfection. Moco-dependent localization of SO. (A,B) Expression of WT-SO in HEK-293 cells (A) and Moco-deficient fibroblasts (B) 48 h after transfection. Cells were stained for SO with an anti-SO antibody (green) and examined by confocal laser scanning microscopy. Mitochondria were stained with MitoTracker Red CMXRos. Representative images of three independent experiments are shown. Scale bars: 10 µm. Cartoons illustrate the status of cofactor saturation and oligomerization: L, leader sequence; H, heme; Mo, Moco; DD, dimerization domain. (C) Quantification of Moco saturation in 100 pmol of purified WT-SO and SO-R367H-K380R variant using HPLC FormA analysis. Error bars represent standard deviations of three independent experiments. (D,E) Size exclusion chromatography of purified WT-SO (D) and SO-R367H-K380R (E) variant eluting mainly as a dimer and monomer, respectively. Red lines illustrate heme absorption at 413 nm. Representative profiles of four independent experiments are shown. (F) Expression of SO-R367H-K380R variant in HEK-293 cells. Transfection and staining was conducted as described for A and B. Scale bar: 10 µm. (G) Pearson correlation coefficients were determined by means of Perkin Elmer's VOLOCITY software. Five images were separately analysed; average and standard deviations are shown. (H) WT and SO-R367H-K380R were expressed in HEK-293 cells for 48 hours. Cytosolic (C) and mitochondrial (M) fractions were separated from each other and total amounts of protein were determined in both fractions. Representative amounts of mitochondrial and cytosolic protein were loaded on a 12% SDS gel for western blotting. Gels were stained for VDAC as a mitochondrial and for gephyrin (GEPH) as a cytosolic marker. Myc-tagged, recombinantly expressed SO was stained using anti-myc antibody. Similar results were obtained in three independent experiments. Julian M. Klein, and Guenter Schwarz J Cell Sci 2012;125:4876-4885 © 2012. Published by The Company of Biologists Ltd