Interaction of diphtheria toxin fragment A and of elongation factor 2 with Cibacron blue

Diphtheria toxin fragment A interacts with Cibacron blue in solution, although it is not retained by blue Sepharose columns. Difference spectral titration of fragment A with the dye gives a dissociation constant of the order of 10^–5 M and a 11 stoichiometry for the complex. In equilibrium dialysis experiments Cibacron blue behaves as a competitive inhibitor of the binding of NAD to diphtheria toxin fragment A. The dye inhibits in a non-competitive way the fragment A-catalysed transfer of ADP-ribose from NAD to elongation factor 2 (EF2). By affinity chromatography on blue Sepharose a binding of EF2 and of ADP-ribosyl-EF2 with the dye is also demonstrated. GDP, GTP and GDP(CH₂)P are able to displace EF2 from blue Sepharose.     

Hydrolysis and protection from hydrolysis of enkephalins in human plasma

Seven groups of enkephalin-degrading enzymes and three groups of inhibitors active on these enzymes were separated from human plasma. The activity of the enzymes in hydrolyzing enkephalins and of the inhibitors in protecting enkephalins from proteolysis was measured. Results obtained with the endogenous inhibitors were compared to those relative to synthetic inhibitors. Data obtained indicate that all enkephalin-degrading enzymes found in plasma are significantly inhibited by the endogenous substances present in this tissue. The inhibition of the different classes of plasma enzymes by two of the three groups of endogenous substances is quite uniform, while one group of inhibitors appears specific to dipeptidylpeptidases. Results obtained are discussed in terms of the functional role of the inhibitory substances and of the possible pharmacological implication of their presence in human plasma.     

Binding of nicotinamide–adenine dinucleotides to diphtheria toxin

1. Changes in protein fluorescence have been utilized in determining the stoicheiometry and dissociation constants of the complexes of diphtheria toxin with NADH(2), NAD, NADPH(2) and NADP. 2. The binding stoicheiometry is 2moles of NADH(2) and 1mole of NADPH(2)/mole of diphtheria toxin. The binding sites for NADH(2) appear to be equivalent and independent. 3. The toxin shows a higher affinity for the reduced than for the oxidized forms of the nucleotides. 4. Dissociation constants at 0.01I, pH7 and 25 degrees are 0.7x10(-6)m for NADH(2) and 0.45x10(-6)m for NADPH(2). Dissociation constants increase with increasing ionic strength, indicating that the binding is mainly electrostatic. 5. Bound NADH(2) and NADPH(2) may be activated to fluoresce by the transfer of energy from the excited aromatic amino acids of the toxin. Activation and emission spectra of bound and free nucleotides are compared. 6. Since NAD and NADH(2) are cofactors specifically required for the inhibition of protein synthesis by diphtheria toxin, the possible role of toxin-nucleotide complexes is discussed in this regard.     

The diversity and evolution of recruitment behaviour in ants,with a discussion of the usefulness of parsimony criteria in the reconstruction of evolutionary histories

