CARBONIC anhydrase catalyses hydration of aldehydes1–3: illustration I have studied the relevance of hydration of glyceraldehyde-3-phosphate (GAP) in its oxidation by GAP dehydrogenase. GAP dehydrogenase activity was assayed spectrophotometrically by measuring the increase in absorbance at 340 nM of a reaction mixture containing 0.1 M Tris-HCl (pH 8.5), 17 mM sodium arsenate, 5 mM cysteine, 20 mM NaF, 1 mM NAD, 0.1 U/ml. of GAP dehydrogenase (Sigma) and 4 µM GAP.
REDUCED glutathione (GHS) is maintained in substantial concentration (3 × 10?3 M) within neurones1. The availability of new thiol-oxidizing agents like diamide2,3, which freely enter cells and the principal action of which is to reduce the GSH concentration by conversion to GSSG (equation 1), promoted an investigation of the effects of these agents on release of transmitter at frog myoneural junctions. illustration
IT has been reported1 that washed human platelets incubated with 14C-labelled cytidine monophpsphate-N-acetyl sialic acid (CMP-NANA) in the presence of homogenized rat liver as the source of sialyltransferase showed an increase in the amount of sialic acid bound to the platelet membrane: illustration
IT has been shown that rabbit anti-serum against rat serum (RARS) injected intravenously into rats produces fatal anaphylactic shock1. This was interpreted as a reaction of RARS with γ-globulins adsorbed on the cell surface2. It therefore seemed reasonable to investigate the same effect on enhancing antibodies by injecting RARS into rats bearing Yoshida ascites sarcoma (YAS). The result was as expected–delayed death. It has been suggested that the “de-enhanced” tumour cells become more susceptible to lymphocytes3. Although the presence of enhancing antibodies coating YAS cells has not actually been shown, if they are responsible for the observed phenomena, other agents acting on γ-globulins should result in both anaphylaxis and “de-enhancement”. We therefore used cathepsins isolated from white blood cells, which act specifically on β and γ-globulins4. illustration
THE carboxy-terminal tetrapeptide of gastrin, Trp-Met-Asp-Phe-NH2, has the same biological activity as the parent hormone1. Morley2,3 showed that certain substitutions in the Trp, Met and Phe positions gave active analogues and concluded that these positions are concerned only with binding at the site of action. In contrast, the only substitution in aspartic acid that gave activity was tetrazolyl for the β-carboxyl, thereby maintaining a proton donor of similar size at this position. Morley concluded that the aspartyl residue has a functional rather than a binding role and presumably is indispensable. The carboxy-terminal octapeptide of cholecystokinin (OP-CCK) contains the carboxy-terminal tetrapeptide of gastrin and has gastrin-like activity4. We report here that the synthetic analogue of OP-CCK, in which alanyl is substituted for aspartyl at the position in question illustration, stimulates gastric acid secretion. In conscious cats with gastric fistulas5, dose-response curves were established for gastric acid response to OP-CCK, 7-Ala OP-CCK and pentagastrin6. The peptides were given by continuous intravenous infusion and response is taken as peak 10 min output during a 30 min infusion at each dose level (Fig. 1). Assigning a potency of 1 to OP-CCK the relative molar potency of 7-Ala OP-CCK is about 1/110 and of pentagastrin is about 1/4. We also tested the analogue of gastrin tetrapeptide in which alanyl is substituted for aspartyl illustration and found no detectable stimulation of acid secretion at doses as high as 15 mg/kg h, confirming similar negative findings by Morley2 in rat. This suggests that the weak action of alanyl substituted analogues cannot readily be detected without the enhancement of potency conferred by the sulphated tyrosyl of OP-CCK7. Ondetti et al.7 showed that 7-Ala OP-CCK contracts guinea-pig gallbladder with a potency about 1/150th that of OP-CCK, comparable with that reported here for acid secretion. This suggests that the same part or parts of the molecule are required for cholecystokinetic action and for gastric secretory action; the aspartyl residue in the penultimate position is dispensable for both of these actions. On the assumption that gastrin and CCK act at the same site8, we propose that the corresponding aspartyl residue of gastrin is similarly dispensable. For a direct test of this hypothesis, studies are needed of the synthetic analogue in which alanyl is substituted for the penultimate aspartyl in gastrin hepta-decapeptide, perferably gastrin II with sulphated tyrosyl because it is more potent than gastrin I in certain species9.
