Phosphatases reactivation

Castleman, W. L., D. L. Dungworth, and W. S. Tyler. Cytochemically detected alterations of lung acid phosphatase reactivity following ozone exposure. Lab. Invest. 29 310-319, 1973. 

Within many tissues the enzymatic activities of the pyruvate and branched chain oxoacid dehydrogenases complexes are controlled in part by a phosphorylation -dephosphorylation mechanism (see Eq. 17-9). Phosphorylation of the decarboxylase subunit by an ATP-dependent kinase produces an inactive phosphoenzyme. A phosphatase reactivates the dehydrogenase to complete the regulatory cycle (see Eq. 17-9 and associated discussion). The regulation is apparently accomplished, in part, by controlling the affinity of the protein for... 

Nowels K, Kent E, Rinsho K, Oyasu R. Prostate specific antigen and acid phosphatase-reactive cells in cystitis cystica and glandularis. Arch Pathol Lab Med. 1988 112 734-737. 

Wick MR, Swanson PE, Manivel JC. Placental-like alkaline phosphatase reactivity in human tumors an immunohistochemical study of 520 cases. Hum Pathol. 1987 18 946-954. 

PDH is controlled allosterically. It is inhibited by ATP, acetyl-CoA, and NADH. In addition, it is subject to control by phosphorylation. When PDH kinase phosphorylates PDH, it becomes inactive. Removing the phosphate with the PDH phosphatase reactivates it. 

Specificity of the assay depends on the specificity (cross-reactivity) of the antibodies. Of the known cyanobacterial toxins, only hepatotoxins are detected and are, therefore, able to be screened for by protein phosphatase inhibition. 

A number of allergens from both honey bee and vespid venoms have been cloned and expressed by either Escherichia coli or baculovirus-infected insect cells (table 1) phospholipase Aj [20], hyaluronidase [21], acid phosphatase [13] and Api m6 [14] from honey bee venom, as well as antigen 5 [22], phospholipase A and hyaluronidase [23] from vespid venom, and dipeptidylpeptidases from both bee and Vespula venoms [15, 16]. Their reactivity with human-specific IgE antibodies to the respective allergens has been documented [11-16, 22, 23] and their specificity is superior... 

Figure 7.18 Amine-containing dendrimers can be activated with epibromohydrin to result in the formation of reactive epoxy groups on the dendrimer surface. This reactive intermediate then can be used to conjugate with thiol-containing proteins, such as thiolated alkaline phosphatase. The reaction results in the formation of a thioether bond.

Alkaline Phosphatase Conjugation to Cystamine-Modified DNA Using Amine- and Sulfhydryl-Reactive Heterobifunctional Crosslinkers... 

Cambella and Antia [385] determined phosphonates in seawater by fractionation of the total phosphorus. The seawater sample was divided into two aliquots. The first was analysed for total phosphorus by the nitrate oxidation method capable of breaking down phosphonates, phosphate esters, nucleotides, and polyphosphates. The second aliquot was added to a suspension of bacterial (Escherichia coli) alkaline phosphatase enzyme, incubated for 2h at 37 °C and subjected to hot acid hydrolysis for 1 h. The resultant hot acid-enzyme sample was assayed for molybdate reactive phosphate which was estimated as the sum of enzyme hydrolysable phosphate and acid hydrolysable... 

A considerable number of transcription factors have reactive cysteine residues, which enable them to respond to the redox conditions in the cell. Since cadmium perturbs redox homeostasis, it can affect this class of transcription factors. If cadmium can displace the tetra-coordinate zinc atoms in zinc finger-containing transcription factors, it will affect them as well. Many of the pathways involving activation and inactivation of transcription factors involve kinases and phosphatases, themselves under the intricate control of calcium fluxes. It is therefore no surprise that cadmium will exert effects on the activity of transcription factors, the activation of proto-oncogenes, and thereby on gene expression (Figure 20.8i and i ). 

The commercial availability of certain toxin standards has allowed researchers to examine the physiological mechanisms of allelopathy by cyanobacteria. The best known examples are from studies on microcystins, which affect plants and aquatic algae by interfering with protein phosphatases in a manner similar to their effect on vertebrate enzymes (Babica et al. 2006). However, there is evidence that microcystins can also promote the formation of reactive oxygen species (ROS) in photoautotrophs, which can cause extensive damage to cellular membranes and enzymes (Babica et al. 2006 Leflaive and Ten-Hage 2007). 

Already in 1982, it was suggested that the intermediate chromium(V) state is involved in the carcinogenic process.9 Reactive Cr(V) and Cr(IV) intermediates may be harmful in many ways acting as tyrosine phosphatase inhibitors, or by forming organic radicals upon reaction with cellular reductants, which in turn can react with O2 and lead to reactive oxygen species.10 Reaction of chromium(VI) with... 

Liver injury is clinically defined as an increase of serum alanine amino transferase (ALT) levels of more than three times the upper limit of normal and a total bilirubin level of more than twice the upper limit of normal [4]. The clinical patterns of liver injury can be characterized as hepatocellular (with a predominant initial elevation of ALT), cholestatic (with an initial elevation of alkaline phosphatase) or mixed. The mechanisms of drug-induced hepatotoxicity include excessive generation of reactive metabolites, mitochondrial dysfunction, oxidative stress and inhibition of bile salt efflux protein [5]. Better understandings of these mechanisms in the past decades led to the development of assays and models suitable for studying such toxic mechanisms and for selecting better leads in the drug discovery stage. 

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