Summary Three alternative hypotheses about the evolution of recruitment behaviour in ants, based on accounts in the literature, are compared by means of a cladistic analysis. The three hypotheses are the following:Hypothesis 1. Increasingly efficient recruitment behaviours exhibited by different ant species have been shaped by or are correlated with ant phylogeny.Hypothesis 2. Increasingly efficient recruitment behaviours represent necessary evolutionary steps independently followed during the evolution of different ant clades.Hypothesis 3. Differently efficient recruitment behaviours have been selected in a convergent way among different species by similar population/environmental constraints.In a first stage of the analysis, these hypotheses have been compared in terms of parsimony (i.e. in terms of tree length = TL) of alternative cladograms based on recruitment behaviour only. The analysis gave the following results: Hypothesis 1, TL = 4; Hypothesis 2, TL = 18; Hypothesis 3, TL = 11. At least in terms of parsimony, hence, Hypothesis 1 appears to be the best. This hypothesis, however, cannot be retained for its total lack of congruence with current views on ant phylogeny. Among the remaining two hypotheses, Hypothesis 3 is again much (ca. 40%) more parsimonious than Hypothesis 2, but the retention index for recruitment behaviour on the relative cladogram is 0.2 as compared with 0.7 for Hypothesis 2. Practically, this implies biologically very implausible behavioural evolution indicated by very improbable ancestors for the species included in the analysis. In the case of recruitment evolution the biological credibility of each hypothesis is inversely proportional to its parsimony.The three hypotheses on the evolution of recruitment behaviour are compared again taking into account the morphological and behavioural correlates of recruitment. The results confirm those obtained by simple cladistic analysis of behaviour alone, namely that an obligatory (i. e. neither reversible nor random) increase in recruitment efficiency has been repeatedly selected within different ant clades. Inclusion of the recruitment correlates allows, in addition, a more precise formulation of the implications of each hypothesis and a tentative test of two other alternatives deduced from the literature. Most papers dealing with recruitment assume this behaviour to be controlled by a single gland, while at least two experimental analyses show that more than one gland is likely to be involved as behavioural releaser. A cladistic approach allowed testing of the following two adaptational hypotheses: A) Synergic behavioural control by several glands, allowing shift of the dominant role from one gland to another. B) Single gland control, making improbable the replacement of one gland by another that performs the same function. The results of the analysis appear to favour alternative A slightly, though neither alternative results in implausible evolutionary paths.It is stressed that parsimony remains the sole decisional criterion when no other criteria are available but it can by no way be preferred to the slightest trace of biological common sense.     

Antiproliferative effects of heparin on normal and transformed NIH/3T3 fibroblasts.

We studied the effect of heparin on proliferation and signalling in normal NIH/3T3 fibroblasts, and in cells transformed by different oncogenes. Heparin inhibited the proliferation of normal as well as of v-sis and v-erbB transformed fibroblasts in the presence of serum, but failed to inhibit v-erbB-driven proliferation in serum-starved cultures; under these conditions, heparin inhibited by approximately 50% the proliferation of normal and v-sis- transformed cells. Heparin also inhibited PDGF-induced cell proliferation and inositol lipid turnover in v-sis transformants, but it did not affect PDGF mitogenic signalling in NIH/3T3 fibroblasts.     

Spontaneous Cell Fusion in Macrophage Cultures Expressing High Levels of the P2Z/P2X7 Receptor

Mouse and human macrophages express a plasma membrane receptor for extracellular ATP named P2Z/P2X₇. This molecule, recently cloned, is endowed with the intriguing property of forming an aqueous pore that allows transmembrane fluxes of hydrophylic molecules of molecular weight below 900. The physiological function of this receptor is unknown. In a previous study we reported experiments suggesting that the P2Z/P2X₇ receptor is involved in the formation of macrophage-derived multinucleated giant cells (MGCs; Falzoni, S., M. Munerati, D. Ferrari, S. Spisani, S. Moretti, and F. Di Virgilio. 1995. J. Clin. Invest. 95:1207– 1216). We have selected several clones of mouse J774 macrophages that are characterized by either high or low expression of the P2Z/P2X₇ receptor and named these clones P2Zhyper or P2Zhypo, respectively. P2Zhyper, but not P2Zhypo, cells grown to confluence in culture spontaneously fuse to form MGCs. As previously shown for human macrophages, fusion is inhibited by the P2Z/P2X₇ blocker oxidized ATP. MGCs die shortly after fusion through a dramatic process of cytoplasmic sepimentation followed by fragmentation. These observations support our previous hypothesis that the P2Z/P2X₇ receptor is involved in macrophage fusion.     

The Cd technique identifies a specific structure related to centromeric function

Summary The evidence that the Cd technique identifies the kinetochore was based on the finding that inactive centromeres are C-positive but Cd-negative. The identity between Cd-positivity and centromere function is now confirmed by the reverse procedure: a stable abnormal chromosome is consistently C-negative but Cd-positive at its single centromeric constriction. This demonstrates that the Cd dots are not a relic of C-banding but identify the active centromere.