Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: EC:3.4.25.1 (proteasome)
 28,817 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Modifier of cell adhesion protein (MOCA; previously called presenilin [PS] binding protein) is a DOCK180-related molecule, which interacts with PS1 and PS2, is localized to brain areas involved in Alzheimer's disease (AD) pathology, and is lost from the soluble fraction of sporadic Alzheimer's disease (AD) brains. Because PS1 has been associated with gamma-secretase activity, MOCA may be involved in the regulation of beta-amyloid precursor protein (APP) processing. Here we show that the expression of MOCA decreases both APP and amyloid beta-peptide secretion and lowers the rate of cell-substratum adhesion. In contrast, MOCA does not lower the secretion of amyloid precursor-like protein (APLP) or several additional type 1 membrane proteins. The phenotypic changes caused by MOCA are due to an acceleration in the rate of intracellular APP degradation. The effect of MOCA expression on the secretion of APP and cellular adhesion is reversed by proteasome inhibitors, suggesting that MOCA directs nascent APP to proteasomes for destruction. It is concluded that MOCA plays a major role in APP metabolism and that the effect of MOCA on APP secretion and cell adhesion is a downstream consequence of MOCA-directed APP catabolism. This is a new mechanism by which the expression of APP is regulated.
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PMID:A novel mechanism for the regulation of amyloid precursor protein metabolism. 1209 89

A microdosimetric one hit detector model has been applied to calculate dose response, energy response and relative efficiency of thermoluminescent LiF:Mg,Cu,P (MCP-N), CaF2:Tm (TLD-300) and ESR alanine detectors on radiation of different qualities. For each detector type two model parameters, the target size and the saturation parameter, alpha, have been derived. Using those parameters and the microdosimetric distributions in nanometre size targets calculated using Monte Carlo track structure codes TRION and MOCA-14 it was possible to predict a great variety of experimental data for photons, X rays, beta electrons, protons, alpha particles and heavy ions. Due to a good reproducibility of experimental data some solid state detectors might be useful to test biophysical models of radiation action. Furthermore, these models can give some insight into the physics of radiation action in solid state detectors such as the range of charge interaction, energy levels etc.
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PMID:Microdosimetric one hit detector model for calculation of dose and energy response of some solid state detectors. 1219 33

Lithium fluoride thermoluminescence (TL) detectors, with different Li composition (Li-6 and Li-7) and various activators (LiF:Mg,Ti, LiF:Mg,Cu,P), are widely used for dosimetry in space. The primary radiation field in space is composed of fast electrons, protons and heavy charged particles (HCP). By its interaction with the structures of the spacecraft, this field may be modified inside the crew cabin. Therefore, calibration of TL detectors against a dose of gamma-rays is not sufficient for relating the TL readout to absorbed dose or to quantities relevant in radiation protection, without suitable correction. We introduce and calculate the detection efficiency, eta, relative to gamma-ray dose, of lithium fluoride detectors after proton and heavy charged particle (HCP) irradiation. We calculate eta for MCP-N (LiF:Mg,Cu,P) and for MTS-N (LiF:Mg,Ti) using microdosimetric models. The microdosimetric distributions used in these models (for HCP of charges between Z=1 to Z=8 and in the energy range between 0.3 MeV/amu and 20 MeV/amu) are calculated using an analytical model, based on the results of Monte Carlo simulated charged particle tracks using the MOCA-14 code. The ratio etaMCP-N/etaMTS-N for protons of stopping power (in water) below 10 keV/microm lies in the range between 0.65 and 1.0 and for HCP with Z>1--between 0.3 and 0.6. The stopping power of the particle is found not to be a unique parameter to scale the response of TL detectors. The combination of response of LiF:Mg,Cu,P and LiF:Mg,Cu,P detectors can be more suitable for a dose correction in space radiation fields.
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PMID:Modeling the response of thermoluminescence detectors exposed to low- and high-LET radiation fields. 1279 31