3,023 research outputs found
Precursors of Cytochrome Oxidase in Cytochrome-Oxidase-Deficient Cells of Neurospora crassa
Three different cell types of Neurospora crassa deficient in cytochrome oxidase were studied: the nuclear mutant cni-1, the cytoplasmic mutant mi-1 and copper-depleted wild-type cells.
* 1.
The enzyme-deficient cells have retained a functioning mitochondrial protein synthesis. It accounted for 12–16% of the total protein synthesis of the cell. However, the analysis of mitochondrial translation products by gel electrophoresis revealed that different amounts of individual membrane proteins were synthesized. Especially mutant cni-1 produced large amounts of a small molecular weight translation product, which is barely detectable in wild-type.
* 2.
Mitochondrial preparations of cytochrome-oxidase-deficient cells were examined for precursors of cytochrome oxidase. The presence of polypeptide components of cytochrome oxidase in the mitochondria was established with specific antibodies. On the other hand, no significant amounts of heme a could be extracted.
* 3.
Radioactively labelled components of cytochrome oxidase were isolated by immunoprecipitation and analysed by gel electrophoresis. All three cell types contained the enzyme components 4–7, which are translated on cytoplasmic ribosomes. The mitochondrially synthesized components 1–3 were present in mi-1 mutant and in copper-depleted wild-type cells. In contrast, components 2 and 3 were not detectable in the nuclear mutant cni-1. Both relative and absolute amounts of these polypeptides in the enzyme-deficient cells were quite different from those in wild-type cells.
* 4.
The components of cytochrome oxidase found in the enzyme-deficient cells were tightly associated with the mitochondrial membranes.
* 5.
Processes, which affect and may control the production of enzyme precursors or their assembly to a functional cytochrome oxidase are discussed
OCULAR CHANGES IN MONGOLISM
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/75455/1/j.1749-6632.1970.tb39372.x.pd
Sub-Sets of Cancer Stem Cells Differ Intrinsically in Their Patterns of Oxygen Metabolism
PMCID: PMC3640080This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Expression of GLUT1 and GLUT3 Glucose Transporters in Endometrial and Breast Cancers
Cancer cells have accelerated metabolism and high glucose requirements. The up-regulation of specific glucose transporters may represent a key mechanism by which malignant cells may achieve increased glucose uptake to support the high rate of glycolysis. In present study we analyzed the mRNA and protein expression of GLUT1 and GLUT3 glucose transporters by quantitative real-time polymerase chain reaction (Q-PCR) and Western blotting technique in 76 cases of endometrial carcinoma and 70 cases of breast carcinoma. SLC2A1 and SLCA2A3 mRNAs expression was found, respectively in 100% and 97.4% samples of endometrial cancers and only in 50% and 40% samples of breast cancers. In endometrial cancers GLUT1 and GLUT3 protein expression was identified in 67.1% and 30.3% of cases. Analogously, in breast cancers in 48.7% and 21% of samples, respectively. The results showed that both endometrial and breast poorly differentiated tumors (grade 2 and 3) had significantly higher GLUT1 and GLUT3 expression than well-differentiated tumors (grade 1). Statistically significant association was found between SLCA2A3 mRNA expression and estrogen and progesterone receptors status in breast cancers. GLUT1 has been reported to be involved in the uptake of glucose by endometrial and breast carcinoma cells earlier and the present study determined that GLUT3 expression is also involved. GLUT1 and GLUT3 seem to be important markers in endometrial and breast tumors differentiation
Thermodynamic Properties of the One-Dimensional Extended Quantum Compass Model in the Presence of a Transverse Field
The presence of a quantum critical point can significantly affect the
thermodynamic properties of a material at finite temperatures. This is
reflected, e.g., in the entropy landscape S(T; c) in the vicinity of a quantum
critical point, yielding particularly strong variations for varying the tuning
parameter c such as magnetic field. In this work we have studied the
thermodynamic properties of the quantum compass model in the presence of a
transverse field. The specific heat, entropy and cooling rate under an
adiabatic demagnetization process have been calculated. During an adiabatic
(de)magnetization process temperature drops in the vicinity of a field-induced
zero-temperature quantum phase transitions. However close to field-induced
quantum phase transitions we observe a large magnetocaloric effect
Dynamic Phase Transition, Universality, and Finite-size Scaling in the Two-dimensional Kinetic Ising Model in an Oscillating Field
We study the two-dimensional kinetic Ising model below its equilibrium
critical temperature, subject to a square-wave oscillating external field. We
focus on the multi-droplet regime where the metastable phase decays through
nucleation and growth of many droplets of the stable phase. At a critical
frequency, the system undergoes a genuine non-equilibrium phase transition, in
which the symmetry-broken phase corresponds to an asymmetric stationary limit
cycle for the time-dependent magnetization. We investigate the universal
aspects of this dynamic phase transition at various temperatures and field
amplitudes via large-scale Monte Carlo simulations, employing finite-size
scaling techniques adopted from equilibrium critical phenomena. The critical
exponents, the fixed-point value of the fourth-order cumulant, and the critical
order-parameter distribution all are consistent with the universality class of
the two-dimensional equilibrium Ising model. We also study the cross-over from
the multi-droplet to the strong-field regime, where the transition disappears
The relative influence of intellectual disabilities and autism on sensory impairments and physical disability:A whole‐country cohort of 5.3 million children and adults
Background:
Intellectual disabilities and autism are lifelong and often co‐occur. Little is known on their extent of independent association with sensory impairments and physical disability.
Methods:
For Scotland's population, logistic regressions investigated age–gender‐adjusted odds ratios (OR) of associations, independently, of intellectual disabilities and autism with sensory impairments and physical disability.
Results:
1,548,819 children/youth, and 3,746,584 adults. In children/youth, the effect size of intellectual disabilities and autism, respectively, was as follows: blindness (OR = 30.12; OR = 2.63), deafness (OR = 13.98; OR = 2.31), and physical disability (OR = 43.72; OR = 5.62). For adults, the effect size of intellectual disabilities and autism, respectively, was as follows: blindness (OR = 16.89; OR = 3.29), deafness (OR = 7.47; OR = 2.36), and physical disability (OR = 6.04; OR = 3.16).
Conclusions:
Intellectual disabilities have greater association with the population burden of sensory impairments/physical disability, but autism is also associated regardless of overlap with intellectual disabilities. These may impact further on communication limitations due to autism and intellectual disabilities, increasing complexity of assessments/management of other health conditions. Clinicians need to be aware of these important issues
Random walk with barriers: Diffusion restricted by permeable membranes
Restrictions to molecular motion by barriers (membranes) are ubiquitous in
biological tissues, porous media and composite materials. A major challenge is
to characterize the microstructure of a material or an organism
nondestructively using a bulk transport measurement. Here we demonstrate how
the long-range structural correlations introduced by permeable membranes give
rise to distinct features of transport. We consider Brownian motion restricted
by randomly placed and oriented permeable membranes and focus on the
disorder-averaged diffusion propagator using a scattering approach. The
renormalization group solution reveals a scaling behavior of the diffusion
coefficient for large times, with a characteristically slow inverse square root
time dependence. The predicted time dependence of the diffusion coefficient
agrees well with Monte Carlo simulations in two dimensions. Our results can be
used to identify permeable membranes as restrictions to transport in disordered
materials and in biological tissues, and to quantify their permeability and
surface area.Comment: 8 pages, 3 figures; origin of dispersion clarified, refs adde
- …