THE molecular mechanism for initiating DNA replication can be studied using a subcellular system. Rao and Johnson1 found that HeLa cells in the pre-DNA-synthetic (G-1) period of the cell cycle initiate DNA synthesis after fusion with cells that are in the DNA synthetic (S) period. A previous subcellular system of DNA replication from HeLa cells2–4 consisted of intact nuclei, supplemented with the four deoxy-nucleoside triphosphates, salt, ATP and a cytosol factor. The nuclei in this system appeared to be permeable to proteins and DNA synthesis was very similar to that within intact cells. We report here the initiation of DNA synthesis in nuclei isolated from HeLa cells. Our results suggest that, with the synchronization method used, a small percentage of dormant G-1 nuclei can be stimulated by S-phase cytoplasm; this would be the case if the cells were receptive to stimulation for only 30–60 min during the cell cycle. illustration
ATMOSPHERIC oxygen is not in equilibrium with sea water with respect to the isotope exchange illustration but has an 18O excess of about 22‰ compared to sea water1. This could be due to isotope fractionation during respiration2. Another large contribution to the effect has been overlooked up to now. Photosynthesis on land takes place in transpiring leaves, where the difference in the vapour pressure of 16OH2 and 18OH2 concentrates the heavy molecules in their stationary water content. Since the free oxygen stems from the water in which photosynthesis takes place3–8 (with only a very small shift in isotopic composition9), photosynthesis on land is an 18O source for atmospheric O2. We have begun to study this effect quantitatively.
USEFUL antisera specific for thymocytes and peripheral T lymphocytes have only been widely available in the form of antisera to thymic isoantigens of the mouse1. We describe here the preparation and properties of a heterologous antiserum to guinea-pig thymocytes which is rendered specific for T lymphocytes after absorption with a pure population of B lymphocytes. We have already described2,3 the properties of the transplantable acute lymphatic leukaemia L2C of inbred strain two guinea-pigs. The L2C leukaemia cell is characterized as a B cell by the presence of surface immunoglobulin of the λ2 class, the secretion of a small amount of λ2 immunoglobulin and the presence of a receptor for antigen-antibody-complement (C3) complexes characteristic of the B cell population4. Because, as will be shown, the antiserum is specific both for thymocytes and thymus derived lymphocytes, it will be referred to as anti-thymus derived cell (anti-TDC) serum. The availability of such an antiserum for a species in which the in vivo and in vitro manifestations of delayed hyper-sensitivity are so easily demonstrated may prove to be highly advantageous. illustration
THE ribonuclease, barnase, produced by Bacillus amyloliquefaciens has a molecular weight of 12,382, consisting of 110 amino-acid residues. It is one of the smallest proteins containing neither disulphide bonds nor non-peptide cross-Bnks which nevertheless maintain a well defined tertiary structure1,2. The next smallest reported enzyme of similar nature is the lysozyme of phage T4, with 160 residues. The barnase structure is reversibly destroyed by denaturing solvents or heat2, in what approximates a one step, highly cooperative, transition. Studies of this reaction should be very useful in illustration approaching the general problem of sequence-determined folding in proteins. In particular, thermodynamically meaningful quantitative differences in the stability of various genetic variants and chemically modified, or synthetic, barnases could be measured. Some work has been reported on the effect of various environmental parameters on the transition3 as well as the effects of modification by carboxypeptidases4. Full utilization of such data requires knowledge of both amino-acid sequence and three dimensional structurs. The complete amino-acid sequence is reported here (Fig. 1). The sequence was obtained by conventional procedures involving analysis of peptides isolated after hydrolysis of the native or modified protein by various proteases.
