688 research outputs found
Identification of RNA molecules by specific enzyme digestion and mass spectrometry: software for and implementation of RNA mass mapping
The idea of identifying or characterizing an RNA molecule based on a mass spectrum of specifically generated RNA fragments has been used in various forms for well over a decade. We have developed software—named RRM for ‘RNA mass mapping’—which can search whole prokaryotic genomes or RNA FASTA sequence databases to identify the origin of a given RNA based on a mass spectrum of RNA fragments. As input, the program uses the masses of specific RNase cleavage of the RNA under investigation. RNase T1 digestion is used here as a demonstration of the usability of the method for RNA identification. The concept for identification is that the masses of the digestion products constitute a specific fingerprint, which characterize the given RNA. The search algorithm is based on the same principles as those used in peptide mass fingerprinting, but has here been extended to work for both RNA sequence databases and for genome searches. A simple and powerful probability model for ranking RNA matches is proposed. We demonstrate viability of the entire setup by identifying the DNA template of a series of RNAs of biological and of in vitro transcriptional origin in complete microbial genomes and by identifying authentic 16S ribosomal RNAs in a ‘small ribosomal subunit RNA’ database. Thus, we present a new tool for a rapid identification of unknown RNAs using only a few picomoles of starting material
Studies on the mode of action of hydrallazine and reserpine
Hydrallazine and reserpine are used in the treatment of hypertension and reserpine is also employed in the treatment of certain forms of mental illness. Hypotheses regarding the mode of action of these drugs are numerous. Thus hydrallazine is believed to act on the vasometer centre and reserpine to depress central sympathetic tone. Reserpine is also believed to mediate its actions by liberating noradrenaline and 5-hydroxytryptamine from the brain and, in the case of noradrenaline, from the arteries. The work described in this thesis, undertaken to clarify some aspects of the mode: of action of these drugs at cellular level. Experimental evidence has indicated that hydrallazine, dihydrallazine and related compounds did not antagonise certain pressor reflexes - notably the pressor responses due to central vagal stimulation, bilateral carotid occlusion and anoxia. This speaks against their having a central site and mechanism of action, because if this were so, all pressure refluxes mediated via the central nervous system should, he antagonised or depressed. This does not, however rule out the possibility that hydrallazine acts specifically upon certain cell groups in the central nervous system. Hydrallazine antagonised the pressor effect of adrenaline more than those of noradrenaline, and the antagonism of this drug to some pressor reflexes only was explained by assuming that there are quantitative variations in the proportions of the two humoral agents secreted during the initiation of these reflexes. The fact that hypertension caused by constant infusion of a solution of adrenaline was promptly brought back to normal levels by hydrallazine, also favours a peripheral site of action for this drug. Many of the effects of hydrallazine and reserpine can be explained by assuming that both drugs interfere with the normal energy-yielding mechanisms of the smooth muscle cell. It has been shown that hydrallazine has an effect upon carbohydrate metabolism which underlies its actions upon isolated arterial smooth muscle. Intermediate a of carbohydrate metabolism antagonised hydrallazine depression of drug-induced contractions of arterial smooth muscle. The reserpine effect was so persistent that the tissue did not recover. Anoxia and cyanide also antagonised drug-induced contractions of arterial smooth muscle. Intermediates of carbohydrate metabolism gave protection against anoxia and not against cyanide. The use of hydrallazine was, in effect analogous to rendering the tissue anoxic. Reserpine did not have marked effects on tissue respiration while hydrallazine depressed it. Reserpine was found to cause in vivo inhibition of oxidative phosphorylation in rat brain and livery since the ATP/ADP ratio was significantly lowered. Hydrallazine had similar effects in rat brain and liver. Neither drug influenced the, adenosine nucleotide levels in rat skeletal muscle and heart. On the basis of this experimental evidence it has been suggested that hydrallazine may interfere with biological oxidation and reserpine with oxidative phosphorylation. It has been shown that reserpine depleted the adrenal medulla of catechol amines and ATP in roughly the same proportions. Since the characteristic breakdown products of ATP (ADP and AMP) were not found as they were: found in brain and liver it is suggested that ATP possesses a specialised function in the storage or release of catechol amines from this gland. 