Search PubMed⌕ Search

Biomedical subjects

A van Zon

Publications and source records attributed to A van Zon.

8 recordsLinked to original sources

The vault complex.

Vaults are large ribonucleoprotein particles found in eukaryotic cells. They are composed of multiple copies of a Mr 100,000 major vault protein and two minor vault proteins of Mr 193,000 and 240,000, as well as small untranslated RNAs of 86-141 bases. The vault components are arranged into a highly characteristic hollow barrel-like structure of 35 x 65 nm in size. Vaults are predominantly localized in the cytoplasm where they may associate with cytoskeletal elements. A small fraction of vaults are found to be associated with the nucleus. As of yet, the precise cellular function of the vault complex is unknown. However, their distinct morphology and intracellular distribution suggest a role in intracellular transport processes. Here we review the current knowledge on the vault complex, its structure, components and possible functions.

Animals↗

Multiple human vault RNAs. Expression and association with the vault complex.

Human vaults are intracellular ribonucleoprotein particles believed to be involved in multidrug resistance. The complex consists of a major vault protein (MVP), two minor vault proteins (VPARP and TEP1), and several small untranslated RNA molecules. Three human vault RNA genes (HVG1-3) have been described, and a fourth was found in a homology search (HVG4). In the literature only the association of hvg1 with vaults was shown in vivo. However, in a yeast three-hybrid screen the association of hvg1, hvg2, and hvg4 with TEP1 was demonstrated. In this study we investigated the expression and vault association of different vault RNAs in a variety of cell lines, including pairs of drug-sensitive and drug-resistant cells. HVG1-3 are expressed in all cell lines examined, however, none of the cell lines expressed HVG4. This probably is a consequence of the absence of essential external polymerase III promoter elements. The bulk of the vault RNA associated with vaults was hvg1. Interestingly, an increased amount of hvg3 was bound to vaults isolated from multidrug-resistant cell lines. Our findings suggest that vaults bind the RNA molecules with different affinities in different situations. The ratio in which the vault RNAs are associated with vaults might be of functional importance.

Base Sequence↗

Health and endogenous growth.

The focus of endogenous growth theory on human capital formation and the physical embodiment of knowledge in people, suggests the integration of the growth supporting character of health production and the growth generating services of human capital accumulation in an endogenous growth framework. We show that a slow down in growth may be explained by a preference for health that is positively influenced by a growing income per head, or by an ageing population. Growth may virtually disappear for countries with high rates of decay of health, low productivity of the health-sector, or high rates of discount.

Efficiency↗

Self-motion in glass-forming polymers: a molecular dynamics study.

We present results of molecular dynamics simulations of an undercooled polymer melt, performed to study the validity of mode-coupling theory (MCT) for realistic polymer melts in general. The mean square displacements of the chain segments are computed to study the diffusion constant of the Rouse-like motion. It is shown that this diffusion constant follows a power law behavior as a function of the temperature, as predicted by the MCT. In addition, we studied the incoherent part of the intermediate scattering function and show that these functions obey the second scaling law of the MCT. We also calculated the relaxation times of the alpha-relaxation and found that they follow the same power law (gamma=2.9) as the diffusion constant. Using gamma, and the relationships given by MCT, we obtain values for a (0.27) and b (0.46) and use these exponents to describe the beta-relaxation regime. We find that the long time part of the beta-relaxation can be described accurately by the Von Schweidler relaxation over a wide range of wave numbers. In the short time regime of the beta-relaxation, no critical decay is observed.

Journal Article↗

Cerebral lesions in mice infected with Plasmodium berghei are the result of an immunopathological reaction.

Cerebral lesions in mice with Plasmodium berghei infections can be prevented by timely treatment with immune serum, by splenectomy, and by administration of dexamethasone. T cell deficient mice do not develop cerebral lesions. The results of these studies are compatible with the hypothesis that a pathological reaction is responsible for development of cerebral lesions in mice infected with P. berghei.

Animals↗