正Dear Editor,Infectious bursal disease virus(IBDV)causes infectious bursal disease,a highly contagious immunosuppressive disease that affects young chickens and causes economic losses in the poultry industry worldwide.IBDV replicates mainly in actively dividing B lymphocytes within the bursa of Fabricius(BF),leading to immunosuppression in affected flocks(Mahgoub et al.,2012).Viral protein 2(VP2),the only structural component of the IBDV 相似文献
<正>Dear Editor,Severe fever with thrombocytopenia syndrome virus(SFTSV)is a newly identified viral pathogen of the genus Phlebovirus in the family Bunyaviridae(Sun et al.,2012).SFTSV was first identified from patient serum samples in China(Li et al.,2013;Ning et al.,2015).SFTSV can cause a severe hemorrhagic fever-like disease with a reported case fatality rate ranging from 2.5% 相似文献
<正>Dear Editor,Acute flaccid paralysis(AFP)is a complex syndrome often caused by polioviruses.While most countries have eradicated wild polioviruses by vaccination,AFP still remains a health problem in these countries.Most studies have highlighted non-polio enteroviruses(NPEVs)as 相似文献
Functional classification of proteins is central to comparative genomics. The need for algorithms tuned to enable integrative interpretation of analytical data is felt globally. The availability of a general, automated software with built-in flexibility will significantly aid this activity. We have prepared ARC (Automated Resource Classifier), which is an open source software meeting the user requirements of flexibility. The default classification scheme based on keyword match is agglomerative and directs entries into any of the 7 basic non-overlapping functional classes: Cell wall, Cell membrane and Transporters (C), Cell division (
). The keyword library of ARC was built serially by first drawing keywords from Bacillus subtilis and Escherichia coli K12. In subsequent steps, this library was further enriched by collecting terms from archaeal representative Archaeoglobus fulgidus, Gene Ontology, and Gene Symbols. ARC is 94.04% successful on 6,75,663 annotated proteins from 348 prokaryotes. Three examples are provided to illuminate the current perspectives on mycobacterial physiology and costs of proteins in 333 prokaryotes. ARC is available at http://arc.igib.res.in.
In this work, through a docking analysis of compounds from the ZINC chemical library on human β-tubulin using high performance computer cluster, we report new polycyclic aromatic compounds that bind with high energy on the colchicine binding site of β-tubulin, suggesting three new key amino acids. However, molecular dynamic analysis showed low stability in the interaction between ligand and receptor. Results were confirmed experimentally in in vitro and in vivo models that suggest that molecular dynamics simulation is the best option to find new potential β-tubulin inhibitors.
A DNA enzyme with peroxidase activity is a G-quadruplex-based DNAzyme formed by hemin and G-quadruplex DNA. Activity of peroxide DNAzymes can be influenced by the structure of quadruplex DNA. In this investigation, the interaction of hemin with T30695 G-quadruplex DNA is evaluated. Molecular dynamic simulation indicates that the binding mode of hemin to G-quadruplex DNA is end-stacking, which is consistent with absorption spectroscopy. Based on fluorescence spectroscopy, hemin ejects thiazole orange from bases of four-strand DNA. Circular dichroism spectra showed that no alteration occurs in this type of DNA structure.
The present paper reports the analysis of surface decoration on the structural, electronic, and optical properties of (n,0) ZnO nanotubes, performed by means of a density function theory based ab-initio approach. Fe functionalization induced buckling in ZnO nanotubes affects its electronic and optical properties. Increase in Fe functionalization leads to better stability of ZnO nanotube and shows enhanced metallic character. The possibility of its use in optoelectronics has been analyzed in terms of dielectric constant, absorption coefficient, and refractive index. In another observation, the high sensitivity of the HCN molecule for the Fe-incorporated ZnO nanotube suggests it as a potential gas sensor.
<正>Dear Editor,Hepatitis C virus(HCV)is a major cause of chronic liver diseases and hepatocellular carcinoma(HCC)with about71 million people globally infected.HCV encodes only10 viral proteins and its replication relies on host proteins.Many host factors including ADP-ribosylation factors 相似文献