4. Inhibitors of metabolism, such as cyanide and have marked effects on the transport of sodium and potassium ions in tissues. Roserpine was found to have practically no effect either upon the release of potassium or on the uptake of potassium and sodium. Hydrallazine, however, increased the release of potassium. It decreased potassium retention but increased sodium retention. Cyanide and aside increased potassium release but anoxia and IMP had no effect. On the other hand, cyanide, aside, Die and anoxia had marked effects on sodium and potassium uptakes Which usually , varied inversely. Thus a reduction in the efficiency of the enzymes controlling metabolism may reduce the ability of muscle to retain potassium, resulting in the release of this ion. Hydrallazine formed chelates with different metals, and the iron-hydrallazine chelate was shown to be inert. Hydrallazine in high doses inhibited catalase, depressed the iron-catalysed oxidation of cysteine to cystine and was shown to cause haemolysis. Doses of reserpine and hydrallazine used in this study are (moldered by the author to be comparable to those used in man. Since the intact experimental animal or man is more sensitive than the isolated tissue or organ, the slightly higher doses used in some experiments on isolated tissues do in fact approximate to the therapeutic dose levels. It is finally suggested that interference by these drugs with tissue metabolism may result in a decreased availability of energy for muscular contraction. It is postulated that hydrallazine Produces an "anoxia-like" condition in smooth muscle, while in oxidative phosphorylation, reserpine acts as an "uncoupling agent". Such an effect may explain the reduction of inherent tone in vascular smooth muscle and is probably responsible for the lowering of blood pressure
SETTING UP A MENTAL HEALTH CLINIC IN THE HEART OF RURAL AFRICA
Introduction: The World Health Organization defines health as a state of complete physical, mental and social well-being and
not merely the absence of disease or infirmity (WHO 1948). In Africa, mental health issues often come last on the list of priorities for
policy-makers& people’s attitudes towards mental illness are strongly influenced by traditional beliefs in supernatural
causes/remedies. The massive burden attributed to mental illness in these communities, poses a huge moral, cultural/economic
challenge and requires a concerted and integrated approach involving policy makers, mental health Practitioners, the general
public, service users and their families and other stake holders to reverse the trend.
Project Objectives:
• Improving community awareness of mental illness.
• Change the negative perception of mental illness by the community.
• Providing a screening/referral pathway for mental illnesses.
• Providing supervision of patient care.
Potential Results: Promote community participation on issues regarding mental health with a view to challenge existing
traditional attitudes and beliefs, reduce stigma and promote health seeking behaviour
PHP76 Evidence Requirements for Pricing and Reimbursement Decision Making for Orphan Drugs in Asia
Detection of internal N7-methylguanosine (m<sup>7</sup>G) RNA modifications by mutational profiling sequencing
Relativistic effects on the nuclear magnetic shielding tensor
A new approach for calculating relativistic corrections to the nuclear magnetic shieldings is presented. Starting from a full relativistic second order perturbation theory expression a two-component formalism is constructed by transforming matrix elements using the elimination of small component scheme and separating out the contributions from the no-virtual pair and the virtual pair part of the second order corrections to the energy. In this way we avoid a strong simplification used previously in the literature. We arrive at final expressions for the relativistic corrections which are equivalent to those of Fukui et al. J. Chem Phys. 105, 3175 (1996) and at some other additional terms correcting both the paramagnetic and the diamagnetic part of the nuclear magnetic shielding. Results for some relativistic corrections to the shieldings of the heavy and light nuclei in HX and CHȝX (X=Br,I) at both random phase and second order polarization propagator approach levels are given.Fil: Melo, Juan Ignacio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Física de Buenos Aires. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Física de Buenos Aires; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Física; ArgentinaFil: Ruiz de Azua, Martín César. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Física; ArgentinaFil: Giribet, Claudia Gloria. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Física; ArgentinaFil: Aucar, Gustavo Adolfo. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura. Departamento de Física; ArgentinaFil: Romero, Rodolfo Horacio. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura. Departamento de Física; Argentin
Sodium-tolerant matrix for matrix-assisted laser desorption/ionization mass spectrometry and post-source decay of oligonucleotides
International audienc
The tylosin resistance gene tlrB of Streptomyces fradiae encodes a methyltransferase that targets G748 in 23S rRNA
Metals in Catalysis, Biomimetics & Inorganic Material
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